PMC:1942070 JSONTXT 24 Projects

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Id Subject Object Predicate Lexical cue
T212 0-7 NN denotes Protein
T1742 0-3731 CD denotes Protein kinase D enzymes are dispensable for proliferation, survival and antigen receptor-regulated NFκB activity in vertebrate B-cells Abstract To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. Most cell types express at least two PKD isoforms but PKD enzymes are especially highly expressed in haematopoietic cells, where they are activated in response to antigen receptors stimulation [2,3]. A conserved signalling pathway linking antigen receptors to PKDs involves the activation of PLCγ and the subsequent production of diacylglycerol (DAG) which stimulates classical and/or novel protein kinase Cs (PKC) that phosphorylate two key regulatory serine residues in the activation loop of PKD kinases [3–6]. The N-terminal regulatory region of PKD enzymes contains a DAG binding domain and direct binding of DAG also contributes to PKD1 activation [7] as well as regulating the spatial location of PKD enzymes within cells [8–12]. PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). In particular, PKDs have been widely linked to the activation of the NFκB transcription factor and in regulating cell survival during oxidative stress [17,21–23]. Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. An essential role for PKD enzymes in regulating class II histone deacetylases (HDACs), enzymes that repress MEF2-dependent gene transcription, has also been demonstrated [1,26–28]. To investigate the biological role of PKDs we have generated DT40 B cell lines that lack expression of one or more members of the PKD family [1], allowing us to investigate the function(s) of PKD isoforms following B cell antigen receptor (BCR) stimulation, as well addressing the issue of functional redundancy between the different PKD family members. Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. However, PKD-null DT40 B cells are viable and proliferate normally. Moreover, loss of the entire cellular pool of PKD does not critically affect oxidative stress responses in B cells nor do PKD kinases play an essential role in regulating NFκB transcriptional activity. Together, these findings reveal that in B lymphocytes, PKD kinases are not critical regulators of many of the cellular processes previously ascribed to them in other cellular systems. 2 Materials and methods 2.1
T1939 0-4124 CD denotes Protein kinase D enzymes are dispensable for proliferation, survival and antigen receptor-regulated NFκB activity in vertebrate B-cells Abstract To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. Most cell types express at least two PKD isoforms but PKD enzymes are especially highly expressed in haematopoietic cells, where they are activated in response to antigen receptors stimulation [2,3]. A conserved signalling pathway linking antigen receptors to PKDs involves the activation of PLCγ and the subsequent production of diacylglycerol (DAG) which stimulates classical and/or novel protein kinase Cs (PKC) that phosphorylate two key regulatory serine residues in the activation loop of PKD kinases [3–6]. The N-terminal regulatory region of PKD enzymes contains a DAG binding domain and direct binding of DAG also contributes to PKD1 activation [7] as well as regulating the spatial location of PKD enzymes within cells [8–12]. PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). In particular, PKDs have been widely linked to the activation of the NFκB transcription factor and in regulating cell survival during oxidative stress [17,21–23]. Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. An essential role for PKD enzymes in regulating class II histone deacetylases (HDACs), enzymes that repress MEF2-dependent gene transcription, has also been demonstrated [1,26–28]. To investigate the biological role of PKDs we have generated DT40 B cell lines that lack expression of one or more members of the PKD family [1], allowing us to investigate the function(s) of PKD isoforms following B cell antigen receptor (BCR) stimulation, as well addressing the issue of functional redundancy between the different PKD family members. Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. However, PKD-null DT40 B cells are viable and proliferate normally. Moreover, loss of the entire cellular pool of PKD does not critically affect oxidative stress responses in B cells nor do PKD kinases play an essential role in regulating NFκB transcriptional activity. Together, these findings reveal that in B lymphocytes, PKD kinases are not critical regulators of many of the cellular processes previously ascribed to them in other cellular systems. 2 Materials and methods 2.1 Cell culture, transient transfections and cell stimulation The generation, culture and activation of PKD1−/−, PKD3−/− and PKD1/3−/− knockout DT40 B cell lines have been described previously [1]. Cells were lysed and protein extracts were analysed in Western blotting experiments as previously described [1]. Chloramphenicol acetyl transferase assays have been described previously [29]. 2.2
T2730 0-4547 CD denotes Protein kinase D enzymes are dispensable for proliferation, survival and antigen receptor-regulated NFκB activity in vertebrate B-cells Abstract To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. Most cell types express at least two PKD isoforms but PKD enzymes are especially highly expressed in haematopoietic cells, where they are activated in response to antigen receptors stimulation [2,3]. A conserved signalling pathway linking antigen receptors to PKDs involves the activation of PLCγ and the subsequent production of diacylglycerol (DAG) which stimulates classical and/or novel protein kinase Cs (PKC) that phosphorylate two key regulatory serine residues in the activation loop of PKD kinases [3–6]. The N-terminal regulatory region of PKD enzymes contains a DAG binding domain and direct binding of DAG also contributes to PKD1 activation [7] as well as regulating the spatial location of PKD enzymes within cells [8–12]. PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). In particular, PKDs have been widely linked to the activation of the NFκB transcription factor and in regulating cell survival during oxidative stress [17,21–23]. Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. An essential role for PKD enzymes in regulating class II histone deacetylases (HDACs), enzymes that repress MEF2-dependent gene transcription, has also been demonstrated [1,26–28]. To investigate the biological role of PKDs we have generated DT40 B cell lines that lack expression of one or more members of the PKD family [1], allowing us to investigate the function(s) of PKD isoforms following B cell antigen receptor (BCR) stimulation, as well addressing the issue of functional redundancy between the different PKD family members. Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. However, PKD-null DT40 B cells are viable and proliferate normally. Moreover, loss of the entire cellular pool of PKD does not critically affect oxidative stress responses in B cells nor do PKD kinases play an essential role in regulating NFκB transcriptional activity. Together, these findings reveal that in B lymphocytes, PKD kinases are not critical regulators of many of the cellular processes previously ascribed to them in other cellular systems. 2 Materials and methods 2.1 Cell culture, transient transfections and cell stimulation The generation, culture and activation of PKD1−/−, PKD3−/− and PKD1/3−/− knockout DT40 B cell lines have been described previously [1]. Cells were lysed and protein extracts were analysed in Western blotting experiments as previously described [1]. Chloramphenicol acetyl transferase assays have been described previously [29]. 2.2 sIgM staining DT40 B cells (2 × 106 cells per point) were resuspended in 200 μl buffer (RPMI 1640 media, 1% foetal calf serum) containing anti-chicken M1 monoclonal antibody conjugated to FITC for 20 min on ice. The cells were washed twice and fluorescent intensity was analysed by flow cytometry. All results shown are representative of at two to four independent experiments unless otherwise indicated. 3 Results 3.1
T4217 0-6823 CD denotes Protein kinase D enzymes are dispensable for proliferation, survival and antigen receptor-regulated NFκB activity in vertebrate B-cells Abstract To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. Most cell types express at least two PKD isoforms but PKD enzymes are especially highly expressed in haematopoietic cells, where they are activated in response to antigen receptors stimulation [2,3]. A conserved signalling pathway linking antigen receptors to PKDs involves the activation of PLCγ and the subsequent production of diacylglycerol (DAG) which stimulates classical and/or novel protein kinase Cs (PKC) that phosphorylate two key regulatory serine residues in the activation loop of PKD kinases [3–6]. The N-terminal regulatory region of PKD enzymes contains a DAG binding domain and direct binding of DAG also contributes to PKD1 activation [7] as well as regulating the spatial location of PKD enzymes within cells [8–12]. PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). In particular, PKDs have been widely linked to the activation of the NFκB transcription factor and in regulating cell survival during oxidative stress [17,21–23]. Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. An essential role for PKD enzymes in regulating class II histone deacetylases (HDACs), enzymes that repress MEF2-dependent gene transcription, has also been demonstrated [1,26–28]. To investigate the biological role of PKDs we have generated DT40 B cell lines that lack expression of one or more members of the PKD family [1], allowing us to investigate the function(s) of PKD isoforms following B cell antigen receptor (BCR) stimulation, as well addressing the issue of functional redundancy between the different PKD family members. Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. However, PKD-null DT40 B cells are viable and proliferate normally. Moreover, loss of the entire cellular pool of PKD does not critically affect oxidative stress responses in B cells nor do PKD kinases play an essential role in regulating NFκB transcriptional activity. Together, these findings reveal that in B lymphocytes, PKD kinases are not critical regulators of many of the cellular processes previously ascribed to them in other cellular systems. 2 Materials and methods 2.1 Cell culture, transient transfections and cell stimulation The generation, culture and activation of PKD1−/−, PKD3−/− and PKD1/3−/− knockout DT40 B cell lines have been described previously [1]. Cells were lysed and protein extracts were analysed in Western blotting experiments as previously described [1]. Chloramphenicol acetyl transferase assays have been described previously [29]. 2.2 sIgM staining DT40 B cells (2 × 106 cells per point) were resuspended in 200 μl buffer (RPMI 1640 media, 1% foetal calf serum) containing anti-chicken M1 monoclonal antibody conjugated to FITC for 20 min on ice. The cells were washed twice and fluorescent intensity was analysed by flow cytometry. All results shown are representative of at two to four independent experiments unless otherwise indicated. 3 Results 3.1 Loss of HSP27 phosphorylation in DT40 B cells lacking expression of PKD family kinases DT40 B cells express two PKD isoforms, PKD1 and PKD3, and as previously described we have recently generated DT40 B cell lines that lack expression of either PKD1 or PKD3 or both enzymes [1]. In generating the double knockout cell lines we targeted the PKD1 loci in a PKD3−/− cell line that expressed a Flag-PKD3 transgene under the control of a doxycycline-inducible promoter. Hence, in the presence of doxycycline, Flag-PKD3 expression in PKD1/3 double knockout cells is comparable to endogenous PKD3 present in wild-type DT40 cells and removal of doxycycline from the culture media for 5 days results in a completely null PKD phenotype (Fig. 1A). Previously, we have demonstrated that phosphorylation and nuclear exclusion of class II histone deacetylases (HDACs) during BCR engagement is defective in PKD1/3−/− B cells and can restored upon re-expression of a single PKD isoform [1]. The small heat shock protein HSP27 has recently been proposed as a PKD1 substrate [24] and we accordingly assessed whether PKD-null DT40 cells have defective phosphorylation of HSP27 on serine 82, the proposed PKD1 substrate sequence. We initially investigated the regulation of HSP27 phosphorylation in single knockout DT40 B cells lacking either PKD1 or PKD3. As shown in Fig. 1B, activation of the BCR or treatment with the DAG-mimetic PdBu increased the levels of HSP27 phosphorylation at S82 in wild-type DT40 B cells. BCR and phorbol ester signals were also able to increase HSP27 phosphorylation in PKD1 or PKD3 single knockout DT40 B cells (Fig. 1B). However, BCR- and phorbol ester-induced phosphorylation of HSP27 on S82 was abolished in B cells that lacked both PKD1 and PKD3 (Fig. 1C). Significantly, doxycycline-induced expression of the Flag-PKD3 transgene in the double knockout cells was sufficient to restore normal regulation of HSP27 phosphorylation (Fig. 1C). In contrast, expression of a kinase-deficient PKD3 mutant protein in the double knockout cells was not able to restore BCR- or phorbol ester-induced HSP27 phosphorylation (Fig. 1D). Hence, PKD3 as well as PKD1 can regulate HSP27 phosphorylation and in DT40 B cells they are functionally redundant as HSP27 kinases. 3.2
T5768 0-8942 CD denotes Protein kinase D enzymes are dispensable for proliferation, survival and antigen receptor-regulated NFκB activity in vertebrate B-cells Abstract To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. Most cell types express at least two PKD isoforms but PKD enzymes are especially highly expressed in haematopoietic cells, where they are activated in response to antigen receptors stimulation [2,3]. A conserved signalling pathway linking antigen receptors to PKDs involves the activation of PLCγ and the subsequent production of diacylglycerol (DAG) which stimulates classical and/or novel protein kinase Cs (PKC) that phosphorylate two key regulatory serine residues in the activation loop of PKD kinases [3–6]. The N-terminal regulatory region of PKD enzymes contains a DAG binding domain and direct binding of DAG also contributes to PKD1 activation [7] as well as regulating the spatial location of PKD enzymes within cells [8–12]. PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). In particular, PKDs have been widely linked to the activation of the NFκB transcription factor and in regulating cell survival during oxidative stress [17,21–23]. Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. An essential role for PKD enzymes in regulating class II histone deacetylases (HDACs), enzymes that repress MEF2-dependent gene transcription, has also been demonstrated [1,26–28]. To investigate the biological role of PKDs we have generated DT40 B cell lines that lack expression of one or more members of the PKD family [1], allowing us to investigate the function(s) of PKD isoforms following B cell antigen receptor (BCR) stimulation, as well addressing the issue of functional redundancy between the different PKD family members. Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. However, PKD-null DT40 B cells are viable and proliferate normally. Moreover, loss of the entire cellular pool of PKD does not critically affect oxidative stress responses in B cells nor do PKD kinases play an essential role in regulating NFκB transcriptional activity. Together, these findings reveal that in B lymphocytes, PKD kinases are not critical regulators of many of the cellular processes previously ascribed to them in other cellular systems. 2 Materials and methods 2.1 Cell culture, transient transfections and cell stimulation The generation, culture and activation of PKD1−/−, PKD3−/− and PKD1/3−/− knockout DT40 B cell lines have been described previously [1]. Cells were lysed and protein extracts were analysed in Western blotting experiments as previously described [1]. Chloramphenicol acetyl transferase assays have been described previously [29]. 2.2 sIgM staining DT40 B cells (2 × 106 cells per point) were resuspended in 200 μl buffer (RPMI 1640 media, 1% foetal calf serum) containing anti-chicken M1 monoclonal antibody conjugated to FITC for 20 min on ice. The cells were washed twice and fluorescent intensity was analysed by flow cytometry. All results shown are representative of at two to four independent experiments unless otherwise indicated. 3 Results 3.1 Loss of HSP27 phosphorylation in DT40 B cells lacking expression of PKD family kinases DT40 B cells express two PKD isoforms, PKD1 and PKD3, and as previously described we have recently generated DT40 B cell lines that lack expression of either PKD1 or PKD3 or both enzymes [1]. In generating the double knockout cell lines we targeted the PKD1 loci in a PKD3−/− cell line that expressed a Flag-PKD3 transgene under the control of a doxycycline-inducible promoter. Hence, in the presence of doxycycline, Flag-PKD3 expression in PKD1/3 double knockout cells is comparable to endogenous PKD3 present in wild-type DT40 cells and removal of doxycycline from the culture media for 5 days results in a completely null PKD phenotype (Fig. 1A). Previously, we have demonstrated that phosphorylation and nuclear exclusion of class II histone deacetylases (HDACs) during BCR engagement is defective in PKD1/3−/− B cells and can restored upon re-expression of a single PKD isoform [1]. The small heat shock protein HSP27 has recently been proposed as a PKD1 substrate [24] and we accordingly assessed whether PKD-null DT40 cells have defective phosphorylation of HSP27 on serine 82, the proposed PKD1 substrate sequence. We initially investigated the regulation of HSP27 phosphorylation in single knockout DT40 B cells lacking either PKD1 or PKD3. As shown in Fig. 1B, activation of the BCR or treatment with the DAG-mimetic PdBu increased the levels of HSP27 phosphorylation at S82 in wild-type DT40 B cells. BCR and phorbol ester signals were also able to increase HSP27 phosphorylation in PKD1 or PKD3 single knockout DT40 B cells (Fig. 1B). However, BCR- and phorbol ester-induced phosphorylation of HSP27 on S82 was abolished in B cells that lacked both PKD1 and PKD3 (Fig. 1C). Significantly, doxycycline-induced expression of the Flag-PKD3 transgene in the double knockout cells was sufficient to restore normal regulation of HSP27 phosphorylation (Fig. 1C). In contrast, expression of a kinase-deficient PKD3 mutant protein in the double knockout cells was not able to restore BCR- or phorbol ester-induced HSP27 phosphorylation (Fig. 1D). Hence, PKD3 as well as PKD1 can regulate HSP27 phosphorylation and in DT40 B cells they are functionally redundant as HSP27 kinases. 3.2 Cellular proliferation and survival in DT40 B cells lacking expression of PKD family kinases PKD enzymes have previously been linked to the regulation of cell proliferation and survival (reviewed in [20]). To investigate the effect that loss of PKD kinases had on B cell survival and/or proliferation we cultured wild-type and PKD-null cells in the presence (PKD1/3−/−: Flag-PKD3+ve) or absence (PKD1/3−/−) of doxycycline and monitored exponential growth. As shown in Fig. 2A, PKD1/3−/− cells proliferated exponentially and re-expression of Flag-PKD3 in these cells had no impact on the rate of proliferation. Furthermore, the viability of PKD1/3−/− B cells during routine culturing was not significantly different from that of wild-type B cells (data not shown). It was noted that the population doubling time of PKD1/3−/− cells was slightly slower than that of wild type DT40 cells (12.7 ± 2.8 h versus 10.2 ± 0.4 h) but the failure of PKD3 re-expression to modify the proliferation rate of PKD1/3−/− cells suggests that these small differences were most likely the result of clonal variation and were not caused specifically by loss of PKD enzymes. Thus, PKD family enzymes are not essential for regulating basal survival and proliferation of DT40 B cells. PKD enzymes, specifically PKD1 and PKD2, have previously been linked to a protective role against oxidative stress-induced injury in 3T3 fibroblast, HeLa and epithelial cell lines [17,30–32]. We therefore addressed the role of PKD family kinases in regulating B cell survival in response to oxidative stress and other stress stimuli. As shown in Fig. 2B, loss of PKD1/3 expression had no significant impact on the survival of DT40 B cells in response to mitochondrial stress stimuli (H2O2 or serum deprivation); DNA damaging agents (etoposide or doxorubicin); ER pathway stress due to calcium overload (thapsigargin) or following prolonged treatment with phorbol esters or Trichostatin A, an inhibitor of class I/II HDACs. Thus, PKD kinases do not play an essential role in regulating B cell survival in response to a range of different stress stimuli. 3.3
T213 8-14 NN denotes kinase
T214 15-16 NNP denotes D
T215 17-24 NNS denotes enzymes
T216 25-28 VBP denotes are
T217 29-40 JJ denotes dispensable
T218 41-44 IN denotes for
T219 45-58 NN denotes proliferation
T220 58-59 , denotes ,
T221 60-68 NN denotes survival
T222 69-72 CC denotes and
T223 73-80 NN denotes antigen
T224 81-99 JJ denotes receptor-regulated
T225 100-104 NN denotes NFκB
T226 105-113 NN denotes activity
T227 114-116 IN denotes in
T228 117-127 JJ denotes vertebrate
T229 128-135 NNPS denotes B-cells
T230 147-149 TO denotes To
T231 150-161 VB denotes investigate
T232 162-165 DT denotes the
T233 166-176 NN denotes importance
T234 177-179 IN denotes of
T235 180-187 NN denotes protein
T236 188-194 NN denotes kinase
T237 195-196 NNP denotes D
T238 197-198 -LRB- denotes (
T239 198-201 NNP denotes PKD
T240 201-202 -RRB- denotes )
T241 203-210 VBZ denotes enzymes
T242 211-213 PRP denotes we
T243 214-223 VBD denotes generated
T244 224-225 DT denotes a
T245 226-234 NNP denotes PKD-null
T246 235-239 NNP denotes DT40
T7377 237-13173 JJ denotes 40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. Most cell types express at least two PKD isoforms but PKD enzymes are especially highly expressed in haematopoietic cells, where they are activated in response to antigen receptors stimulation [2,3]. A conserved signalling pathway linking antigen receptors to PKDs involves the activation of PLCγ and the subsequent production of diacylglycerol (DAG) which stimulates classical and/or novel protein kinase Cs (PKC) that phosphorylate two key regulatory serine residues in the activation loop of PKD kinases [3–6]. The N-terminal regulatory region of PKD enzymes contains a DAG binding domain and direct binding of DAG also contributes to PKD1 activation [7] as well as regulating the spatial location of PKD enzymes within cells [8–12]. PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). In particular, PKDs have been widely linked to the activation of the NFκB transcription factor and in regulating cell survival during oxidative stress [17,21–23]. Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. An essential role for PKD enzymes in regulating class II histone deacetylases (HDACs), enzymes that repress MEF2-dependent gene transcription, has also been demonstrated [1,26–28]. To investigate the biological role of PKDs we have generated DT40 B cell lines that lack expression of one or more members of the PKD family [1], allowing us to investigate the function(s) of PKD isoforms following B cell antigen receptor (BCR) stimulation, as well addressing the issue of functional redundancy between the different PKD family members. Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. However, PKD-null DT40 B cells are viable and proliferate normally. Moreover, loss of the entire cellular pool of PKD does not critically affect oxidative stress responses in B cells nor do PKD kinases play an essential role in regulating NFκB transcriptional activity. Together, these findings reveal that in B lymphocytes, PKD kinases are not critical regulators of many of the cellular processes previously ascribed to them in other cellular systems. 2 Materials and methods 2.1 Cell culture, transient transfections and cell stimulation The generation, culture and activation of PKD1−/−, PKD3−/− and PKD1/3−/− knockout DT40 B cell lines have been described previously [1]. Cells were lysed and protein extracts were analysed in Western blotting experiments as previously described [1]. Chloramphenicol acetyl transferase assays have been described previously [29]. 2.2 sIgM staining DT40 B cells (2 × 106 cells per point) were resuspended in 200 μl buffer (RPMI 1640 media, 1% foetal calf serum) containing anti-chicken M1 monoclonal antibody conjugated to FITC for 20 min on ice. The cells were washed twice and fluorescent intensity was analysed by flow cytometry. All results shown are representative of at two to four independent experiments unless otherwise indicated. 3 Results 3.1 Loss of HSP27 phosphorylation in DT40 B cells lacking expression of PKD family kinases DT40 B cells express two PKD isoforms, PKD1 and PKD3, and as previously described we have recently generated DT40 B cell lines that lack expression of either PKD1 or PKD3 or both enzymes [1]. In generating the double knockout cell lines we targeted the PKD1 loci in a PKD3−/− cell line that expressed a Flag-PKD3 transgene under the control of a doxycycline-inducible promoter. Hence, in the presence of doxycycline, Flag-PKD3 expression in PKD1/3 double knockout cells is comparable to endogenous PKD3 present in wild-type DT40 cells and removal of doxycycline from the culture media for 5 days results in a completely null PKD phenotype (Fig. 1A). Previously, we have demonstrated that phosphorylation and nuclear exclusion of class II histone deacetylases (HDACs) during BCR engagement is defective in PKD1/3−/− B cells and can restored upon re-expression of a single PKD isoform [1]. The small heat shock protein HSP27 has recently been proposed as a PKD1 substrate [24] and we accordingly assessed whether PKD-null DT40 cells have defective phosphorylation of HSP27 on serine 82, the proposed PKD1 substrate sequence. We initially investigated the regulation of HSP27 phosphorylation in single knockout DT40 B cells lacking either PKD1 or PKD3. As shown in Fig. 1B, activation of the BCR or treatment with the DAG-mimetic PdBu increased the levels of HSP27 phosphorylation at S82 in wild-type DT40 B cells. BCR and phorbol ester signals were also able to increase HSP27 phosphorylation in PKD1 or PKD3 single knockout DT40 B cells (Fig. 1B). However, BCR- and phorbol ester-induced phosphorylation of HSP27 on S82 was abolished in B cells that lacked both PKD1 and PKD3 (Fig. 1C). Significantly, doxycycline-induced expression of the Flag-PKD3 transgene in the double knockout cells was sufficient to restore normal regulation of HSP27 phosphorylation (Fig. 1C). In contrast, expression of a kinase-deficient PKD3 mutant protein in the double knockout cells was not able to restore BCR- or phorbol ester-induced HSP27 phosphorylation (Fig. 1D). Hence, PKD3 as well as PKD1 can regulate HSP27 phosphorylation and in DT40 B cells they are functionally redundant as HSP27 kinases. 3.2 Cellular proliferation and survival in DT40 B cells lacking expression of PKD family kinases PKD enzymes have previously been linked to the regulation of cell proliferation and survival (reviewed in [20]). To investigate the effect that loss of PKD kinases had on B cell survival and/or proliferation we cultured wild-type and PKD-null cells in the presence (PKD1/3−/−: Flag-PKD3+ve) or absence (PKD1/3−/−) of doxycycline and monitored exponential growth. As shown in Fig. 2A, PKD1/3−/− cells proliferated exponentially and re-expression of Flag-PKD3 in these cells had no impact on the rate of proliferation. Furthermore, the viability of PKD1/3−/− B cells during routine culturing was not significantly different from that of wild-type B cells (data not shown). It was noted that the population doubling time of PKD1/3−/− cells was slightly slower than that of wild type DT40 cells (12.7 ± 2.8 h versus 10.2 ± 0.4 h) but the failure of PKD3 re-expression to modify the proliferation rate of PKD1/3−/− cells suggests that these small differences were most likely the result of clonal variation and were not caused specifically by loss of PKD enzymes. Thus, PKD family enzymes are not essential for regulating basal survival and proliferation of DT40 B cells. PKD enzymes, specifically PKD1 and PKD2, have previously been linked to a protective role against oxidative stress-induced injury in 3T3 fibroblast, HeLa and epithelial cell lines [17,30–32]. We therefore addressed the role of PKD family kinases in regulating B cell survival in response to oxidative stress and other stress stimuli. As shown in Fig. 2B, loss of PKD1/3 expression had no significant impact on the survival of DT40 B cells in response to mitochondrial stress stimuli (H2O2 or serum deprivation); DNA damaging agents (etoposide or doxorubicin); ER pathway stress due to calcium overload (thapsigargin) or following prolonged treatment with phorbol esters or Trichostatin A, an inhibitor of class I/II HDACs. Thus, PKD kinases do not play an essential role in regulating B cell survival in response to a range of different stress stimuli. 3.3 Antigen receptor regulated signalling pathways in PKD-null DT40 B cells To further explore the contribution of PKD kinases to DT40 B cell biology we investigated whether specific BCR-regulated signalling events were defective in the PKD-null B cells. Initial experiments revealed that surface expression of the BCR was reduced in PKD1/3−/− (and in PKD1/3−/−:Flag-PKD3+ve) cells compared to wild-type DT40 B cells (Fig. 3A and data not shown). Nevertheless, BCR-crosslinking of PKD1/3−/− cells was sufficient to induce the activation of a number of signalling cascades, similar to that observed in wild-type cells (Fig. 3B). Hence, BCR-induced activation of the Akt, mTOR/p70 S6 kinase (as shown by S6 ribosomal protein phosphorylation) and MAPK signalling pathways was clearly detectable in PKD1/3-null B cells (Fig. 3B). Furthermore, enhanced tyrosine phosphorylation of multiple cellular proteins as well as an increase in intracellular calcium levels was also observed following BCR stimulation of PKD1/3-null B cells (data not shown). We did observe that the strength of BCR (but not phorbol ester)-induced regulation of the Erk1-RSK1 signalling pathway was reduced in PKD1/3−/− B cells compared to wild-type B cells (Fig. 3B). One interpretation of this data is that PKD enzymes may modulate Erk activation. Indeed, PKD enzymes have previously been linked to the growth factor-regulated Erk signalling in fibroblast and endothelial cell lines [33–35]. However, BCR-induced Erk phosphorylation was also reduced in PKD1/3−/−-Flag-PKD3+ B cells (data not shown) suggesting that reduced BCR levels on the surface of PKD1/3−/− (and PKD1/3−/−-Flag-PKD3+) B cells may itself impact on the strength of activation of this specific intracellular signalling pathway. To search for other potential PKD targets that may show defective regulation in PKD1/3−/− DT40 B cells, we used a PKD substrate phospho-antibody that recognises consensus phosphorylation sequences targeted by PKD enzymes (LxRxxpS/T) [36]. As shown in Fig. 3C, phorbol ester- and BCR-induced phosphorylation of cellular substrates detected by this phospho-antibody was similar in wild-type and PKD1/3−/− cells and is therefore independent of PKD enzymes. However, pretreatment of both wild-type and PKD1/3−/− DT40 B cells with GF109203X, a bisindoylmaleimide derivative that inhibits PKCs prevented the induction of proteins that contain phosphorylated LxRxxS/T motifs. Thus loss of PKD1/3 enzymes does not globally disrupt the phosphorylation of cellular proteins that contain LxRxxpS/T motifs. This result is perhaps not surprising as LxRxxS/T motifs also act as good substrates for other serine/threonine kinases such as MAPKAPK2. However these experiments do provide further evidence that phosphospecific antisera are not sufficiently selective to be designated kinase specific substrate antisera. BCR-induced signalling pathways culminate in the activation of gene transcription events that control B cell survival, proliferation and function. In this context, it has been proposed that PKD family members control of gene transcription through activation of the NFκB transcription factor. Thus, PKD-mediated activation of NFκB occurs downstream of a variety of different signals, including mROS/oxidative stress, lysophosphatidic acid and the Bcr-Abl oncogene [17,21,23,30,37]. Furthermore, expression of an activated PKD1 mutant enhances HPK1-mediated NFκB activation [38]. In B cells, NFκB is known to be regulated via DAG and PKCβ [39,40] but whether PKDs are key intermediaries for NFκB regulation has not been explored. The data (Fig. 4A) show that NFκB transcriptional activity was strongly induced in both wild-type and PKD1/3−/− DT40 B cells in response to either phorbol ester or BCR stimulation. In contrast, BCR and phorbol ester-induced NFκB transcriptional activity was abolished in PKCβ−/− DT40 B cells (Fig. 4A), although strong activation of PKD kinases (as assessed by autophosphorylation of PKD1 at S916) was observed in the PKCβ−/− cells (Fig. 4B). Thus, PKD kinases are neither essential nor sufficient to mediate BCR-induced NFκB activation in DT40 B cells and hence do not participate in DAG/PKC mediated control of NFκB. 4 Discussion Protein
T247 240-252 NNP denotes B-lymphocyte
T248 253-257 NN denotes cell
T249 258-262 NN denotes line
T250 262-263 . denotes .
T251 264-274 RB denotes Previously
T252 275-277 PRP denotes we
T253 278-282 VBP denotes have
T254 283-288 VBN denotes shown
T255 289-293 IN denotes that
T256 294-298 NNS denotes PKDs
T257 299-303 VBP denotes have
T258 304-306 DT denotes an
T259 307-316 JJ denotes essential
T260 317-321 NN denotes role
T261 322-324 IN denotes in
T262 325-335 VBG denotes regulating
T263 336-341 NN denotes class
T264 342-344 NNP denotes II
T265 345-352 NN denotes histone
T266 353-365 NNS denotes deacetylases
T267 366-368 IN denotes in
T268 369-373 NNP denotes DT40
T269 374-381 NNPS denotes B-cells
T270 382-383 NNP denotes [
T271 383-391 NNP denotes Matthews
T272 391-392 , denotes ,
T273 393-397 NNP denotes S.A.
T274 397-398 , denotes ,
T275 399-402 NNP denotes Liu
T276 402-403 , denotes ,
T277 404-406 NNP denotes P.
T278 406-407 , denotes ,
T279 408-416 NNP denotes Spitaler
T280 416-417 , denotes ,
T281 418-420 NNP denotes M.
T282 420-421 , denotes ,
T283 422-427 NNP denotes Olson
T284 427-428 , denotes ,
T285 429-433 NNP denotes E.N.
T286 433-434 , denotes ,
T287 435-443 NNP denotes McKinsey
T288 443-444 , denotes ,
T289 445-449 NNP denotes T.A.
T290 449-450 , denotes ,
T291 451-459 NNP denotes Cantrell
T292 459-460 , denotes ,
T293 461-465 NNP denotes D.A.
T294 466-469 CC denotes and
T295 470-481 NNP denotes Scharenberg
T296 481-482 , denotes ,
T297 483-487 NNP denotes A.M.
T298 488-489 -LRB- denotes (
T299 489-493 CD denotes 2006
T300 493-494 -RRB- denotes )
T301 495-504 JJ denotes Essential
T302 505-509 NN denotes role
T303 510-513 IN denotes for
T304 514-521 NN denotes protein
T305 522-528 NN denotes kinase
T306 529-530 NNP denotes D
T307 531-537 NN denotes family
T308 538-545 NNS denotes kinases
T309 546-548 IN denotes in
T310 549-552 DT denotes the
T311 553-563 NN denotes regulation
T312 564-566 IN denotes of
T313 567-572 NN denotes class
T314 573-575 NNP denotes II
T315 576-583 NN denotes histone
T316 584-596 NNS denotes deacetylases
T317 597-599 IN denotes in
T318 600-601 NNP denotes B
T319 602-613 NNS denotes lymphocytes
T320 613-614 . denotes .
T321 615-618 NNP denotes Mol
T322 618-619 . denotes .
T323 620-624 NNP denotes Cell
T324 625-629 NNP denotes Biol
T325 629-630 . denotes .
T326 631-633 CD denotes 26
T327 633-634 , denotes ,
T328 635-639 CD denotes 1569
T1008 635-1057 JJ denotes 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The
T329 640-644 CD denotes 1577
T330 644-645 NNP denotes ]
T331 645-646 . denotes .
T332 647-649 PRP denotes We
T333 650-653 RB denotes now
T334 654-658 VBP denotes show
T335 659-663 IN denotes that
T336 664-668 NNS denotes PKDs
T337 669-672 VBP denotes are
T338 673-677 RB denotes also
T339 678-686 VBN denotes required
T340 687-689 TO denotes to
T341 690-698 VB denotes regulate
T342 699-704 NNP denotes HSP27
T343 705-720 NN denotes phosphorylation
T344 721-723 IN denotes in
T345 724-728 NNP denotes DT40
T346 729-736 NNPS denotes B-cells
T347 736-737 . denotes .
T348 738-745 RB denotes However
T349 745-746 , denotes ,
T350 747-749 IN denotes in
T351 750-758 NN denotes contrast
T352 759-761 TO denotes to
T353 762-770 JJ denotes previous
T354 771-783 NNS denotes observations
T355 784-786 IN denotes in
T356 787-792 JJ denotes other
T357 793-797 NN denotes cell
T358 798-803 NNS denotes types
T359 803-804 , denotes ,
T360 805-808 NNP denotes PKD
T361 809-816 VBZ denotes enzymes
T362 817-819 VB denotes do
T363 820-823 RB denotes not
T364 824-832 VB denotes regulate
T365 833-838 JJ denotes basic
T366 839-847 JJ denotes cellular
T367 848-857 NNS denotes processes
T368 858-862 JJ denotes such
T369 863-865 IN denotes as
T370 866-879 NN denotes proliferation
T371 880-882 CC denotes or
T372 883-891 NN denotes survival
T373 892-901 NNS denotes responses
T374 901-902 , denotes ,
T375 903-906 CC denotes nor
T376 907-911 NNP denotes NFκB
T377 912-927 JJ denotes transcriptional
T378 928-936 NN denotes activity
T379 937-947 JJ denotes downstream
T380 948-950 IN denotes of
T381 951-954 DT denotes the
T382 955-956 NNP denotes B
T383 957-961 NN denotes cell
T384 962-969 NN denotes antigen
T385 970-978 NN denotes receptor
T386 978-979 . denotes .
T387 980-984 RB denotes Thus
T388 984-985 , denotes ,
T389 986-990 NNS denotes PKDs
T390 991-995 VBP denotes have
T391 996-997 DT denotes a
T392 998-1007 JJ denotes selective
T393 1008-1012 NN denotes role
T394 1013-1015 IN denotes in
T395 1016-1020 NNP denotes DT40
T396 1021-1027 NNP denotes B-cell
T397 1028-1035 NN denotes biology
T398 1035-1036 . denotes .
T1009 1058-1065 NN denotes protein
T1010 1066-1072 NN denotes kinase
T1011 1073-1074 NNP denotes D
T1012 1075-1076 -LRB- denotes (
T1013 1076-1079 NNP denotes PKD
T1014 1079-1080 -RRB- denotes )
T1015 1081-1097 JJ denotes serine/threonine
T1016 1098-1104 NN denotes kinase
T1017 1105-1111 NN denotes family
T1018 1112-1115 VBZ denotes has
T1019 1116-1121 CD denotes three
T1020 1122-1129 NNS denotes members
T1021 1129-1130 : denotes :
T1022 1131-1135 NNP denotes PKD1
T1023 1135-1136 , denotes ,
T1024 1137-1141 NNP denotes PKD2
T1025 1142-1145 CC denotes and
T1026 1146-1150 NNP denotes PKD3
T1027 1150-1151 . denotes .
T1028 1152-1156 JJS denotes Most
T1029 1157-1161 NN denotes cell
T1030 1162-1167 NNS denotes types
T1031 1168-1175 VBP denotes express
T1032 1176-1178 IN denotes at
T1033 1179-1184 JJS denotes least
T1034 1185-1188 CD denotes two
T1035 1189-1192 NNP denotes PKD
T1036 1193-1201 NNS denotes isoforms
T1037 1202-1205 CC denotes but
T1038 1206-1209 NNP denotes PKD
T1039 1210-1217 NNS denotes enzymes
T1040 1218-1221 VBP denotes are
T1041 1222-1232 RB denotes especially
T1042 1233-1239 RB denotes highly
T1043 1240-1249 VBN denotes expressed
T1044 1250-1252 IN denotes in
T1045 1253-1267 JJ denotes haematopoietic
T1046 1268-1273 NNS denotes cells
T1047 1273-1274 , denotes ,
T1048 1275-1280 WRB denotes where
T1049 1281-1285 PRP denotes they
T1050 1286-1289 VBP denotes are
T1051 1290-1299 VBN denotes activated
T1052 1300-1302 IN denotes in
T1053 1303-1311 NN denotes response
T1054 1312-1314 TO denotes to
T1055 1315-1322 NN denotes antigen
T1056 1323-1332 NNS denotes receptors
T1057 1333-1344 NN denotes stimulation
T1058 1345-1346 NNP denotes [
T1059 1346-1349 CD denotes 2,3
T1060 1349-1350 NNP denotes ]
T1061 1350-1351 . denotes .
T1062 1352-1353 DT denotes A
T1063 1354-1363 JJ denotes conserved
T1064 1364-1374 JJ denotes signalling
T1065 1375-1382 NN denotes pathway
T1066 1383-1390 VBG denotes linking
T1067 1391-1398 NN denotes antigen
T1068 1399-1408 NNS denotes receptors
T1069 1409-1411 TO denotes to
T1070 1412-1416 NNS denotes PKDs
T1071 1417-1425 VBZ denotes involves
T1072 1426-1429 DT denotes the
T1073 1430-1440 NN denotes activation
T1074 1441-1443 IN denotes of
T1075 1444-1448 NNP denotes PLCγ
T1076 1449-1452 CC denotes and
T1077 1453-1456 DT denotes the
T1078 1457-1467 JJ denotes subsequent
T1079 1468-1478 NN denotes production
T1080 1479-1481 IN denotes of
T1081 1482-1496 NN denotes diacylglycerol
T1082 1497-1498 -LRB- denotes (
T1083 1498-1501 NNP denotes DAG
T1084 1501-1502 -RRB- denotes )
T1085 1503-1508 WDT denotes which
T1086 1509-1519 VBZ denotes stimulates
T1087 1520-1529 JJ denotes classical
T1088 1530-1536 CC denotes and/or
T1089 1537-1542 JJ denotes novel
T1090 1543-1550 NN denotes protein
T1091 1551-1557 NN denotes kinase
T1092 1558-1560 NNS denotes Cs
T1093 1561-1562 -LRB- denotes (
T1094 1562-1565 NNP denotes PKC
T1095 1565-1566 -RRB- denotes )
T1096 1567-1571 WDT denotes that
T1097 1572-1585 VBP denotes phosphorylate
T1098 1586-1589 CD denotes two
T1099 1590-1593 JJ denotes key
T1100 1594-1604 JJ denotes regulatory
T1101 1605-1611 NN denotes serine
T1102 1612-1620 NNS denotes residues
T1103 1621-1623 IN denotes in
T1104 1624-1627 DT denotes the
T1105 1628-1638 NN denotes activation
T1106 1639-1643 NN denotes loop
T1107 1644-1646 IN denotes of
T1108 1647-1650 NNP denotes PKD
T1109 1651-1658 VBZ denotes kinases
T1110 1659-1660 NNP denotes [
T1111 1660-1661 CD denotes 3
T1112 1662-1663 CD denotes 6
T1113 1663-1664 NNP denotes ]
T1114 1664-1665 . denotes .
T1115 1666-1669 DT denotes The
T1116 1670-1680 JJ denotes N-terminal
T1117 1681-1691 JJ denotes regulatory
T1118 1692-1698 NN denotes region
T1119 1699-1701 IN denotes of
T1120 1702-1705 NNP denotes PKD
T1121 1706-1713 VBZ denotes enzymes
T1122 1714-1722 VBZ denotes contains
T1123 1723-1724 DT denotes a
T1124 1725-1728 NNP denotes DAG
T1125 1729-1736 JJ denotes binding
T1126 1737-1743 NN denotes domain
T1127 1744-1747 CC denotes and
T1128 1748-1754 JJ denotes direct
T1129 1755-1762 JJ denotes binding
T1130 1763-1765 IN denotes of
T1131 1766-1769 NNP denotes DAG
T1132 1770-1774 RB denotes also
T1133 1775-1786 VBZ denotes contributes
T1134 1787-1789 TO denotes to
T1135 1790-1794 CD denotes PKD1
T1136 1795-1805 NN denotes activation
T1137 1806-1807 NN denotes [
T1138 1807-1808 CD denotes 7
T1139 1808-1809 NNP denotes ]
T1140 1810-1812 RB denotes as
T1141 1813-1817 RB denotes well
T1142 1818-1820 IN denotes as
T1143 1821-1831 VBG denotes regulating
T1144 1832-1835 DT denotes the
T1145 1836-1843 JJ denotes spatial
T1146 1844-1852 NN denotes location
T1147 1853-1855 IN denotes of
T1148 1856-1859 NNP denotes PKD
T1149 1860-1867 VBZ denotes enzymes
T1150 1868-1874 IN denotes within
T1151 1875-1880 NNS denotes cells
T1152 1881-1882 VBP denotes [
T1153 1882-1883 CD denotes 8
T1154 1884-1886 CD denotes 12
T1155 1886-1887 NN denotes ]
T1156 1887-1888 . denotes .
T1157 1889-1892 NNP denotes PKD
T1158 1893-1900 NNS denotes enzymes
T1159 1901-1905 VBP denotes have
T1160 1906-1910 VBN denotes been
T1161 1911-1919 VBN denotes proposed
T1162 1920-1922 TO denotes to
T1163 1923-1931 VB denotes regulate
T1164 1932-1940 JJ denotes numerous
T1165 1941-1949 JJ denotes cellular
T1166 1950-1959 NNS denotes functions
T1167 1959-1960 , denotes ,
T1168 1961-1970 VBG denotes including
T1169 1971-1975 NN denotes cell
T1170 1976-1989 NN denotes proliferation
T1171 1990-1991 NNP denotes [
T1172 1991-1993 CD denotes 13
T1173 1994-1996 CD denotes 16
T1174 1996-1997 NNP denotes ]
T1175 1997-1998 , denotes ,
T1176 1999-2013 JJ denotes anti-apoptotic
T1177 2014-2021 NNS denotes signals
T1178 2022-2023 NNP denotes [
T1179 2023-2028 CD denotes 17,18
T1180 2028-2029 NNP denotes ]
T1181 2030-2033 CC denotes and
T1182 2034-2043 JJ denotes thymocyte
T1183 2044-2055 NN denotes development
T1184 2056-2057 NNP denotes [
T1185 2057-2059 CD denotes 19
T1186 2059-2060 NNP denotes ]
T1187 2060-2061 . denotes .
T1188 2062-2072 NN denotes Expression
T1189 2073-2075 IN denotes of
T1190 2076-2082 JJ denotes mutant
T1191 2083-2096 RB denotes catalytically
T1192 2097-2105 JJ denotes inactive
T1193 2106-2109 CC denotes and
T1194 2110-2124 RB denotes constitutively
T1195 2125-2134 VBN denotes activated
T1196 2135-2139 NNS denotes PKDs
T1197 2140-2143 MD denotes can
T1198 2144-2148 RB denotes also
T1199 2149-2155 VB denotes modify
T1200 2156-2161 NNP denotes Golgi
T1201 2162-2170 NN denotes function
T1202 2170-2171 , denotes ,
T1203 2172-2176 NN denotes cell
T1204 2177-2185 NN denotes adhesion
T1205 2186-2189 CC denotes and
T1206 2190-2194 NN denotes cell
T1207 2195-2203 NN denotes motility
T1208 2204-2205 -LRB- denotes (
T1209 2205-2213 VBN denotes reviewed
T1210 2214-2216 IN denotes in
T1211 2217-2218 NNP denotes [
T1212 2218-2220 CD denotes 20
T1213 2220-2221 NNP denotes ]
T1214 2221-2222 -RRB- denotes )
T1215 2222-2223 . denotes .
T1216 2224-2226 IN denotes In
T1217 2227-2237 JJ denotes particular
T1218 2237-2238 , denotes ,
T1219 2239-2243 NNS denotes PKDs
T1220 2244-2248 VBP denotes have
T1221 2249-2253 VBN denotes been
T1222 2254-2260 RB denotes widely
T1223 2261-2267 VBN denotes linked
T1224 2268-2270 TO denotes to
T1225 2271-2274 DT denotes the
T1226 2275-2285 NN denotes activation
T1227 2286-2288 IN denotes of
T1228 2289-2292 DT denotes the
T1229 2293-2297 NNP denotes NFκB
T1230 2298-2311 NN denotes transcription
T1231 2312-2318 NN denotes factor
T1232 2319-2322 CC denotes and
T1233 2323-2325 IN denotes in
T1234 2326-2336 VBG denotes regulating
T1235 2337-2341 NN denotes cell
T1236 2342-2350 NN denotes survival
T1237 2351-2357 IN denotes during
T1238 2358-2367 JJ denotes oxidative
T1239 2368-2374 NN denotes stress
T1240 2375-2376 NNP denotes [
T1241 2376-2381 CD denotes 17,21
T1242 2382-2384 CD denotes 23
T1243 2384-2385 NNP denotes ]
T1244 2385-2386 . denotes .
T1245 2387-2394 DT denotes Another
T1246 2395-2403 RB denotes recently
T1247 2404-2412 VBN denotes proposed
T1248 2413-2417 NNP denotes PKD1
T1249 2418-2427 NN denotes substrate
T1250 2428-2430 VBZ denotes is
T1251 2431-2436 NNP denotes HSP27
T1252 2437-2438 NNP denotes [
T1253 2438-2440 CD denotes 24
T1254 2440-2441 NNP denotes ]
T1255 2441-2442 , denotes ,
T1256 2443-2444 DT denotes a
T1257 2445-2450 JJ denotes small
T1258 2451-2455 NN denotes heat
T1259 2456-2461 NN denotes shock
T1260 2462-2469 NN denotes protein
T1261 2470-2478 VBN denotes involved
T1262 2479-2481 IN denotes in
T1263 2482-2492 VBG denotes regulating
T1264 2493-2497 NN denotes cell
T1265 2498-2507 NN denotes migration
T1266 2508-2511 CC denotes and
T1267 2512-2516 NN denotes cell
T1268 2517-2525 NN denotes survival
T1269 2526-2527 NNP denotes [
T1270 2527-2529 CD denotes 25
T1271 2529-2530 NNP denotes ]
T1272 2530-2531 . denotes .
T1273 2532-2534 DT denotes An
T1274 2535-2544 JJ denotes essential
T1275 2545-2549 NN denotes role
T1276 2550-2553 IN denotes for
T1277 2554-2557 NNP denotes PKD
T1278 2558-2565 VBZ denotes enzymes
T1279 2566-2568 IN denotes in
T1280 2569-2579 VBG denotes regulating
T1281 2580-2585 NN denotes class
T1282 2586-2588 NNP denotes II
T1283 2589-2596 NN denotes histone
T1284 2597-2609 NNS denotes deacetylases
T1285 2610-2611 -LRB- denotes (
T1286 2611-2616 NNS denotes HDACs
T1287 2616-2617 -RRB- denotes )
T1288 2617-2618 , denotes ,
T1289 2619-2626 VBZ denotes enzymes
T1290 2627-2631 IN denotes that
T1291 2632-2639 VBZ denotes repress
T1292 2640-2654 JJ denotes MEF2-dependent
T1293 2655-2659 NN denotes gene
T1294 2660-2673 NN denotes transcription
T1295 2673-2674 , denotes ,
T1296 2675-2678 VBZ denotes has
T1297 2679-2683 RB denotes also
T1298 2684-2688 VBN denotes been
T1299 2689-2701 VBN denotes demonstrated
T1300 2702-2703 NNP denotes [
T1301 2703-2707 CD denotes 1,26
T1302 2708-2710 CD denotes 28
T1303 2710-2711 NN denotes ]
T1304 2711-2712 . denotes .
T1305 2713-2715 TO denotes To
T1306 2716-2727 VB denotes investigate
T1307 2728-2731 DT denotes the
T1308 2732-2742 JJ denotes biological
T1309 2743-2747 NN denotes role
T1310 2748-2750 IN denotes of
T1311 2751-2755 NNS denotes PKDs
T1312 2756-2758 PRP denotes we
T1313 2759-2763 VBP denotes have
T1314 2764-2773 VBN denotes generated
T1315 2774-2778 NNP denotes DT40
T1316 2779-2780 NNP denotes B
T1317 2781-2785 NN denotes cell
T1318 2786-2791 NNS denotes lines
T1319 2792-2796 WDT denotes that
T1320 2797-2801 VBP denotes lack
T1321 2802-2812 NN denotes expression
T1322 2813-2815 IN denotes of
T1323 2816-2819 CD denotes one
T1324 2820-2822 CC denotes or
T1325 2823-2827 JJR denotes more
T1326 2828-2835 NNS denotes members
T1327 2836-2838 IN denotes of
T1328 2839-2842 DT denotes the
T1329 2843-2846 NNP denotes PKD
T1330 2847-2853 NN denotes family
T1331 2854-2855 NNP denotes [
T1332 2855-2856 CD denotes 1
T1333 2856-2857 NNP denotes ]
T1334 2857-2858 , denotes ,
T1335 2859-2867 VBG denotes allowing
T1336 2868-2870 PRP denotes us
T1337 2871-2873 TO denotes to
T1338 2874-2885 VB denotes investigate
T1339 2886-2889 DT denotes the
T1340 2890-2898 NN denotes function
T1341 2898-2899 -LRB- denotes (
T1342 2899-2900 PRP denotes s
T1343 2900-2901 -RRB- denotes )
T1344 2902-2904 IN denotes of
T1345 2905-2908 NNP denotes PKD
T1346 2909-2917 VBZ denotes isoforms
T1347 2918-2927 VBG denotes following
T1348 2928-2929 NNP denotes B
T1349 2930-2934 NN denotes cell
T1350 2935-2942 NN denotes antigen
T1351 2943-2951 NN denotes receptor
T1352 2952-2953 -LRB- denotes (
T1353 2953-2956 NNP denotes BCR
T1354 2956-2957 -RRB- denotes )
T1355 2958-2969 NN denotes stimulation
T1356 2969-2970 , denotes ,
T1357 2971-2973 RB denotes as
T1358 2974-2978 RB denotes well
T1359 2979-2989 VBG denotes addressing
T1360 2990-2993 DT denotes the
T1361 2994-2999 NN denotes issue
T1362 3000-3002 IN denotes of
T1363 3003-3013 JJ denotes functional
T1364 3014-3024 NN denotes redundancy
T1365 3025-3032 IN denotes between
T1366 3033-3036 DT denotes the
T1367 3037-3046 JJ denotes different
T1368 3047-3050 NNP denotes PKD
T1369 3051-3057 NN denotes family
T1370 3058-3065 NNS denotes members
T1371 3065-3066 . denotes .
T1372 3067-3075 JJ denotes Previous
T1373 3076-3083 NNS denotes studies
T1374 3084-3088 VBP denotes have
T1375 3089-3094 VBN denotes shown
T1376 3095-3099 IN denotes that
T1377 3100-3104 NNS denotes PKDs
T1378 3105-3108 VBP denotes are
T1379 3109-3122 JJ denotes indispensable
T1380 3123-3126 IN denotes for
T1381 3127-3131 NNP denotes HDAC
T1382 3132-3142 NN denotes regulation
T1383 3143-3145 IN denotes in
T1384 3146-3147 NNP denotes B
T1385 3148-3153 NNS denotes cells
T1386 3154-3155 NNP denotes [
T1387 3155-3156 CD denotes 1
T1388 3156-3157 NNP denotes ]
T1389 3157-3158 . denotes .
T1390 3159-3165 NNP denotes Herein
T1391 3166-3168 PRP denotes we
T1392 3169-3173 VBP denotes show
T1393 3174-3178 IN denotes that
T1394 3179-3183 NNS denotes PKDs
T1395 3184-3187 VBP denotes are
T1396 3188-3192 RB denotes also
T1397 3193-3206 JJ denotes indispensable
T1398 3207-3210 IN denotes for
T1399 3211-3216 NNP denotes HSP27
T1400 3217-3232 NN denotes phosphorylation
T1401 3233-3235 IN denotes in
T1402 3236-3237 NNP denotes B
T1403 3238-3243 NNS denotes cells
T1404 3243-3244 . denotes .
T1405 3245-3252 RB denotes However
T1406 3252-3253 , denotes ,
T1407 3254-3262 NNP denotes PKD-null
T1408 3263-3267 NNP denotes DT40
T1409 3268-3269 NNP denotes B
T1410 3270-3275 NNS denotes cells
T1411 3276-3279 VBP denotes are
T1412 3280-3286 JJ denotes viable
T1413 3287-3290 CC denotes and
T1414 3291-3302 VB denotes proliferate
T1415 3303-3311 RB denotes normally
T1416 3311-3312 . denotes .
T1417 3313-3321 RB denotes Moreover
T1418 3321-3322 , denotes ,
T1419 3323-3327 NN denotes loss
T1420 3328-3330 IN denotes of
T1421 3331-3334 DT denotes the
T1422 3335-3341 JJ denotes entire
T1423 3342-3350 JJ denotes cellular
T1424 3351-3355 NN denotes pool
T1425 3356-3358 IN denotes of
T1426 3359-3362 NNP denotes PKD
T1427 3363-3367 VBZ denotes does
T1428 3368-3371 RB denotes not
T1429 3372-3382 RB denotes critically
T1430 3383-3389 VB denotes affect
T1431 3390-3399 JJ denotes oxidative
T1432 3400-3406 NN denotes stress
T1433 3407-3416 NNS denotes responses
T1434 3417-3419 IN denotes in
T1435 3420-3421 NNP denotes B
T1436 3422-3427 NNS denotes cells
T1437 3428-3431 CC denotes nor
T1438 3432-3434 VBP denotes do
T1439 3435-3438 NNP denotes PKD
T1440 3439-3446 VBZ denotes kinases
T1441 3447-3451 VB denotes play
T1442 3452-3454 DT denotes an
T1443 3455-3464 JJ denotes essential
T1444 3465-3469 NN denotes role
T1445 3470-3472 IN denotes in
T1446 3473-3483 VBG denotes regulating
T1447 3484-3488 NNP denotes NFκB
T1448 3489-3504 JJ denotes transcriptional
T1449 3505-3513 NN denotes activity
T1450 3513-3514 . denotes .
T1451 3515-3523 RB denotes Together
T1452 3523-3524 , denotes ,
T1453 3525-3530 DT denotes these
T1454 3531-3539 NNS denotes findings
T1455 3540-3546 VBP denotes reveal
T1456 3547-3551 IN denotes that
T1457 3552-3554 IN denotes in
T1458 3555-3556 NNP denotes B
T1459 3557-3568 NNS denotes lymphocytes
T1460 3568-3569 , denotes ,
T1461 3570-3573 NNP denotes PKD
T1462 3574-3581 NNS denotes kinases
T1463 3582-3585 VBP denotes are
T1464 3586-3589 RB denotes not
T1465 3590-3598 JJ denotes critical
T1466 3599-3609 NNS denotes regulators
T1467 3610-3612 IN denotes of
T1468 3613-3617 JJ denotes many
T1469 3618-3620 IN denotes of
T1470 3621-3624 DT denotes the
T1471 3625-3633 JJ denotes cellular
T1472 3634-3643 NNS denotes processes
T1473 3644-3654 RB denotes previously
T1474 3655-3663 VBD denotes ascribed
T1475 3664-3666 TO denotes to
T1476 3667-3671 PRP denotes them
T1477 3672-3674 IN denotes in
T1478 3675-3680 JJ denotes other
T1479 3681-3689 JJ denotes cellular
T1480 3690-3697 NNS denotes systems
T1481 3697-3698 . denotes .
T1743 3731-3735 NNP denotes Cell
T1744 3736-3743 NN denotes culture
T1745 3743-3744 , denotes ,
T1746 3745-3754 NN denotes transient
T1747 3755-3768 NNS denotes transfections
T1748 3769-3772 CC denotes and
T1749 3773-3777 NN denotes cell
T1750 3778-3789 NN denotes stimulation
T1751 3790-3793 DT denotes The
T1752 3794-3804 NN denotes generation
T1753 3804-3805 , denotes ,
T1754 3806-3813 NN denotes culture
T1755 3814-3817 CC denotes and
T1756 3818-3828 NN denotes activation
T1757 3829-3831 IN denotes of
T1758 3832-3836 CD denotes PKD1
T1759 3836-3837 CD denotes
T1760 3837-3838 NN denotes /
T1761 3838-3839 NN denotes
T1762 3839-3840 , denotes ,
T1763 3841-3845 NNP denotes PKD3
T1764 3845-3846 NNP denotes
T1765 3846-3847 VBD denotes /
T1766 3847-3848 CD denotes
T1767 3849-3852 CC denotes and
T1768 3853-3859 CD denotes PKD1/3
T1769 3859-3860 CD denotes
T1770 3860-3861 NN denotes /
T1771 3861-3862 NN denotes
T1772 3863-3871 NN denotes knockout
T1773 3872-3876 NNP denotes DT40
T1774 3877-3878 NNP denotes B
T1775 3879-3883 NN denotes cell
T1776 3884-3889 NNS denotes lines
T1777 3890-3894 VBP denotes have
T1778 3895-3899 VBN denotes been
T1779 3900-3909 VBN denotes described
T1780 3910-3920 RB denotes previously
T1781 3921-3922 NNP denotes [
T1782 3922-3923 CD denotes 1
T1783 3923-3924 NNP denotes ]
T1784 3924-3925 . denotes .
T1785 3926-3931 NNS denotes Cells
T1786 3932-3936 VBD denotes were
T1787 3937-3942 VBN denotes lysed
T1788 3943-3946 CC denotes and
T1789 3947-3954 NN denotes protein
T1790 3955-3963 NNS denotes extracts
T1791 3964-3968 VBD denotes were
T1792 3969-3977 VBN denotes analysed
T1793 3978-3980 IN denotes in
T1794 3981-3988 JJ denotes Western
T1795 3989-3997 VBG denotes blotting
T1796 3998-4009 NNS denotes experiments
T1797 4010-4012 IN denotes as
T1798 4013-4023 RB denotes previously
T1799 4024-4033 VBN denotes described
T1800 4034-4035 NNP denotes [
T1801 4035-4036 CD denotes 1
T1802 4036-4037 NNP denotes ]
T1803 4037-4038 . denotes .
T1804 4039-4054 NNP denotes Chloramphenicol
T1805 4055-4061 NN denotes acetyl
T1806 4062-4073 NN denotes transferase
T1807 4074-4080 NNS denotes assays
T1808 4081-4085 VBP denotes have
T1809 4086-4090 VBN denotes been
T1810 4091-4100 VBN denotes described
T1811 4101-4111 RB denotes previously
T1812 4112-4113 NNP denotes [
T1813 4113-4115 CD denotes 29
T1814 4115-4116 NNP denotes ]
T1815 4116-4117 . denotes .
T1940 4124-4128 JJ denotes sIgM
T1941 4129-4137 VBG denotes staining
T1942 4138-4142 NNP denotes DT40
T1943 4143-4144 NNP denotes B
T1944 4145-4150 NNS denotes cells
T1945 4151-4152 -LRB- denotes (
T1946 4152-4153 CD denotes 2
T1947 4154-4155 CD denotes ×
T1948 4156-4159 CD denotes 106
T1949 4160-4165 NNS denotes cells
T1950 4166-4169 IN denotes per
T1951 4170-4175 NN denotes point
T1952 4175-4176 -RRB- denotes )
T1953 4177-4181 VBD denotes were
T1954 4182-4193 VBN denotes resuspended
T1955 4194-4196 IN denotes in
T1956 4197-4200 CD denotes 200
T1957 4201-4203 NN denotes μl
T1958 4204-4210 NN denotes buffer
T1959 4211-4212 -LRB- denotes (
T1960 4212-4216 NNP denotes RPMI
T1961 4217-4221 CD denotes 1640
T1962 4222-4227 NNS denotes media
T1963 4227-4228 , denotes ,
T1964 4229-4230 CD denotes 1
T1965 4230-4231 NN denotes %
T1966 4232-4238 JJ denotes foetal
T1967 4239-4243 NN denotes calf
T1968 4244-4249 NN denotes serum
T1969 4249-4250 -RRB- denotes )
T1970 4251-4261 VBG denotes containing
T1971 4262-4274 JJ denotes anti-chicken
T1972 4275-4277 CD denotes M1
T1973 4278-4288 JJ denotes monoclonal
T1974 4289-4297 NN denotes antibody
T1975 4298-4308 VBN denotes conjugated
T1976 4309-4311 TO denotes to
T1977 4312-4316 NNP denotes FITC
T1978 4317-4320 IN denotes for
T1979 4321-4323 CD denotes 20
T1980 4324-4327 NN denotes min
T1981 4328-4330 IN denotes on
T1982 4331-4334 NN denotes ice
T1983 4334-4335 . denotes .
T1984 4336-4339 DT denotes The
T1985 4340-4345 NNS denotes cells
T1986 4346-4350 VBD denotes were
T1987 4351-4357 VBN denotes washed
T1988 4358-4363 RB denotes twice
T1989 4364-4367 CC denotes and
T1990 4368-4379 JJ denotes fluorescent
T1991 4380-4389 NN denotes intensity
T1992 4390-4393 VBD denotes was
T1993 4394-4402 VBN denotes analysed
T1994 4403-4405 IN denotes by
T1995 4406-4410 NN denotes flow
T1996 4411-4420 NN denotes cytometry
T1997 4420-4421 . denotes .
T1998 4422-4425 DT denotes All
T1999 4426-4433 NNS denotes results
T2000 4434-4439 VBN denotes shown
T2001 4440-4443 VBP denotes are
T2002 4444-4458 NN denotes representative
T2003 4459-4461 IN denotes of
T2004 4462-4464 IN denotes at
T2005 4465-4468 CD denotes two
T2006 4469-4471 TO denotes to
T2007 4472-4476 CD denotes four
T2008 4477-4488 JJ denotes independent
T2009 4489-4500 NNS denotes experiments
T2010 4501-4507 IN denotes unless
T2011 4508-4517 RB denotes otherwise
T2012 4518-4527 VBN denotes indicated
T2013 4527-4528 . denotes .
T2731 4547-4551 NN denotes Loss
T2732 4552-4554 IN denotes of
T2733 4555-4560 NNP denotes HSP27
T2734 4561-4576 NN denotes phosphorylation
T2735 4577-4579 IN denotes in
T2736 4580-4584 NNP denotes DT40
T2737 4585-4586 NNP denotes B
T2738 4587-4592 NNS denotes cells
T2739 4593-4600 VBG denotes lacking
T2740 4601-4611 NN denotes expression
T2741 4612-4614 IN denotes of
T2742 4615-4618 NNP denotes PKD
T2743 4619-4625 NN denotes family
T2744 4626-4633 VBZ denotes kinases
T2745 4634-4638 NNP denotes DT40
T2746 4639-4640 NNP denotes B
T2747 4641-4646 NNS denotes cells
T2748 4647-4654 VBP denotes express
T2749 4655-4658 CD denotes two
T2750 4659-4662 NNP denotes PKD
T2751 4663-4671 NNS denotes isoforms
T2752 4671-4672 , denotes ,
T2753 4673-4677 NNP denotes PKD1
T2754 4678-4681 CC denotes and
T2755 4682-4686 NNP denotes PKD3
T2756 4686-4687 , denotes ,
T2757 4688-4691 CC denotes and
T2758 4692-4694 IN denotes as
T2759 4695-4705 RB denotes previously
T2760 4706-4715 VBN denotes described
T2761 4716-4718 PRP denotes we
T2762 4719-4723 VBP denotes have
T2763 4724-4732 RB denotes recently
T2764 4733-4742 VBN denotes generated
T2765 4743-4747 NNP denotes DT40
T2766 4748-4749 NNP denotes B
T2767 4750-4754 NN denotes cell
T2768 4755-4760 NNS denotes lines
T2769 4761-4765 WDT denotes that
T2770 4766-4770 VBP denotes lack
T2771 4771-4781 NN denotes expression
T2772 4782-4784 IN denotes of
T2773 4785-4791 DT denotes either
T2774 4792-4796 CD denotes PKD1
T2775 4797-4799 CC denotes or
T2776 4800-4804 CD denotes PKD3
T2777 4805-4807 CC denotes or
T2778 4808-4812 DT denotes both
T2779 4813-4820 NNS denotes enzymes
T2780 4821-4822 VBP denotes [
T2781 4822-4823 CD denotes 1
T2782 4823-4824 NNP denotes ]
T2783 4824-4825 . denotes .
T2784 4826-4828 IN denotes In
T2785 4829-4839 VBG denotes generating
T2786 4840-4843 DT denotes the
T2787 4844-4850 JJ denotes double
T2788 4851-4859 NN denotes knockout
T2789 4860-4864 NN denotes cell
T2790 4865-4870 NNS denotes lines
T2791 4871-4873 PRP denotes we
T2792 4874-4882 VBD denotes targeted
T2793 4883-4886 DT denotes the
T2794 4887-4891 NNP denotes PKD1
T2795 4892-4896 NN denotes loci
T2796 4897-4899 IN denotes in
T2797 4900-4901 DT denotes a
T2798 4902-4906 NNP denotes PKD3
T2799 4906-4907 NNP denotes
T2800 4907-4908 VBD denotes /
T2801 4908-4909 CD denotes
T2802 4910-4914 NN denotes cell
T2803 4915-4919 NN denotes line
T2804 4920-4924 WDT denotes that
T2805 4925-4934 VBD denotes expressed
T2806 4935-4936 DT denotes a
T2807 4937-4946 NN denotes Flag-PKD3
T2808 4947-4956 NN denotes transgene
T2809 4957-4962 IN denotes under
T2810 4963-4966 DT denotes the
T2811 4967-4974 NN denotes control
T2812 4975-4977 IN denotes of
T2813 4978-4979 DT denotes a
T2814 4980-5001 JJ denotes doxycycline-inducible
T2815 5002-5010 NN denotes promoter
T2816 5010-5011 . denotes .
T2817 5012-5017 RB denotes Hence
T2818 5017-5018 , denotes ,
T2819 5019-5021 IN denotes in
T2820 5022-5025 DT denotes the
T2821 5026-5034 NN denotes presence
T2822 5035-5037 IN denotes of
T2823 5038-5049 NN denotes doxycycline
T2824 5049-5050 , denotes ,
T2825 5051-5060 NN denotes Flag-PKD3
T2826 5061-5071 NN denotes expression
T2827 5072-5074 IN denotes in
T2828 5075-5081 CD denotes PKD1/3
T2829 5082-5088 JJ denotes double
T2830 5089-5097 NN denotes knockout
T2831 5098-5103 NNS denotes cells
T2832 5104-5106 VBZ denotes is
T2833 5107-5117 JJ denotes comparable
T2834 5118-5120 TO denotes to
T2835 5121-5131 JJ denotes endogenous
T2836 5132-5136 JJ denotes PKD3
T2837 5137-5144 NN denotes present
T2838 5145-5147 IN denotes in
T2839 5148-5157 JJ denotes wild-type
T2840 5158-5162 NNP denotes DT40
T2841 5163-5168 NNS denotes cells
T2842 5169-5172 CC denotes and
T2843 5173-5180 NN denotes removal
T2844 5181-5183 IN denotes of
T2845 5184-5195 NN denotes doxycycline
T2846 5196-5200 IN denotes from
T2847 5201-5204 DT denotes the
T2848 5205-5212 NN denotes culture
T2849 5213-5218 NNS denotes media
T2850 5219-5222 IN denotes for
T2851 5223-5224 CD denotes 5
T2852 5225-5229 NNS denotes days
T2853 5230-5237 NNS denotes results
T2854 5238-5240 IN denotes in
T2855 5241-5242 DT denotes a
T2856 5243-5253 RB denotes completely
T2857 5254-5258 JJ denotes null
T2858 5259-5262 NNP denotes PKD
T2859 5263-5272 NN denotes phenotype
T2860 5273-5274 -LRB- denotes (
T2861 5274-5278 NNP denotes Fig.
T2862 5279-5281 NNP denotes 1A
T2863 5281-5282 -RRB- denotes )
T2864 5282-5283 . denotes .
T2865 5284-5294 RB denotes Previously
T2866 5294-5295 , denotes ,
T2867 5296-5298 PRP denotes we
T2868 5299-5303 VBP denotes have
T2869 5304-5316 VBN denotes demonstrated
T2870 5317-5321 IN denotes that
T2871 5322-5337 NN denotes phosphorylation
T2872 5338-5341 CC denotes and
T2873 5342-5349 JJ denotes nuclear
T2874 5350-5359 NN denotes exclusion
T2875 5360-5362 IN denotes of
T2876 5363-5368 NN denotes class
T2877 5369-5371 NNP denotes II
T2878 5372-5379 NN denotes histone
T2879 5380-5392 NNS denotes deacetylases
T2880 5393-5394 -LRB- denotes (
T2881 5394-5399 NNS denotes HDACs
T2882 5399-5400 -RRB- denotes )
T2883 5401-5407 IN denotes during
T2884 5408-5411 NNP denotes BCR
T2885 5412-5422 NN denotes engagement
T2886 5423-5425 VBZ denotes is
T2887 5426-5435 JJ denotes defective
T2888 5436-5438 IN denotes in
T2889 5439-5445 CD denotes PKD1/3
T2890 5445-5446 CD denotes
T2891 5446-5447 NN denotes /
T2892 5447-5448 NN denotes
T2893 5449-5450 NNP denotes B
T2894 5451-5456 NNS denotes cells
T2895 5457-5460 CC denotes and
T2896 5461-5464 MD denotes can
T2897 5465-5473 VBD denotes restored
T2898 5474-5478 IN denotes upon
T2899 5479-5492 NN denotes re-expression
T2900 5493-5495 IN denotes of
T2901 5496-5497 DT denotes a
T2902 5498-5504 JJ denotes single
T2903 5505-5508 NNP denotes PKD
T2904 5509-5516 NN denotes isoform
T2905 5517-5518 NNP denotes [
T2906 5518-5519 CD denotes 1
T2907 5519-5520 NNP denotes ]
T2908 5520-5521 . denotes .
T2909 5522-5525 DT denotes The
T2910 5526-5531 JJ denotes small
T2911 5532-5536 NN denotes heat
T2912 5537-5542 NN denotes shock
T2913 5543-5550 NN denotes protein
T2914 5551-5556 NNP denotes HSP27
T2915 5557-5560 VBZ denotes has
T2916 5561-5569 RB denotes recently
T2917 5570-5574 VBN denotes been
T2918 5575-5583 VBN denotes proposed
T2919 5584-5586 IN denotes as
T2920 5587-5588 DT denotes a
T2921 5589-5593 NNP denotes PKD1
T2922 5594-5603 VB denotes substrate
T2923 5604-5605 NNP denotes [
T2924 5605-5607 CD denotes 24
T2925 5607-5608 NNP denotes ]
T2926 5609-5612 CC denotes and
T2927 5613-5615 PRP denotes we
T2928 5616-5627 RB denotes accordingly
T2929 5628-5636 VBD denotes assessed
T2930 5637-5644 IN denotes whether
T2931 5645-5653 NNP denotes PKD-null
T2932 5654-5658 NNP denotes DT40
T2933 5659-5664 NNS denotes cells
T2934 5665-5669 VBP denotes have
T2935 5670-5679 JJ denotes defective
T2936 5680-5695 NN denotes phosphorylation
T2937 5696-5698 IN denotes of
T2938 5699-5704 NNP denotes HSP27
T2939 5705-5707 IN denotes on
T2940 5708-5714 NN denotes serine
T2941 5715-5717 CD denotes 82
T2942 5717-5718 , denotes ,
T2943 5719-5722 DT denotes the
T2944 5723-5731 VBN denotes proposed
T2945 5732-5736 NNP denotes PKD1
T2946 5737-5746 VB denotes substrate
T2947 5747-5755 NN denotes sequence
T2948 5755-5756 . denotes .
T2949 5757-5759 PRP denotes We
T2950 5760-5769 RB denotes initially
T2951 5770-5782 VBD denotes investigated
T2952 5783-5786 DT denotes the
T2953 5787-5797 NN denotes regulation
T2954 5798-5800 IN denotes of
T2955 5801-5806 NNP denotes HSP27
T2956 5807-5822 NN denotes phosphorylation
T2957 5823-5825 IN denotes in
T2958 5826-5832 JJ denotes single
T2959 5833-5841 NN denotes knockout
T2960 5842-5846 NNP denotes DT40
T2961 5847-5848 NNP denotes B
T2962 5849-5854 NNS denotes cells
T2963 5855-5862 VBG denotes lacking
T2964 5863-5869 CC denotes either
T2965 5870-5874 CD denotes PKD1
T2966 5875-5877 CC denotes or
T2967 5878-5882 CD denotes PKD3
T2968 5882-5883 . denotes .
T2969 5884-5886 IN denotes As
T2970 5887-5892 VBN denotes shown
T2971 5893-5895 IN denotes in
T2972 5896-5900 NNP denotes Fig.
T2973 5901-5903 NNP denotes 1B
T2974 5903-5904 , denotes ,
T2975 5905-5915 NN denotes activation
T2976 5916-5918 IN denotes of
T2977 5919-5922 DT denotes the
T2978 5923-5926 NNP denotes BCR
T2979 5927-5929 CC denotes or
T2980 5930-5939 NN denotes treatment
T2981 5940-5944 IN denotes with
T2982 5945-5948 DT denotes the
T2983 5949-5960 JJ denotes DAG-mimetic
T2984 5961-5965 NNP denotes PdBu
T2985 5966-5975 VBD denotes increased
T2986 5976-5979 DT denotes the
T2987 5980-5986 NNS denotes levels
T2988 5987-5989 IN denotes of
T2989 5990-5995 NNP denotes HSP27
T2990 5996-6011 NN denotes phosphorylation
T2991 6012-6014 IN denotes at
T2992 6015-6018 CD denotes S82
T2993 6019-6021 IN denotes in
T2994 6022-6031 JJ denotes wild-type
T2995 6032-6036 NNP denotes DT40
T2996 6037-6038 NNP denotes B
T2997 6039-6044 NNS denotes cells
T2998 6044-6045 . denotes .
T2999 6046-6049 NNP denotes BCR
T3000 6050-6053 CC denotes and
T3001 6054-6061 JJ denotes phorbol
T3002 6062-6067 NN denotes ester
T3003 6068-6075 NNS denotes signals
T3004 6076-6080 VBD denotes were
T3005 6081-6085 RB denotes also
T3006 6086-6090 JJ denotes able
T3007 6091-6093 TO denotes to
T3008 6094-6102 VB denotes increase
T3009 6103-6108 NNP denotes HSP27
T3010 6109-6124 NN denotes phosphorylation
T3011 6125-6127 IN denotes in
T3012 6128-6132 CD denotes PKD1
T3013 6133-6135 CC denotes or
T3014 6136-6140 CD denotes PKD3
T3015 6141-6147 JJ denotes single
T3016 6148-6156 NN denotes knockout
T3017 6157-6161 NNP denotes DT40
T3018 6162-6163 NNP denotes B
T3019 6164-6169 NNS denotes cells
T3020 6170-6171 -LRB- denotes (
T3021 6171-6175 NNP denotes Fig.
T3022 6176-6178 NNP denotes 1B
T3023 6178-6179 -RRB- denotes )
T3024 6179-6180 . denotes .
T3025 6181-6188 RB denotes However
T3026 6188-6189 , denotes ,
T3027 6190-6193 NNP denotes BCR
T3028 6193-6194 : denotes -
T3029 6195-6198 CC denotes and
T3030 6199-6206 VB denotes phorbol
T3031 6207-6220 JJ denotes ester-induced
T3032 6221-6236 NN denotes phosphorylation
T3033 6237-6239 IN denotes of
T3034 6240-6245 NNP denotes HSP27
T3035 6246-6248 IN denotes on
T3036 6249-6252 NNP denotes S82
T3037 6253-6256 VBD denotes was
T3038 6257-6266 VBN denotes abolished
T3039 6267-6269 IN denotes in
T3040 6270-6271 NNP denotes B
T3041 6272-6277 NNS denotes cells
T3042 6278-6282 WDT denotes that
T3043 6283-6289 VBD denotes lacked
T3044 6290-6294 DT denotes both
T3045 6295-6299 NNP denotes PKD1
T3046 6300-6303 CC denotes and
T3047 6304-6308 NNP denotes PKD3
T3048 6309-6310 -LRB- denotes (
T3049 6310-6314 NNP denotes Fig.
T3050 6315-6317 NNP denotes 1C
T3051 6317-6318 -RRB- denotes )
T3052 6318-6319 . denotes .
T3053 6320-6333 RB denotes Significantly
T3054 6333-6334 , denotes ,
T3055 6335-6354 JJ denotes doxycycline-induced
T3056 6355-6365 NN denotes expression
T3057 6366-6368 IN denotes of
T3058 6369-6372 DT denotes the
T3059 6373-6382 NN denotes Flag-PKD3
T3060 6383-6392 NN denotes transgene
T3061 6393-6395 IN denotes in
T3062 6396-6399 DT denotes the
T3063 6400-6406 JJ denotes double
T3064 6407-6415 NN denotes knockout
T3065 6416-6421 NNS denotes cells
T3066 6422-6425 VBD denotes was
T3067 6426-6436 JJ denotes sufficient
T3068 6437-6439 TO denotes to
T3069 6440-6447 VB denotes restore
T3070 6448-6454 JJ denotes normal
T3071 6455-6465 NN denotes regulation
T3072 6466-6468 IN denotes of
T3073 6469-6474 NNP denotes HSP27
T3074 6475-6490 NN denotes phosphorylation
T3075 6491-6492 -LRB- denotes (
T3076 6492-6496 NNP denotes Fig.
T3077 6497-6499 NNP denotes 1C
T3078 6499-6500 -RRB- denotes )
T3079 6500-6501 . denotes .
T3080 6502-6504 IN denotes In
T3081 6505-6513 NN denotes contrast
T3082 6513-6514 , denotes ,
T3083 6515-6525 NN denotes expression
T3084 6526-6528 IN denotes of
T3085 6529-6530 DT denotes a
T3086 6531-6547 JJ denotes kinase-deficient
T3087 6548-6552 NN denotes PKD3
T3088 6553-6559 JJ denotes mutant
T3089 6560-6567 NN denotes protein
T3090 6568-6570 IN denotes in
T3091 6571-6574 DT denotes the
T3092 6575-6581 JJ denotes double
T3093 6582-6590 NN denotes knockout
T3094 6591-6596 NNS denotes cells
T3095 6597-6600 VBD denotes was
T3096 6601-6604 RB denotes not
T3097 6605-6609 JJ denotes able
T3098 6610-6612 TO denotes to
T3099 6613-6620 VB denotes restore
T3100 6621-6624 NNP denotes BCR
T3101 6624-6625 : denotes -
T3102 6626-6628 CC denotes or
T3103 6629-6636 VB denotes phorbol
T3104 6637-6650 JJ denotes ester-induced
T3105 6651-6656 NNP denotes HSP27
T3106 6657-6672 NN denotes phosphorylation
T3107 6673-6674 -LRB- denotes (
T3108 6674-6678 NNP denotes Fig.
T3109 6679-6681 NNP denotes 1D
T3110 6681-6682 -RRB- denotes )
T3111 6682-6683 . denotes .
T3112 6684-6689 RB denotes Hence
T3113 6689-6690 , denotes ,
T3114 6691-6695 NNP denotes PKD3
T3115 6696-6698 RB denotes as
T3116 6699-6703 RB denotes well
T3117 6704-6706 IN denotes as
T3118 6707-6711 NNP denotes PKD1
T3119 6712-6715 MD denotes can
T3120 6716-6724 VB denotes regulate
T3121 6725-6730 NNP denotes HSP27
T3122 6731-6746 NN denotes phosphorylation
T3123 6747-6750 CC denotes and
T3124 6751-6753 IN denotes in
T3125 6754-6758 NNP denotes DT40
T3126 6759-6760 NNP denotes B
T3127 6761-6766 NNS denotes cells
T3128 6767-6771 PRP denotes they
T3129 6772-6775 VBP denotes are
T3130 6776-6788 RB denotes functionally
T3131 6789-6798 JJ denotes redundant
T3132 6799-6801 IN denotes as
T3133 6802-6807 NNP denotes HSP27
T3134 6808-6815 NNS denotes kinases
T3135 6815-6816 . denotes .
T4218 6823-6831 NNP denotes Cellular
T4219 6832-6845 NN denotes proliferation
T4220 6846-6849 CC denotes and
T4221 6850-6858 NN denotes survival
T4222 6859-6861 IN denotes in
T4223 6862-6866 NNP denotes DT40
T4224 6867-6868 NNP denotes B
T4225 6869-6874 NNS denotes cells
T4226 6875-6882 VBG denotes lacking
T4227 6883-6893 NN denotes expression
T4228 6894-6896 IN denotes of
T4229 6897-6900 NNP denotes PKD
T4230 6901-6907 NN denotes family
T4231 6908-6915 VBZ denotes kinases
T4232 6916-6919 NNP denotes PKD
T4233 6920-6927 NNS denotes enzymes
T4234 6928-6932 VBP denotes have
T4235 6933-6943 RB denotes previously
T4236 6944-6948 VBN denotes been
T4237 6949-6955 VBN denotes linked
T4238 6956-6958 TO denotes to
T4239 6959-6962 DT denotes the
T4240 6963-6973 NN denotes regulation
T4241 6974-6976 IN denotes of
T4242 6977-6981 NN denotes cell
T4243 6982-6995 NN denotes proliferation
T4244 6996-6999 CC denotes and
T4245 7000-7008 NN denotes survival
T4246 7009-7010 -LRB- denotes (
T4247 7010-7018 VBN denotes reviewed
T4248 7019-7021 IN denotes in
T4249 7022-7023 NNP denotes [
T4250 7023-7025 CD denotes 20
T4251 7025-7026 NNP denotes ]
T4252 7026-7027 -RRB- denotes )
T4253 7027-7028 . denotes .
T4254 7029-7031 TO denotes To
T4255 7032-7043 VB denotes investigate
T4256 7044-7047 DT denotes the
T4257 7048-7054 NN denotes effect
T4258 7055-7059 WDT denotes that
T4259 7060-7064 NN denotes loss
T4260 7065-7067 IN denotes of
T4261 7068-7071 NNP denotes PKD
T4262 7072-7079 NNS denotes kinases
T4263 7080-7083 VBD denotes had
T4264 7084-7086 IN denotes on
T4265 7087-7088 NNP denotes B
T4266 7089-7093 NN denotes cell
T4267 7094-7102 NN denotes survival
T4268 7103-7109 CC denotes and/or
T4269 7110-7123 NN denotes proliferation
T4270 7124-7126 PRP denotes we
T4271 7127-7135 VBD denotes cultured
T4272 7136-7145 JJ denotes wild-type
T4273 7146-7149 CC denotes and
T4274 7150-7158 JJ denotes PKD-null
T4275 7159-7164 NNS denotes cells
T4276 7165-7167 IN denotes in
T4277 7168-7171 DT denotes the
T4278 7172-7180 NN denotes presence
T4279 7181-7182 -LRB- denotes (
T4280 7182-7188 CD denotes PKD1/3
T4281 7188-7189 CD denotes
T4282 7189-7190 NN denotes /
T4283 7190-7191 NN denotes
T4284 7191-7192 : denotes :
T4285 7193-7202 NN denotes Flag-PKD3
T4286 7202-7203 NN denotes +
T4287 7203-7205 NN denotes ve
T4288 7205-7206 -RRB- denotes )
T4289 7207-7209 CC denotes or
T4290 7210-7217 NN denotes absence
T4291 7218-7219 -LRB- denotes (
T4292 7219-7225 CD denotes PKD1/3
T4293 7225-7226 CD denotes
T4294 7226-7227 NN denotes /
T4295 7227-7228 NN denotes
T4296 7228-7229 -RRB- denotes )
T4297 7230-7232 IN denotes of
T4298 7233-7244 NN denotes doxycycline
T4299 7245-7248 CC denotes and
T4300 7249-7258 VBD denotes monitored
T4301 7259-7270 JJ denotes exponential
T4302 7271-7277 NN denotes growth
T4303 7277-7278 . denotes .
T4304 7279-7281 IN denotes As
T4305 7282-7287 VBN denotes shown
T4306 7288-7290 IN denotes in
T4307 7291-7295 NNP denotes Fig.
T4308 7296-7298 NNP denotes 2A
T4309 7298-7299 , denotes ,
T4310 7300-7306 NNP denotes PKD1/3
T4311 7306-7307 VBD denotes
T4312 7307-7308 CD denotes /
T4313 7308-7309 NN denotes
T4314 7310-7315 NNS denotes cells
T4315 7316-7328 VBD denotes proliferated
T4316 7329-7342 RB denotes exponentially
T4317 7343-7346 CC denotes and
T4318 7347-7360 NN denotes re-expression
T4319 7361-7363 IN denotes of
T4320 7364-7373 NN denotes Flag-PKD3
T4321 7374-7376 IN denotes in
T4322 7377-7382 DT denotes these
T4323 7383-7388 NNS denotes cells
T4324 7389-7392 VBD denotes had
T4325 7393-7395 DT denotes no
T4326 7396-7402 NN denotes impact
T4327 7403-7405 IN denotes on
T4328 7406-7409 DT denotes the
T4329 7410-7414 NN denotes rate
T4330 7415-7417 IN denotes of
T4331 7418-7431 NN denotes proliferation
T4332 7431-7432 . denotes .
T4333 7433-7444 RB denotes Furthermore
T4334 7444-7445 , denotes ,
T4335 7446-7449 DT denotes the
T4336 7450-7459 NN denotes viability
T4337 7460-7462 IN denotes of
T4338 7463-7469 CD denotes PKD1/3
T4339 7469-7470 CD denotes
T4340 7470-7471 NN denotes /
T4341 7471-7472 NN denotes
T4342 7473-7474 NNP denotes B
T4343 7475-7480 NNS denotes cells
T4344 7481-7487 IN denotes during
T4345 7488-7495 JJ denotes routine
T4346 7496-7505 NN denotes culturing
T4347 7506-7509 VBD denotes was
T4348 7510-7513 RB denotes not
T4349 7514-7527 RB denotes significantly
T4350 7528-7537 JJ denotes different
T4351 7538-7542 IN denotes from
T4352 7543-7547 DT denotes that
T4353 7548-7550 IN denotes of
T4354 7551-7560 JJ denotes wild-type
T4355 7561-7562 NNP denotes B
T4356 7563-7568 NNS denotes cells
T4357 7569-7570 -LRB- denotes (
T4358 7570-7574 NNS denotes data
T4359 7575-7578 RB denotes not
T4360 7579-7584 VBN denotes shown
T4361 7584-7585 -RRB- denotes )
T4362 7585-7586 . denotes .
T4363 7587-7589 PRP denotes It
T4364 7590-7593 VBD denotes was
T4365 7594-7599 VBN denotes noted
T4366 7600-7604 IN denotes that
T4367 7605-7608 DT denotes the
T4368 7609-7619 NN denotes population
T4369 7620-7628 VBG denotes doubling
T4370 7629-7633 NN denotes time
T4371 7634-7636 IN denotes of
T4372 7637-7643 CD denotes PKD1/3
T4373 7643-7644 CD denotes
T4374 7644-7645 NN denotes /
T4375 7645-7646 NN denotes
T4376 7647-7652 NNS denotes cells
T4377 7653-7656 VBD denotes was
T4378 7657-7665 RB denotes slightly
T4379 7666-7672 JJR denotes slower
T4380 7673-7677 IN denotes than
T4381 7678-7682 DT denotes that
T4382 7683-7685 IN denotes of
T4383 7686-7690 JJ denotes wild
T4384 7691-7695 NN denotes type
T4385 7696-7700 CD denotes DT40
T4386 7701-7706 NNS denotes cells
T4387 7707-7708 -LRB- denotes (
T4388 7708-7712 CD denotes 12.7
T4389 7713-7714 CD denotes ±
T4390 7715-7718 CD denotes 2.8
T4391 7719-7720 NN denotes h
T4392 7721-7727 IN denotes versus
T4393 7728-7732 CD denotes 10.2
T4394 7733-7734 CD denotes ±
T4395 7735-7738 CD denotes 0.4
T4396 7739-7740 NN denotes h
T4397 7740-7741 -RRB- denotes )
T4398 7742-7745 CC denotes but
T4399 7746-7749 DT denotes the
T4400 7750-7757 NN denotes failure
T4401 7758-7760 IN denotes of
T4402 7761-7765 CD denotes PKD3
T4403 7766-7779 NN denotes re-expression
T4404 7780-7782 TO denotes to
T4405 7783-7789 VB denotes modify
T4406 7790-7793 DT denotes the
T4407 7794-7807 NN denotes proliferation
T4408 7808-7812 NN denotes rate
T4409 7813-7815 IN denotes of
T4410 7816-7822 CD denotes PKD1/3
T4411 7822-7823 CD denotes
T4412 7823-7824 NN denotes /
T4413 7824-7825 NN denotes
T4414 7826-7831 NNS denotes cells
T4415 7832-7840 VBZ denotes suggests
T4416 7841-7845 IN denotes that
T4417 7846-7851 DT denotes these
T4418 7852-7857 JJ denotes small
T4419 7858-7869 NNS denotes differences
T4420 7870-7874 VBD denotes were
T4421 7875-7879 RBS denotes most
T4422 7880-7886 JJ denotes likely
T4423 7887-7890 DT denotes the
T4424 7891-7897 NN denotes result
T4425 7898-7900 IN denotes of
T4426 7901-7907 JJ denotes clonal
T4427 7908-7917 NN denotes variation
T4428 7918-7921 CC denotes and
T4429 7922-7926 VBD denotes were
T4430 7927-7930 RB denotes not
T4431 7931-7937 VBN denotes caused
T4432 7938-7950 RB denotes specifically
T4433 7951-7953 IN denotes by
T4434 7954-7958 NN denotes loss
T4435 7959-7961 IN denotes of
T4436 7962-7965 NNP denotes PKD
T4437 7966-7973 VBZ denotes enzymes
T4438 7973-7974 . denotes .
T4439 7975-7979 RB denotes Thus
T4440 7979-7980 , denotes ,
T4441 7981-7984 NNP denotes PKD
T4442 7985-7991 NN denotes family
T4443 7992-7999 NNS denotes enzymes
T4444 8000-8003 VBP denotes are
T4445 8004-8007 RB denotes not
T4446 8008-8017 JJ denotes essential
T4447 8018-8021 IN denotes for
T4448 8022-8032 VBG denotes regulating
T4449 8033-8038 JJ denotes basal
T4450 8039-8047 NN denotes survival
T4451 8048-8051 CC denotes and
T4452 8052-8065 NN denotes proliferation
T4453 8066-8068 IN denotes of
T4454 8069-8073 NNP denotes DT40
T4455 8074-8075 NNP denotes B
T4456 8076-8081 NNS denotes cells
T4457 8081-8082 . denotes .
T4458 8083-8086 NNP denotes PKD
T4459 8087-8094 VBZ denotes enzymes
T4460 8094-8095 , denotes ,
T4461 8096-8108 RB denotes specifically
T4462 8109-8113 CD denotes PKD1
T4463 8114-8117 CC denotes and
T4464 8118-8122 NNP denotes PKD2
T4465 8122-8123 , denotes ,
T4466 8124-8128 VBP denotes have
T4467 8129-8139 RB denotes previously
T4468 8140-8144 VBN denotes been
T4469 8145-8151 VBN denotes linked
T4470 8152-8154 TO denotes to
T4471 8155-8156 DT denotes a
T4472 8157-8167 JJ denotes protective
T4473 8168-8172 NN denotes role
T4474 8173-8180 IN denotes against
T4475 8181-8190 JJ denotes oxidative
T4476 8191-8205 JJ denotes stress-induced
T4477 8206-8212 NN denotes injury
T4478 8213-8215 IN denotes in
T4479 8216-8219 NNP denotes 3T3
T4480 8220-8230 NN denotes fibroblast
T4481 8230-8231 , denotes ,
T4482 8232-8236 NNP denotes HeLa
T4483 8237-8240 CC denotes and
T4484 8241-8251 JJ denotes epithelial
T4485 8252-8256 NN denotes cell
T4486 8257-8262 NNS denotes lines
T4487 8263-8264 NNP denotes [
T4488 8264-8269 CD denotes 17,30
T4489 8270-8272 CD denotes 32
T4490 8272-8273 NN denotes ]
T4491 8273-8274 . denotes .
T4492 8275-8277 PRP denotes We
T4493 8278-8287 RB denotes therefore
T4494 8288-8297 VBD denotes addressed
T4495 8298-8301 DT denotes the
T4496 8302-8306 NN denotes role
T4497 8307-8309 IN denotes of
T4498 8310-8313 NNP denotes PKD
T4499 8314-8320 NN denotes family
T4500 8321-8328 NNS denotes kinases
T4501 8329-8331 IN denotes in
T4502 8332-8342 VBG denotes regulating
T4503 8343-8344 NNP denotes B
T4504 8345-8349 NN denotes cell
T4505 8350-8358 NN denotes survival
T4506 8359-8361 IN denotes in
T4507 8362-8370 NN denotes response
T4508 8371-8373 TO denotes to
T4509 8374-8383 JJ denotes oxidative
T4510 8384-8390 NN denotes stress
T4511 8391-8394 CC denotes and
T4512 8395-8400 JJ denotes other
T4513 8401-8407 NN denotes stress
T4514 8408-8415 NNS denotes stimuli
T4515 8415-8416 . denotes .
T4516 8417-8419 IN denotes As
T4517 8420-8425 VBN denotes shown
T4518 8426-8428 IN denotes in
T4519 8429-8433 NNP denotes Fig.
T4520 8434-8436 NNP denotes 2B
T4521 8436-8437 , denotes ,
T4522 8438-8442 NN denotes loss
T4523 8443-8445 IN denotes of
T4524 8446-8452 CD denotes PKD1/3
T4525 8453-8463 NN denotes expression
T4526 8464-8467 VBD denotes had
T4527 8468-8470 DT denotes no
T4528 8471-8482 JJ denotes significant
T4529 8483-8489 NN denotes impact
T4530 8490-8492 IN denotes on
T4531 8493-8496 DT denotes the
T4532 8497-8505 NN denotes survival
T4533 8506-8508 IN denotes of
T4534 8509-8513 NNP denotes DT40
T4535 8514-8515 NNP denotes B
T4536 8516-8521 NNS denotes cells
T4537 8522-8524 IN denotes in
T4538 8525-8533 NN denotes response
T4539 8534-8536 TO denotes to
T4540 8537-8550 JJ denotes mitochondrial
T4541 8551-8557 NN denotes stress
T4542 8558-8565 NNS denotes stimuli
T4543 8566-8567 -LRB- denotes (
T4544 8567-8571 CD denotes H2O2
T4545 8572-8574 CC denotes or
T4546 8575-8580 NN denotes serum
T4547 8581-8592 NN denotes deprivation
T4548 8592-8593 -RRB- denotes )
T4549 8593-8594 : denotes ;
T4550 8595-8598 NNP denotes DNA
T4551 8599-8607 VBG denotes damaging
T4552 8608-8614 NNS denotes agents
T4553 8615-8616 -LRB- denotes (
T4554 8616-8625 NN denotes etoposide
T4555 8626-8628 CC denotes or
T4556 8629-8640 NN denotes doxorubicin
T4557 8640-8641 -RRB- denotes )
T4558 8641-8642 : denotes ;
T4559 8643-8645 NNP denotes ER
T4560 8646-8653 NN denotes pathway
T4561 8654-8660 NN denotes stress
T4562 8661-8664 JJ denotes due
T4563 8665-8667 TO denotes to
T4564 8668-8675 NN denotes calcium
T4565 8676-8684 NN denotes overload
T4566 8685-8686 -LRB- denotes (
T4567 8686-8698 NN denotes thapsigargin
T4568 8698-8699 -RRB- denotes )
T4569 8700-8702 CC denotes or
T4570 8703-8712 VBG denotes following
T4571 8713-8722 JJ denotes prolonged
T4572 8723-8732 NN denotes treatment
T4573 8733-8737 IN denotes with
T4574 8738-8745 NN denotes phorbol
T4575 8746-8752 NNS denotes esters
T4576 8753-8755 CC denotes or
T4577 8756-8768 NNP denotes Trichostatin
T4578 8769-8770 NNP denotes A
T4579 8770-8771 , denotes ,
T4580 8772-8774 DT denotes an
T4581 8775-8784 NN denotes inhibitor
T4582 8785-8787 IN denotes of
T4583 8788-8793 NN denotes class
T4584 8794-8798 NNP denotes I/II
T4585 8799-8804 NNP denotes HDACs
T4586 8804-8805 . denotes .
T4587 8806-8810 RB denotes Thus
T4588 8810-8811 , denotes ,
T4589 8812-8815 NNP denotes PKD
T4590 8816-8823 NNS denotes kinases
T4591 8824-8826 VBP denotes do
T4592 8827-8830 RB denotes not
T4593 8831-8835 VB denotes play
T4594 8836-8838 DT denotes an
T4595 8839-8848 JJ denotes essential
T4596 8849-8853 NN denotes role
T4597 8854-8856 IN denotes in
T4598 8857-8867 VBG denotes regulating
T4599 8868-8869 NNP denotes B
T4600 8870-8874 NN denotes cell
T4601 8875-8883 NN denotes survival
T4602 8884-8886 IN denotes in
T4603 8887-8895 NN denotes response
T4604 8896-8898 TO denotes to
T4605 8899-8900 DT denotes a
T4606 8901-8906 NN denotes range
T4607 8907-8909 IN denotes of
T4608 8910-8919 JJ denotes different
T4609 8920-8926 NN denotes stress
T4610 8927-8934 NNS denotes stimuli
T4611 8934-8935 . denotes .
T5769 8942-8949 NN denotes Antigen
T5770 8950-8958 NN denotes receptor
T5771 8959-8968 VBN denotes regulated
T5772 8969-8979 JJ denotes signalling
T5773 8980-8988 NNS denotes pathways
T5774 8989-8991 IN denotes in
T5775 8992-9000 NNP denotes PKD-null
T5776 9001-9005 NNP denotes DT40
T5777 9006-9007 NNP denotes B
T5778 9008-9013 NNS denotes cells
T5779 9014-9016 TO denotes To
T5780 9017-9024 RBR denotes further
T5781 9025-9032 VB denotes explore
T5782 9033-9036 DT denotes the
T5783 9037-9049 NN denotes contribution
T5784 9050-9052 IN denotes of
T5785 9053-9056 NNP denotes PKD
T5786 9057-9064 VBZ denotes kinases
T5787 9065-9067 TO denotes to
T5788 9068-9072 NNP denotes DT40
T5789 9073-9074 NNP denotes B
T5790 9075-9079 NN denotes cell
T5791 9080-9087 NN denotes biology
T5792 9088-9090 PRP denotes we
T5793 9091-9103 VBD denotes investigated
T5794 9104-9111 IN denotes whether
T5795 9112-9120 JJ denotes specific
T5796 9121-9134 JJ denotes BCR-regulated
T5797 9135-9145 JJ denotes signalling
T5798 9146-9152 NNS denotes events
T5799 9153-9157 VBD denotes were
T5800 9158-9167 JJ denotes defective
T5801 9168-9170 IN denotes in
T5802 9171-9174 DT denotes the
T5803 9175-9183 NNP denotes PKD-null
T5804 9184-9185 NNP denotes B
T5805 9186-9191 NNS denotes cells
T5806 9191-9192 . denotes .
T5807 9193-9200 JJ denotes Initial
T5808 9201-9212 NNS denotes experiments
T5809 9213-9221 VBD denotes revealed
T5810 9222-9226 IN denotes that
T5811 9227-9234 NN denotes surface
T5812 9235-9245 NN denotes expression
T5813 9246-9248 IN denotes of
T5814 9249-9252 DT denotes the
T5815 9253-9256 NNP denotes BCR
T5816 9257-9260 VBD denotes was
T5817 9261-9268 VBN denotes reduced
T5818 9269-9271 IN denotes in
T5819 9272-9278 CD denotes PKD1/3
T5820 9278-9279 CD denotes
T5821 9279-9280 NN denotes /
T5822 9280-9281 NN denotes
T5823 9282-9283 -LRB- denotes (
T5824 9283-9286 CC denotes and
T5825 9287-9289 IN denotes in
T5826 9290-9296 CD denotes PKD1/3
T5827 9296-9297 CD denotes
T5828 9297-9298 NN denotes /
T5829 9298-9299 NN denotes
T5830 9299-9300 : denotes :
T5831 9300-9309 NN denotes Flag-PKD3
T5832 9309-9310 NN denotes +
T5833 9310-9312 NN denotes ve
T5834 9312-9313 -RRB- denotes )
T5835 9314-9319 NNS denotes cells
T5836 9320-9328 VBN denotes compared
T5837 9329-9331 TO denotes to
T5838 9332-9341 JJ denotes wild-type
T5839 9342-9346 NNP denotes DT40
T5840 9347-9348 NNP denotes B
T5841 9349-9354 NNS denotes cells
T5842 9355-9356 -LRB- denotes (
T5843 9356-9360 NNP denotes Fig.
T5844 9361-9363 NNP denotes 3A
T5845 9364-9367 CC denotes and
T5846 9368-9372 NNS denotes data
T5847 9373-9376 RB denotes not
T5848 9377-9382 VBN denotes shown
T5849 9382-9383 -RRB- denotes )
T5850 9383-9384 . denotes .
T5851 9385-9397 RB denotes Nevertheless
T5852 9397-9398 , denotes ,
T5853 9399-9415 JJ denotes BCR-crosslinking
T5854 9416-9418 IN denotes of
T5855 9419-9425 CD denotes PKD1/3
T5856 9425-9426 CD denotes
T5857 9426-9427 NN denotes /
T5858 9427-9428 NN denotes
T5859 9429-9434 NNS denotes cells
T5860 9435-9438 VBD denotes was
T5861 9439-9449 JJ denotes sufficient
T5862 9450-9452 TO denotes to
T5863 9453-9459 VB denotes induce
T5864 9460-9463 DT denotes the
T5865 9464-9474 NN denotes activation
T5866 9475-9477 IN denotes of
T5867 9478-9479 DT denotes a
T5868 9480-9486 NN denotes number
T5869 9487-9489 IN denotes of
T5870 9490-9500 VBG denotes signalling
T5871 9501-9509 NNS denotes cascades
T5872 9509-9510 , denotes ,
T5873 9511-9518 JJ denotes similar
T5874 9519-9521 TO denotes to
T5875 9522-9526 DT denotes that
T5876 9527-9535 VBN denotes observed
T5877 9536-9538 IN denotes in
T5878 9539-9548 JJ denotes wild-type
T5879 9549-9554 NNS denotes cells
T5880 9555-9556 -LRB- denotes (
T5881 9556-9560 NNP denotes Fig.
T5882 9561-9563 NNP denotes 3B
T5883 9563-9564 -RRB- denotes )
T5884 9564-9565 . denotes .
T5885 9566-9571 RB denotes Hence
T5886 9571-9572 , denotes ,
T5887 9573-9584 JJ denotes BCR-induced
T5888 9585-9595 NN denotes activation
T5889 9596-9598 IN denotes of
T5890 9599-9602 DT denotes the
T5891 9603-9606 NNP denotes Akt
T5892 9606-9607 , denotes ,
T5893 9608-9616 NNP denotes mTOR/p70
T5894 9617-9619 NNP denotes S6
T5895 9620-9626 NN denotes kinase
T5896 9627-9628 -LRB- denotes (
T5897 9628-9630 IN denotes as
T5898 9631-9636 VBN denotes shown
T5899 9637-9639 IN denotes by
T5900 9640-9642 CD denotes S6
T5901 9643-9652 JJ denotes ribosomal
T5902 9653-9660 NN denotes protein
T5903 9661-9676 NN denotes phosphorylation
T5904 9676-9677 -RRB- denotes )
T5905 9678-9681 CC denotes and
T5906 9682-9686 NNP denotes MAPK
T5907 9687-9697 VBG denotes signalling
T5908 9698-9706 NNS denotes pathways
T5909 9707-9710 VBD denotes was
T5910 9711-9718 RB denotes clearly
T5911 9719-9729 JJ denotes detectable
T5912 9730-9732 IN denotes in
T5913 9733-9744 NNP denotes PKD1/3-null
T5914 9745-9746 NNP denotes B
T5915 9747-9752 NNS denotes cells
T5916 9753-9754 -LRB- denotes (
T5917 9754-9758 NNP denotes Fig.
T5918 9759-9761 NNP denotes 3B
T5919 9761-9762 -RRB- denotes )
T5920 9762-9763 . denotes .
T5921 9764-9775 RB denotes Furthermore
T5922 9775-9776 , denotes ,
T5923 9777-9785 JJ denotes enhanced
T5924 9786-9794 NN denotes tyrosine
T5925 9795-9810 NN denotes phosphorylation
T5926 9811-9813 IN denotes of
T5927 9814-9822 JJ denotes multiple
T5928 9823-9831 JJ denotes cellular
T5929 9832-9840 NNS denotes proteins
T5930 9841-9843 RB denotes as
T5931 9844-9848 RB denotes well
T5932 9849-9851 IN denotes as
T5933 9852-9854 DT denotes an
T5934 9855-9863 NN denotes increase
T5935 9864-9866 IN denotes in
T5936 9867-9880 JJ denotes intracellular
T5937 9881-9888 NN denotes calcium
T5938 9889-9895 NNS denotes levels
T5939 9896-9899 VBD denotes was
T5940 9900-9904 RB denotes also
T5941 9905-9913 VBN denotes observed
T5942 9914-9923 VBG denotes following
T5943 9924-9927 NNP denotes BCR
T5944 9928-9939 NN denotes stimulation
T5945 9940-9942 IN denotes of
T5946 9943-9954 NNP denotes PKD1/3-null
T5947 9955-9956 NNP denotes B
T5948 9957-9962 NNS denotes cells
T5949 9963-9964 -LRB- denotes (
T5950 9964-9968 NNS denotes data
T5951 9969-9972 RB denotes not
T5952 9973-9978 VBN denotes shown
T5953 9978-9979 -RRB- denotes )
T5954 9979-9980 . denotes .
T5955 9981-9983 PRP denotes We
T5956 9984-9987 VBD denotes did
T5957 9988-9995 VB denotes observe
T5958 9996-10000 IN denotes that
T5959 10001-10004 DT denotes the
T5960 10005-10013 NN denotes strength
T5961 10014-10016 IN denotes of
T5962 10017-10020 NNP denotes BCR
T5963 10021-10022 -LRB- denotes (
T5964 10022-10025 CC denotes but
T5965 10026-10029 RB denotes not
T5966 10030-10037 VB denotes phorbol
T5967 10038-10043 NN denotes ester
T5968 10043-10044 -RRB- denotes )
T5969 10044-10045 : denotes -
T5970 10045-10052 VBD denotes induced
T5971 10053-10063 NN denotes regulation
T5972 10064-10066 IN denotes of
T5973 10067-10070 DT denotes the
T5974 10071-10080 JJ denotes Erk1-RSK1
T5975 10081-10091 NN denotes signalling
T5976 10092-10099 NN denotes pathway
T5977 10100-10103 VBD denotes was
T5978 10104-10111 VBN denotes reduced
T5979 10112-10114 IN denotes in
T5980 10115-10121 CD denotes PKD1/3
T5981 10121-10122 CD denotes
T5982 10122-10123 NN denotes /
T5983 10123-10124 NN denotes
T5984 10125-10126 NNP denotes B
T5985 10127-10132 NNS denotes cells
T5986 10133-10141 VBN denotes compared
T5987 10142-10144 TO denotes to
T5988 10145-10154 JJ denotes wild-type
T5989 10155-10156 NNP denotes B
T5990 10157-10162 NNS denotes cells
T5991 10163-10164 -LRB- denotes (
T5992 10164-10168 NNP denotes Fig.
T5993 10169-10171 NNP denotes 3B
T5994 10171-10172 -RRB- denotes )
T5995 10172-10173 . denotes .
T5996 10174-10177 CD denotes One
T5997 10178-10192 NN denotes interpretation
T5998 10193-10195 IN denotes of
T5999 10196-10200 DT denotes this
T6000 10201-10205 NN denotes data
T6001 10206-10208 VBZ denotes is
T6002 10209-10213 IN denotes that
T6003 10214-10217 NNP denotes PKD
T6004 10218-10225 VBZ denotes enzymes
T6005 10226-10229 MD denotes may
T6006 10230-10238 VB denotes modulate
T6007 10239-10242 NNP denotes Erk
T6008 10243-10253 NN denotes activation
T6009 10253-10254 . denotes .
T6010 10255-10261 RB denotes Indeed
T6011 10261-10262 , denotes ,
T6012 10263-10266 NNP denotes PKD
T6013 10267-10274 NNS denotes enzymes
T6014 10275-10279 VBP denotes have
T6015 10280-10290 RB denotes previously
T6016 10291-10295 VBN denotes been
T6017 10296-10302 VBN denotes linked
T6018 10303-10305 TO denotes to
T6019 10306-10309 DT denotes the
T6020 10310-10316 NN denotes growth
T6021 10317-10333 JJ denotes factor-regulated
T6022 10334-10337 NNP denotes Erk
T6023 10338-10348 NN denotes signalling
T6024 10349-10351 IN denotes in
T6025 10352-10362 NN denotes fibroblast
T6026 10363-10366 CC denotes and
T6027 10367-10378 JJ denotes endothelial
T6028 10379-10383 NN denotes cell
T6029 10384-10389 NNS denotes lines
T6030 10390-10391 NNP denotes [
T6031 10391-10393 CD denotes 33
T6032 10394-10396 CD denotes 35
T6033 10396-10397 NN denotes ]
T6034 10397-10398 . denotes .
T6035 10399-10406 RB denotes However
T6036 10406-10407 , denotes ,
T6037 10408-10419 JJ denotes BCR-induced
T6038 10420-10423 NNP denotes Erk
T6039 10424-10439 NN denotes phosphorylation
T6040 10440-10443 VBD denotes was
T6041 10444-10448 RB denotes also
T6042 10449-10456 VBN denotes reduced
T6043 10457-10459 IN denotes in
T6044 10460-10466 CD denotes PKD1/3
T6045 10466-10467 CD denotes
T6046 10467-10468 NN denotes /
T6047 10468-10469 SYM denotes
T6048 10469-10470 : denotes -
T6049 10470-10479 NN denotes Flag-PKD3
T6050 10479-10480 NN denotes +
T6051 10481-10482 NNP denotes B
T6052 10483-10488 NNS denotes cells
T6053 10489-10490 -LRB- denotes (
T6054 10490-10494 NNS denotes data
T6055 10495-10498 RB denotes not
T6056 10499-10504 VBN denotes shown
T6057 10504-10505 -RRB- denotes )
T6058 10506-10516 VBG denotes suggesting
T6059 10517-10521 IN denotes that
T6060 10522-10529 VBN denotes reduced
T6061 10530-10533 NNP denotes BCR
T6062 10534-10540 NNS denotes levels
T6063 10541-10543 IN denotes on
T6064 10544-10547 DT denotes the
T6065 10548-10555 NN denotes surface
T6066 10556-10558 IN denotes of
T6067 10559-10565 CD denotes PKD1/3
T6068 10565-10566 CD denotes
T6069 10566-10567 NN denotes /
T6070 10567-10568 NN denotes
T6071 10569-10570 -LRB- denotes (
T6072 10570-10573 CC denotes and
T6073 10574-10580 NNP denotes PKD1/3
T6074 10580-10581 VBD denotes
T6075 10581-10582 CD denotes /
T6076 10582-10583 SYM denotes
T6077 10583-10584 : denotes -
T6078 10584-10593 NN denotes Flag-PKD3
T6079 10593-10594 NN denotes +
T6080 10594-10595 -RRB- denotes )
T6081 10596-10597 NNP denotes B
T6082 10598-10603 NNS denotes cells
T6083 10604-10607 MD denotes may
T6084 10608-10614 PRP denotes itself
T6085 10615-10621 VB denotes impact
T6086 10622-10624 IN denotes on
T6087 10625-10628 DT denotes the
T6088 10629-10637 NN denotes strength
T6089 10638-10640 IN denotes of
T6090 10641-10651 NN denotes activation
T6091 10652-10654 IN denotes of
T6092 10655-10659 DT denotes this
T6093 10660-10668 JJ denotes specific
T6094 10669-10682 JJ denotes intracellular
T6095 10683-10693 NN denotes signalling
T6096 10694-10701 NN denotes pathway
T6097 10701-10702 . denotes .
T6098 10703-10705 TO denotes To
T6099 10706-10712 VB denotes search
T6100 10713-10716 IN denotes for
T6101 10717-10722 JJ denotes other
T6102 10723-10732 JJ denotes potential
T6103 10733-10736 NNP denotes PKD
T6104 10737-10744 NNS denotes targets
T6105 10745-10749 WDT denotes that
T6106 10750-10753 MD denotes may
T6107 10754-10758 VB denotes show
T6108 10759-10768 JJ denotes defective
T6109 10769-10779 NN denotes regulation
T6110 10780-10782 IN denotes in
T6111 10783-10789 NNP denotes PKD1/3
T6112 10789-10790 NNP denotes
T6113 10790-10791 NNP denotes /
T6114 10791-10792 NNP denotes
T6115 10793-10797 NNP denotes DT40
T6116 10798-10799 NNP denotes B
T6117 10800-10805 NNS denotes cells
T6118 10805-10806 , denotes ,
T6119 10807-10809 PRP denotes we
T6120 10810-10814 VBD denotes used
T6121 10815-10816 DT denotes a
T6122 10817-10820 NNP denotes PKD
T6123 10821-10830 VB denotes substrate
T6124 10831-10847 JJ denotes phospho-antibody
T6125 10848-10852 IN denotes that
T6126 10853-10863 VBZ denotes recognises
T6127 10864-10873 NN denotes consensus
T6128 10874-10889 NN denotes phosphorylation
T6129 10890-10899 NNS denotes sequences
T6130 10900-10908 VBN denotes targeted
T6131 10909-10911 IN denotes by
T6132 10912-10915 NNP denotes PKD
T6133 10916-10923 VBZ denotes enzymes
T6134 10924-10925 -LRB- denotes (
T6135 10925-10934 NNP denotes LxRxxpS/T
T6136 10934-10935 -RRB- denotes )
T6137 10936-10937 NNP denotes [
T6138 10937-10939 CD denotes 36
T6139 10939-10940 NNP denotes ]
T6140 10940-10941 . denotes .
T6141 10942-10944 IN denotes As
T6142 10945-10950 VBN denotes shown
T6143 10951-10953 IN denotes in
T6144 10954-10958 NNP denotes Fig.
T6145 10959-10961 NNP denotes 3C
T6146 10961-10962 , denotes ,
T6147 10963-10970 NN denotes phorbol
T6148 10971-10976 NN denotes ester
T6149 10976-10977 : denotes -
T6150 10978-10981 CC denotes and
T6151 10982-10993 JJ denotes BCR-induced
T6152 10994-11009 NN denotes phosphorylation
T6153 11010-11012 IN denotes of
T6154 11013-11021 JJ denotes cellular
T6155 11022-11032 NNS denotes substrates
T6156 11033-11041 VBN denotes detected
T6157 11042-11044 IN denotes by
T6158 11045-11049 DT denotes this
T6159 11050-11066 NN denotes phospho-antibody
T6160 11067-11070 VBD denotes was
T6161 11071-11078 JJ denotes similar
T6162 11079-11081 IN denotes in
T6163 11082-11091 JJ denotes wild-type
T6164 11092-11095 CC denotes and
T6165 11096-11102 JJ denotes PKD1/3
T6166 11102-11103 NN denotes
T6167 11103-11104 NN denotes /
T6168 11104-11105 NN denotes
T6169 11106-11111 NNS denotes cells
T6170 11112-11115 CC denotes and
T6171 11116-11118 VBZ denotes is
T6172 11119-11128 RB denotes therefore
T6173 11129-11140 JJ denotes independent
T6174 11141-11143 IN denotes of
T6175 11144-11147 NNP denotes PKD
T6176 11148-11155 VBZ denotes enzymes
T6177 11155-11156 . denotes .
T6178 11157-11164 RB denotes However
T6179 11164-11165 , denotes ,
T6180 11166-11178 NN denotes pretreatment
T6181 11179-11181 IN denotes of
T6182 11182-11186 DT denotes both
T6183 11187-11196 JJ denotes wild-type
T6184 11197-11200 CC denotes and
T6185 11201-11207 JJ denotes PKD1/3
T6186 11207-11208 NN denotes
T6187 11208-11209 NN denotes /
T6188 11209-11210 NN denotes
T6189 11211-11215 NNP denotes DT40
T6190 11216-11217 NNP denotes B
T6191 11218-11223 NNS denotes cells
T6192 11224-11228 IN denotes with
T6193 11229-11238 NNP denotes GF109203X
T6194 11238-11239 , denotes ,
T6195 11240-11241 DT denotes a
T6196 11242-11260 NN denotes bisindoylmaleimide
T6197 11261-11271 NN denotes derivative
T6198 11272-11276 WDT denotes that
T6199 11277-11285 VBZ denotes inhibits
T6200 11286-11290 NNS denotes PKCs
T6201 11291-11300 VBD denotes prevented
T6202 11301-11304 DT denotes the
T6203 11305-11314 NN denotes induction
T6204 11315-11317 IN denotes of
T6205 11318-11326 NNS denotes proteins
T6206 11327-11331 WDT denotes that
T6207 11332-11339 VBP denotes contain
T6208 11340-11354 VBN denotes phosphorylated
T6209 11355-11363 NNP denotes LxRxxS/T
T6210 11364-11370 NNS denotes motifs
T6211 11370-11371 . denotes .
T6212 11372-11376 RB denotes Thus
T6213 11377-11381 NN denotes loss
T6214 11382-11384 IN denotes of
T6215 11385-11391 NNP denotes PKD1/3
T6216 11392-11399 VBZ denotes enzymes
T6217 11400-11404 VBZ denotes does
T6218 11405-11408 RB denotes not
T6219 11409-11417 RB denotes globally
T6220 11418-11425 VB denotes disrupt
T6221 11426-11429 DT denotes the
T6222 11430-11445 NN denotes phosphorylation
T6223 11446-11448 IN denotes of
T6224 11449-11457 JJ denotes cellular
T6225 11458-11466 NNS denotes proteins
T6226 11467-11471 WDT denotes that
T6227 11472-11479 VBP denotes contain
T6228 11480-11489 NNP denotes LxRxxpS/T
T6229 11490-11496 NNS denotes motifs
T6230 11496-11497 . denotes .
T6231 11498-11502 DT denotes This
T6232 11503-11509 NN denotes result
T6233 11510-11512 VBZ denotes is
T6234 11513-11520 RB denotes perhaps
T6235 11521-11524 RB denotes not
T6236 11525-11535 JJ denotes surprising
T6237 11536-11538 IN denotes as
T6238 11539-11547 NNP denotes LxRxxS/T
T6239 11548-11554 NNS denotes motifs
T6240 11555-11559 RB denotes also
T6241 11560-11563 VBP denotes act
T6242 11564-11566 RB denotes as
T6243 11567-11571 JJ denotes good
T6244 11572-11582 NNS denotes substrates
T6245 11583-11586 IN denotes for
T6246 11587-11592 JJ denotes other
T6247 11593-11609 JJ denotes serine/threonine
T6248 11610-11617 NNS denotes kinases
T6249 11618-11622 JJ denotes such
T6250 11623-11625 IN denotes as
T6251 11626-11634 NNP denotes MAPKAPK2
T6252 11634-11635 . denotes .
T6253 11636-11643 RB denotes However
T6254 11644-11649 DT denotes these
T6255 11650-11661 NNS denotes experiments
T6256 11662-11664 VBP denotes do
T6257 11665-11672 VB denotes provide
T6258 11673-11680 JJ denotes further
T6259 11681-11689 NN denotes evidence
T6260 11690-11694 IN denotes that
T6261 11695-11710 JJ denotes phosphospecific
T6262 11711-11719 NN denotes antisera
T6263 11720-11723 VBP denotes are
T6264 11724-11727 RB denotes not
T6265 11728-11740 RB denotes sufficiently
T6266 11741-11750 JJ denotes selective
T6267 11751-11753 TO denotes to
T6268 11754-11756 VB denotes be
T6269 11757-11767 VBN denotes designated
T6270 11768-11774 NN denotes kinase
T6271 11775-11783 JJ denotes specific
T6272 11784-11793 JJ denotes substrate
T6273 11794-11802 NN denotes antisera
T6274 11802-11803 . denotes .
T6275 11804-11815 JJ denotes BCR-induced
T6276 11816-11826 JJ denotes signalling
T6277 11827-11835 NNS denotes pathways
T6278 11836-11845 VBP denotes culminate
T6279 11846-11848 IN denotes in
T6280 11849-11852 DT denotes the
T6281 11853-11863 NN denotes activation
T6282 11864-11866 IN denotes of
T6283 11867-11871 NN denotes gene
T6284 11872-11885 NN denotes transcription
T6285 11886-11892 NNS denotes events
T6286 11893-11897 WDT denotes that
T6287 11898-11905 VBP denotes control
T6288 11906-11907 NNP denotes B
T6289 11908-11912 NN denotes cell
T6290 11913-11921 NN denotes survival
T6291 11921-11922 , denotes ,
T6292 11923-11936 NN denotes proliferation
T6293 11937-11940 CC denotes and
T6294 11941-11949 NN denotes function
T6295 11949-11950 . denotes .
T6296 11951-11953 IN denotes In
T6297 11954-11958 DT denotes this
T6298 11959-11966 NN denotes context
T6299 11966-11967 , denotes ,
T6300 11968-11970 PRP denotes it
T6301 11971-11974 VBZ denotes has
T6302 11975-11979 VBN denotes been
T6303 11980-11988 VBN denotes proposed
T6304 11989-11993 IN denotes that
T6305 11994-11997 NNP denotes PKD
T6306 11998-12004 NN denotes family
T6307 12005-12012 NNS denotes members
T6308 12013-12020 NN denotes control
T6309 12021-12023 IN denotes of
T6310 12024-12028 NN denotes gene
T6311 12029-12042 NN denotes transcription
T6312 12043-12050 IN denotes through
T6313 12051-12061 NN denotes activation
T6314 12062-12064 IN denotes of
T6315 12065-12068 DT denotes the
T6316 12069-12073 NNP denotes NFκB
T6317 12074-12087 NN denotes transcription
T6318 12088-12094 NN denotes factor
T6319 12094-12095 . denotes .
T6320 12096-12100 RB denotes Thus
T6321 12100-12101 , denotes ,
T6322 12102-12114 JJ denotes PKD-mediated
T6323 12115-12125 NN denotes activation
T6324 12126-12128 IN denotes of
T6325 12129-12133 NNP denotes NFκB
T6326 12134-12140 VBZ denotes occurs
T6327 12141-12151 JJ denotes downstream
T6328 12152-12154 IN denotes of
T6329 12155-12156 DT denotes a
T6330 12157-12164 NN denotes variety
T6331 12165-12167 IN denotes of
T6332 12168-12177 JJ denotes different
T6333 12178-12185 NNS denotes signals
T6334 12185-12186 , denotes ,
T6335 12187-12196 VBG denotes including
T6336 12197-12211 JJ denotes mROS/oxidative
T6337 12212-12218 NN denotes stress
T6338 12218-12219 , denotes ,
T6339 12220-12236 JJ denotes lysophosphatidic
T6340 12237-12241 NN denotes acid
T6341 12242-12245 CC denotes and
T6342 12246-12249 DT denotes the
T6343 12250-12257 NNP denotes Bcr-Abl
T6344 12258-12266 NN denotes oncogene
T6345 12267-12268 NNP denotes [
T6346 12268-12282 CD denotes 17,21,23,30,37
T6347 12282-12283 NNP denotes ]
T6348 12283-12284 . denotes .
T6349 12285-12296 RB denotes Furthermore
T6350 12296-12297 , denotes ,
T6351 12298-12308 NN denotes expression
T6352 12309-12311 IN denotes of
T6353 12312-12314 DT denotes an
T6354 12315-12324 VBN denotes activated
T6355 12325-12329 NNP denotes PKD1
T6356 12330-12336 JJ denotes mutant
T6357 12337-12345 VBZ denotes enhances
T6358 12346-12359 JJ denotes HPK1-mediated
T6359 12360-12364 NNP denotes NFκB
T6360 12365-12375 NN denotes activation
T6361 12376-12377 NNP denotes [
T6362 12377-12379 CD denotes 38
T6363 12379-12380 NNP denotes ]
T6364 12380-12381 . denotes .
T6365 12382-12384 IN denotes In
T6366 12385-12386 NNP denotes B
T6367 12387-12392 NNS denotes cells
T6368 12392-12393 , denotes ,
T6369 12394-12398 NNP denotes NFκB
T6370 12399-12401 VBZ denotes is
T6371 12402-12407 VBN denotes known
T6372 12408-12410 TO denotes to
T6373 12411-12413 VB denotes be
T6374 12414-12423 VBN denotes regulated
T6375 12424-12427 IN denotes via
T6376 12428-12431 NNP denotes DAG
T6377 12432-12435 CC denotes and
T6378 12436-12440 NNP denotes PKCβ
T6379 12441-12442 NNP denotes [
T6380 12442-12447 CD denotes 39,40
T6381 12447-12448 NNP denotes ]
T6382 12449-12452 CC denotes but
T6383 12453-12460 IN denotes whether
T6384 12461-12465 NNS denotes PKDs
T6385 12466-12469 VBP denotes are
T6386 12470-12473 JJ denotes key
T6387 12474-12488 NNS denotes intermediaries
T6388 12489-12492 IN denotes for
T6389 12493-12497 NNP denotes NFκB
T6390 12498-12508 NN denotes regulation
T6391 12509-12512 VBZ denotes has
T6392 12513-12516 RB denotes not
T6393 12517-12521 VBN denotes been
T6394 12522-12530 VBN denotes explored
T6395 12530-12531 . denotes .
T6396 12532-12535 DT denotes The
T6397 12536-12540 NNS denotes data
T6398 12541-12542 -LRB- denotes (
T6399 12542-12546 NNP denotes Fig.
T6400 12547-12549 NNP denotes 4A
T6401 12549-12550 -RRB- denotes )
T6402 12551-12555 VBP denotes show
T6403 12556-12560 IN denotes that
T6404 12561-12565 NNP denotes NFκB
T6405 12566-12581 JJ denotes transcriptional
T6406 12582-12590 NN denotes activity
T6407 12591-12594 VBD denotes was
T6408 12595-12603 RB denotes strongly
T6409 12604-12611 VBN denotes induced
T6410 12612-12614 IN denotes in
T6411 12615-12619 DT denotes both
T6412 12620-12629 JJ denotes wild-type
T6413 12630-12633 CC denotes and
T6414 12634-12640 JJ denotes PKD1/3
T6415 12640-12641 NN denotes
T6416 12641-12642 NN denotes /
T6417 12642-12643 NN denotes
T6418 12644-12648 NNP denotes DT40
T6419 12649-12650 NNP denotes B
T6420 12651-12656 NNS denotes cells
T6421 12657-12659 IN denotes in
T6422 12660-12668 NN denotes response
T6423 12669-12671 TO denotes to
T6424 12672-12678 DT denotes either
T6425 12679-12686 NN denotes phorbol
T6426 12687-12692 NN denotes ester
T6427 12693-12695 CC denotes or
T6428 12696-12699 NNP denotes BCR
T6429 12700-12711 NN denotes stimulation
T6430 12711-12712 . denotes .
T6431 12713-12715 IN denotes In
T6432 12716-12724 NN denotes contrast
T6433 12724-12725 , denotes ,
T6434 12726-12729 NNP denotes BCR
T6435 12730-12733 CC denotes and
T6436 12734-12741 JJ denotes phorbol
T6437 12742-12755 JJ denotes ester-induced
T6438 12756-12760 NNP denotes NFκB
T6439 12761-12776 JJ denotes transcriptional
T6440 12777-12785 NN denotes activity
T6441 12786-12789 VBD denotes was
T6442 12790-12799 VBN denotes abolished
T6443 12800-12802 IN denotes in
T6444 12803-12807 NNP denotes PKCβ
T6445 12807-12808 NNP denotes
T6446 12808-12809 NNP denotes /
T6447 12809-12810 NNP denotes
T6448 12811-12815 NNP denotes DT40
T6449 12816-12817 NNP denotes B
T6450 12818-12823 NNS denotes cells
T6451 12824-12825 -LRB- denotes (
T6452 12825-12829 NNP denotes Fig.
T6453 12830-12832 NNP denotes 4A
T6454 12832-12833 -RRB- denotes )
T6455 12833-12834 , denotes ,
T6456 12835-12843 IN denotes although
T6457 12844-12850 JJ denotes strong
T6458 12851-12861 NN denotes activation
T6459 12862-12864 IN denotes of
T6460 12865-12868 NNP denotes PKD
T6461 12869-12876 NNS denotes kinases
T6462 12877-12878 -LRB- denotes (
T6463 12878-12880 IN denotes as
T6464 12881-12889 VBN denotes assessed
T6465 12890-12892 IN denotes by
T6466 12893-12912 NN denotes autophosphorylation
T6467 12913-12915 IN denotes of
T6468 12916-12920 NNP denotes PKD1
T6469 12921-12923 IN denotes at
T6470 12924-12928 NNP denotes S916
T6471 12928-12929 -RRB- denotes )
T6472 12930-12933 VBD denotes was
T6473 12934-12942 VBN denotes observed
T6474 12943-12945 IN denotes in
T6475 12946-12949 DT denotes the
T6476 12950-12954 NNP denotes PKCβ
T6477 12954-12955 NNP denotes
T6478 12955-12956 VBD denotes /
T6479 12956-12957 CD denotes
T6480 12958-12963 NNS denotes cells
T6481 12964-12965 -LRB- denotes (
T6482 12965-12969 NNP denotes Fig.
T6483 12970-12972 NNP denotes 4B
T6484 12972-12973 -RRB- denotes )
T6485 12973-12974 . denotes .
T6486 12975-12979 RB denotes Thus
T6487 12979-12980 , denotes ,
T6488 12981-12984 NNP denotes PKD
T6489 12985-12992 NNS denotes kinases
T6490 12993-12996 VBP denotes are
T6491 12997-13004 DT denotes neither
T6492 13005-13014 JJ denotes essential
T6493 13015-13018 CC denotes nor
T6494 13019-13029 JJ denotes sufficient
T6495 13030-13032 TO denotes to
T6496 13033-13040 VB denotes mediate
T6497 13041-13052 JJ denotes BCR-induced
T6498 13053-13057 NN denotes NFκB
T6499 13058-13068 NN denotes activation
T6500 13069-13071 IN denotes in
T6501 13072-13076 NNP denotes DT40
T6502 13077-13078 NNP denotes B
T6503 13079-13084 NNS denotes cells
T6504 13085-13088 CC denotes and
T6505 13089-13094 RB denotes hence
T6506 13095-13097 VBP denotes do
T6507 13098-13101 RB denotes not
T6508 13102-13113 VB denotes participate
T6509 13114-13116 IN denotes in
T6510 13117-13124 NNP denotes DAG/PKC
T6511 13125-13133 VBD denotes mediated
T6512 13134-13141 NN denotes control
T6513 13142-13144 IN denotes of
T6514 13145-13149 NNP denotes NFκB
T6515 13149-13150 . denotes .
T7378 13174-13180 NN denotes kinase
T7379 13181-13182 NNP denotes D
T7380 13183-13189 NN denotes serine
T7381 13190-13197 NNS denotes kinases
T7382 13198-13202 VBP denotes have
T7383 13203-13207 VBN denotes been
T7384 13208-13216 VBN denotes proposed
T7385 13217-13219 TO denotes to
T7386 13220-13228 VB denotes regulate
T7387 13229-13236 JJ denotes diverse
T7388 13237-13245 JJ denotes cellular
T7389 13246-13255 NNS denotes functions
T7390 13256-13265 VBG denotes including
T7391 13266-13269 DT denotes the
T7392 13270-13285 NN denotes phosphorylation
T7393 13286-13289 CC denotes and
T7394 13290-13297 JJ denotes nuclear
T7395 13298-13310 NN denotes localisation
T7396 13311-13313 IN denotes of
T7397 13314-13319 NN denotes class
T7398 13320-13322 NNP denotes II
T7399 13323-13328 NNP denotes HDACs
T7400 13329-13332 CC denotes and
T7401 13333-13336 DT denotes the
T7402 13337-13352 NN denotes phosphorylation
T7403 13353-13355 IN denotes of
T7404 13356-13361 NNP denotes HSP27
T7405 13361-13362 . denotes .
T7406 13363-13365 PRP denotes It
T7407 13366-13369 VBZ denotes has
T7408 13370-13374 RB denotes also
T7409 13375-13379 VBN denotes been
T7410 13380-13389 VBN denotes suggested
T7411 13390-13394 IN denotes that
T7412 13395-13399 NNP denotes PKDs
T7413 13400-13403 NN denotes act
T7414 13404-13406 IN denotes as
T7415 13407-13420 JJ denotes mitochondrial
T7416 13421-13428 NNS denotes sensors
T7417 13429-13432 IN denotes for
T7418 13433-13442 JJ denotes oxidative
T7419 13443-13449 NN denotes stress
T7420 13450-13453 CC denotes and
T7421 13454-13458 VB denotes play
T7422 13459-13460 DT denotes a
T7423 13461-13465 NN denotes role
T7424 13466-13468 IN denotes in
T7425 13469-13479 VBG denotes regulating
T7426 13480-13484 NNP denotes NFκB
T7427 13485-13498 NN denotes transcription
T7428 13499-13506 NNS denotes factors
T7429 13507-13508 NNP denotes [
T7430 13508-13510 CD denotes 41
T7431 13510-13511 NNP denotes ]
T7432 13511-13512 . denotes .
T7433 13513-13517 JJS denotes Most
T7434 13518-13520 IN denotes of
T7435 13521-13524 DT denotes the
T7436 13525-13529 NNS denotes data
T7437 13530-13535 IN denotes about
T7438 13536-13539 DT denotes the
T7439 13540-13548 NN denotes function
T7440 13549-13551 IN denotes of
T7441 13552-13556 NNP denotes PKDs
T7442 13557-13560 VBZ denotes has
T7443 13561-13565 VBN denotes come
T7444 13566-13570 IN denotes from
T7445 13571-13582 NNS denotes experiments
T7446 13583-13587 WDT denotes that
T7447 13588-13599 RB denotes ectopically
T7448 13600-13607 VBP denotes express
T7449 13608-13614 JJ denotes active
T7450 13615-13617 CC denotes or
T7451 13618-13628 JJ denotes inhibitory
T7452 13629-13632 NNP denotes PKD
T7453 13633-13640 NNS denotes mutants
T7454 13641-13643 CC denotes or
T7455 13644-13648 DT denotes that
T7456 13649-13652 NN denotes use
T7457 13653-13657 NNS denotes RNAi
T7458 13658-13660 TO denotes to
T7459 13661-13667 VB denotes reduce
T7460 13668-13671 NNP denotes PKD
T7461 13672-13682 NN denotes expression
T7462 13682-13683 . denotes .
T7463 13684-13686 PRP denotes We
T7464 13687-13691 VBP denotes have
T7465 13692-13696 VBN denotes used
T7466 13697-13701 NN denotes gene
T7467 13702-13711 VBG denotes targeting
T7468 13712-13714 TO denotes to
T7469 13715-13727 RB denotes specifically
T7470 13728-13734 VB denotes delete
T7471 13735-13738 NNP denotes PKD
T7472 13739-13746 NNS denotes alleles
T7473 13747-13749 IN denotes in
T7474 13750-13754 NNP denotes DT40
T7475 13755-13762 NN denotes chicken
T7476 13763-13764 NNP denotes B
T7477 13765-13770 NNS denotes cells
T7478 13771-13774 CC denotes and
T7479 13775-13778 MD denotes can
T7480 13779-13783 RB denotes thus
T7481 13784-13787 VB denotes use
T7482 13788-13796 NNP denotes PKD-null
T7483 13797-13801 NNP denotes DT40
T7484 13802-13807 NNS denotes cells
T7485 13808-13810 TO denotes to
T7486 13811-13817 VB denotes assess
T7487 13818-13821 DT denotes the
T7488 13822-13830 JJ denotes relative
T7489 13831-13843 NN denotes contribution
T7490 13844-13846 IN denotes of
T7491 13847-13857 JJ denotes individual
T7492 13858-13861 NNP denotes PKD
T7493 13862-13870 NNS denotes isoforms
T7494 13871-13873 IN denotes in
T7495 13874-13879 NN denotes class
T7496 13880-13882 NNP denotes II
T7497 13883-13887 NNP denotes HDAC
T7498 13888-13895 NN denotes control
T7499 13896-13902 IN denotes versus
T7500 13903-13912 JJ denotes oxidative
T7501 13913-13919 NN denotes stress
T7502 13920-13929 NNS denotes responses
T7503 13930-13933 CC denotes and
T7504 13934-13938 NNP denotes NFκB
T7505 13939-13949 NN denotes regulation
T7506 13950-13952 IN denotes in
T7507 13953-13964 NNS denotes lymphocytes
T7508 13964-13965 . denotes .
T7509 13966-13968 PRP denotes We
T7510 13969-13973 VBP denotes have
T7511 13974-13984 RB denotes previously
T7512 13985-13989 VBN denotes used
T7513 13990-13995 DT denotes these
T7514 13996-14004 NNP denotes PKD-null
T7515 14005-14009 NNP denotes DT40
T7516 14010-14015 NNS denotes cells
T7517 14016-14018 TO denotes to
T7518 14019-14025 VB denotes define
T7519 14026-14028 DT denotes an
T7520 14029-14038 JJ denotes essential
T7521 14039-14043 NN denotes role
T7522 14044-14047 IN denotes for
T7523 14048-14052 NNS denotes PKDs
T7524 14053-14055 IN denotes in
T7525 14056-14066 NN denotes regulation
T7526 14067-14069 IN denotes of
T7527 14070-14075 NN denotes class
T7528 14076-14078 NNP denotes II
T7529 14079-14084 NNP denotes HDACs
T7530 14084-14085 , denotes ,
T7531 14086-14089 DT denotes the
T7532 14090-14097 JJ denotes present
T7533 14098-14104 NN denotes report
T7534 14105-14108 RB denotes now
T7535 14109-14118 VBZ denotes describes
T7536 14119-14121 DT denotes an
T7537 14122-14135 JJ denotes indispensable
T7538 14136-14140 NN denotes role
T7539 14141-14144 IN denotes for
T7540 14145-14149 NNS denotes PKDs
T7541 14150-14152 IN denotes in
T7542 14153-14163 VBG denotes regulating
T7543 14164-14167 DT denotes the
T7544 14168-14183 NN denotes phosphorylation
T7545 14184-14186 IN denotes of
T7546 14187-14192 NNP denotes HSP27
T7547 14193-14195 IN denotes on
T7548 14196-14202 NN denotes serine
T7549 14203-14205 CD denotes 82
T7550 14205-14206 , denotes ,
T7551 14207-14208 DT denotes a
T7552 14209-14213 NN denotes site
T7553 14214-14224 RB denotes previously
T7554 14225-14235 VBN denotes identified
T7555 14236-14238 IN denotes as
T7556 14239-14240 DT denotes a
T7557 14241-14247 NN denotes target
T7558 14248-14251 IN denotes for
T7559 14252-14255 DT denotes the
T7560 14256-14268 NN denotes p38-MAPKAPK2
T7561 14269-14279 VBG denotes signalling
T7562 14280-14287 NN denotes cascade
T7563 14288-14289 NNP denotes [
T7564 14289-14291 CD denotes 42
T7565 14291-14292 NNP denotes ]
T7566 14292-14293 . denotes .
T7567 14294-14301 RB denotes However
T7568 14301-14302 , denotes ,
T7569 14303-14310 NNS denotes studies
T7570 14311-14313 IN denotes of
T7571 14314-14322 NNP denotes PKD-null
T7572 14323-14327 NNP denotes DT40
T7573 14328-14333 NNS denotes cells
T7574 14334-14340 VBP denotes reveal
T7575 14341-14345 IN denotes that
T7576 14346-14349 NNP denotes PKD
T7577 14350-14356 NN denotes family
T7578 14357-14364 NNS denotes kinases
T7579 14365-14368 VBP denotes are
T7580 14369-14372 RB denotes not
T7581 14373-14382 JJ denotes essential
T7582 14383-14386 IN denotes for
T7583 14387-14396 JJ denotes oxidative
T7584 14397-14403 NN denotes stress
T7585 14404-14412 NN denotes survival
T7586 14413-14422 NNS denotes responses
T7587 14423-14426 CC denotes nor
T7588 14427-14430 VBP denotes are
T7589 14431-14435 PRP denotes they
T7590 14436-14444 VBN denotes required
T7591 14445-14448 IN denotes for
T7592 14449-14459 NN denotes activation
T7593 14460-14462 IN denotes of
T7594 14463-14467 NNP denotes NFκB
T7595 14468-14481 NN denotes transcription
T7596 14482-14489 NNS denotes factors
T7597 14489-14490 . denotes .
T7598 14491-14496 DT denotes These
T7599 14497-14503 JJ denotes latter
T7600 14504-14512 NNS denotes findings
T7601 14513-14516 VBP denotes are
T7602 14517-14519 IN denotes in
T7603 14520-14528 JJ denotes striking
T7604 14529-14537 NN denotes contrast
T7605 14538-14540 TO denotes to
T7606 14541-14549 JJ denotes previous
T7607 14550-14562 NNS denotes observations
T7608 14563-14565 IN denotes in
T7609 14566-14570 NNP denotes HeLa
T7610 14571-14574 CC denotes and
T7611 14575-14585 JJ denotes epithelial
T7612 14586-14590 NN denotes cell
T7613 14591-14596 NNS denotes lines
T7614 14597-14602 WRB denotes where
T7615 14603-14622 NNP denotes overexpression/RNAi
T7616 14623-14633 NNS denotes approaches
T7617 14634-14638 VBP denotes have
T7618 14639-14649 VBN denotes implicated
T7619 14650-14656 NNP denotes PKD1/2
T7620 14657-14659 IN denotes in
T7621 14660-14663 DT denotes the
T7622 14664-14671 NN denotes control
T7623 14672-14674 IN denotes of
T7624 14675-14688 NN denotes proliferation
T7625 14688-14689 , denotes ,
T7626 14690-14698 NN denotes survival
T7627 14699-14702 CC denotes and
T7628 14703-14707 NNP denotes NFκB
T7629 14708-14718 NN denotes activation
T7630 14719-14720 NNP denotes [
T7631 14720-14725 CD denotes 20,23
T7632 14725-14726 NNP denotes ]
T7633 14726-14727 . denotes .
T7634 14728-14733 RB denotes Hence
T7635 14733-14734 , denotes ,
T7636 14735-14738 DT denotes the
T7637 14739-14746 JJ denotes present
T7638 14747-14753 NN denotes report
T7639 14754-14759 VBZ denotes shows
T7640 14760-14764 IN denotes that
T7641 14765-14768 DT denotes the
T7642 14769-14777 VBN denotes proposed
T7643 14778-14783 NNS denotes roles
T7644 14784-14787 IN denotes for
T7645 14788-14792 NNS denotes PKDs
T7646 14793-14795 IN denotes as
T7647 14796-14799 JJ denotes key
T7648 14800-14807 NNS denotes sensors
T7649 14808-14812 WDT denotes that
T7650 14813-14821 VBP denotes modulate
T7651 14822-14830 NN denotes survival
T7652 14831-14839 NNS denotes pathways
T7653 14840-14842 IN denotes in
T7654 14843-14851 NN denotes response
T7655 14852-14854 TO denotes to
T7656 14855-14864 JJ denotes oxidative
T7657 14865-14871 NN denotes stress
T7658 14872-14875 CC denotes and
T7659 14876-14884 VB denotes regulate
T7660 14885-14889 NN denotes cell
T7661 14890-14898 NN denotes survival
T7662 14899-14902 CC denotes and
T7663 14903-14916 NN denotes proliferation
T7664 14917-14920 VBP denotes are
T7665 14921-14924 RB denotes not
T7666 14925-14935 JJ denotes ubiquitous
T7667 14936-14939 CC denotes and
T7668 14940-14943 MD denotes may
T7669 14944-14946 VB denotes be
T7670 14947-14957 VBN denotes restricted
T7671 14958-14960 TO denotes to
T7672 14961-14968 JJ denotes certain
T7673 14969-14973 NN denotes cell
T7674 14974-14982 NNS denotes lineages
T7675 14982-14983 . denotes .
T7676 14984-14989 VBN denotes Taken
T7677 14990-14998 RB denotes together
T7678 14998-14999 , denotes ,
T7679 15000-15005 DT denotes these
T7680 15006-15010 NNS denotes data
T7681 15011-15019 VBP denotes indicate
T7682 15020-15024 IN denotes that
T7683 15025-15029 NN denotes loss
T7684 15030-15032 IN denotes of
T7685 15033-15043 NN denotes expression
T7686 15044-15046 IN denotes of
T7687 15047-15050 NNP denotes PKD
T7688 15051-15057 NN denotes family
T7689 15058-15065 NNS denotes members
T7690 15066-15070 VBZ denotes does
T7691 15071-15074 RB denotes not
T7692 15075-15083 RB denotes globally
T7693 15084-15090 NN denotes impact
T7694 15091-15093 IN denotes on
T7695 15094-15099 JJ denotes early
T7696 15100-15113 JJ denotes BCR-regulated
T7697 15114-15124 NN denotes signalling
T7698 15125-15133 NNS denotes pathways
T7699 15133-15134 . denotes .
R1000 T1114 T1071 punct .,involves
R1001 T1115 T1118 det The,region
R1002 T1116 T1118 amod N-terminal,region
R1003 T1117 T1118 amod regulatory,region
R1004 T1118 T1121 nsubj region,enzymes
R1005 T1119 T1118 prep of,region
R1006 T1120 T1119 pobj PKD,of
R1007 T1121 T1121 ROOT enzymes,enzymes
R1008 T1122 T1121 conj contains,enzymes
R1009 T1123 T1124 det a,DAG
R1010 T1124 T1126 nmod DAG,domain
R1011 T1125 T1126 amod binding,domain
R1012 T1126 T1122 dobj domain,contains
R1013 T1127 T1126 cc and,domain
R1014 T1128 T1129 amod direct,binding
R1015 T1129 T1126 conj binding,domain
R1016 T1130 T1129 prep of,binding
R1017 T1131 T1130 pobj DAG,of
R1018 T1132 T1133 advmod also,contributes
R1019 T1133 T1121 conj contributes,enzymes
R1020 T1134 T1133 prep to,contributes
R1021 T1135 T1139 nummod PKD1,]
R1022 T1136 T1137 compound activation,[
R1023 T1137 T1139 nmod [,]
R1024 T1138 T1137 nummod 7,[
R1025 T1139 T1134 pobj ],to
R1026 T1140 T1142 advmod as,as
R1027 T1141 T1142 advmod well,as
R1028 T1142 T1133 prep as,contributes
R1029 T1143 T1142 pcomp regulating,as
R1030 T1144 T1146 det the,location
R1031 T1145 T1146 amod spatial,location
R1032 T1146 T1143 dobj location,regulating
R1033 T1147 T1146 prep of,location
R1034 T1148 T1149 compound PKD,enzymes
R1035 T1149 T1147 pobj enzymes,of
R1036 T1150 T1143 prep within,regulating
R1037 T1151 T1150 pobj cells,within
R1038 T1152 T1153 nmod [,8
R1039 T1153 T1143 npadvmod 8,regulating
R1040 T1154 T1155 nummod 12,]
R1041 T1155 T1153 appos ],8
R1042 T1156 T1121 punct .,enzymes
R1043 T1157 T1158 compound PKD,enzymes
R1044 T1158 T1161 nsubjpass enzymes,proposed
R1045 T1159 T1161 aux have,proposed
R1046 T1160 T1161 auxpass been,proposed
R1047 T1161 T1161 ROOT proposed,proposed
R1048 T1162 T1163 aux to,regulate
R1049 T1163 T1161 xcomp regulate,proposed
R1050 T1164 T1166 amod numerous,functions
R1051 T1165 T1166 amod cellular,functions
R1052 T1166 T1163 dobj functions,regulate
R1053 T1167 T1166 punct ",",functions
R1054 T1168 T1166 prep including,functions
R1055 T1169 T1170 compound cell,proliferation
R1056 T1170 T1168 pobj proliferation,including
R1057 T1171 T1170 dobj [,proliferation
R1058 T1172 T1171 nummod 13,[
R1059 T1173 T1174 nummod 16,]
R1060 T1174 T1171 appos ],[
R1061 T1175 T1177 punct ",",signals
R1062 T1176 T1177 amod anti-apoptotic,signals
R1063 T1177 T1171 appos signals,[
R1064 T1178 T1180 compound [,]
R1065 T1179 T1180 compound "17,18",]
R1066 T1180 T1177 dobj ],signals
R1067 T1181 T1180 cc and,]
R1068 T1182 T1183 amod thymocyte,development
R1069 T1183 T1186 nmod development,]
R1070 T1184 T1186 nmod [,]
R1071 T1185 T1186 nummod 19,]
R1072 T1186 T1180 conj ],]
R1073 T1187 T1177 punct .,signals
R1074 T1188 T1199 nsubj Expression,modify
R1075 T1189 T1188 prep of,Expression
R1076 T1190 T1192 amod mutant,inactive
R1077 T1191 T1192 advmod catalytically,inactive
R1078 T1192 T1196 amod inactive,PKDs
R1079 T1193 T1192 cc and,inactive
R1080 T1194 T1195 advmod constitutively,activated
R1081 T1195 T1192 conj activated,inactive
R1082 T1196 T1188 appos PKDs,Expression
R1083 T1197 T1199 aux can,modify
R1084 T1198 T1199 advmod also,modify
R1085 T1199 T1199 ROOT modify,modify
R1086 T1200 T1201 compound Golgi,function
R1087 T1201 T1199 dobj function,modify
R1088 T1202 T1201 punct ",",function
R1089 T1203 T1204 compound cell,adhesion
R1090 T1204 T1201 conj adhesion,function
R1091 T1205 T1204 cc and,adhesion
R1092 T1206 T1207 compound cell,motility
R1093 T1207 T1204 conj motility,adhesion
R1094 T1208 T1209 punct (,reviewed
R1095 T1209 T1199 advcl reviewed,modify
R1096 T1210 T1209 prep in,reviewed
R1097 T1211 T1210 pobj [,in
R1098 T1212 T1213 nummod 20,]
R1099 T1213 T1211 appos ],[
R1100 T1214 T1211 punct ),[
R1101 T1215 T1199 punct .,modify
R1102 T1216 T1223 prep In,linked
R1103 T1217 T1216 amod particular,In
R1104 T1218 T1223 punct ",",linked
R1105 T1219 T1223 nsubjpass PKDs,linked
R1106 T1220 T1223 aux have,linked
R1107 T1221 T1223 auxpass been,linked
R1108 T1222 T1223 advmod widely,linked
R1109 T1223 T1223 ROOT linked,linked
R1110 T1224 T1223 prep to,linked
R1111 T1225 T1226 det the,activation
R1112 T1226 T1224 pobj activation,to
R1113 T1227 T1226 prep of,activation
R1114 T1228 T1231 det the,factor
R1115 T1229 T1231 compound NFκB,factor
R1116 T1230 T1231 compound transcription,factor
R1117 T1231 T1227 pobj factor,of
R1118 T1232 T1224 cc and,to
R1119 T1233 T1223 prep in,linked
R1120 T1234 T1233 pcomp regulating,in
R1121 T1235 T1236 compound cell,survival
R1122 T1236 T1234 dobj survival,regulating
R1123 T1237 T1234 prep during,regulating
R1124 T1238 T1239 amod oxidative,stress
R1125 T1239 T1241 compound stress,"17,21"
R1126 T1240 T1241 compound [,"17,21"
R1127 T1241 T1237 pobj "17,21",during
R1128 T1242 T1243 nummod 23,]
R1129 T1243 T1243 ROOT ],]
R1130 T1244 T1223 punct .,linked
R1131 T1245 T1249 det Another,substrate
R1132 T1246 T1247 advmod recently,proposed
R1133 T1247 T1249 amod proposed,substrate
R1134 T1248 T1249 compound PKD1,substrate
R1135 T1249 T1250 nsubj substrate,is
R1136 T1250 T1250 ROOT is,is
R1137 T1251 T1252 compound HSP27,[
R1138 T1252 T1250 attr [,is
R1139 T1253 T1254 nummod 24,]
R1140 T1254 T1252 appos ],[
R1141 T1255 T1254 punct ",",]
R1142 T1256 T1260 det a,protein
R1143 T1257 T1260 amod small,protein
R1144 T1258 T1259 compound heat,shock
R1145 T1259 T1260 compound shock,protein
R1146 T1260 T1254 appos protein,]
R1147 T1261 T1260 amod involved,protein
R1148 T1262 T1261 prep in,involved
R1149 T1263 T1262 pcomp regulating,in
R1150 T1264 T1265 compound cell,migration
R1151 T1265 T1263 dobj migration,regulating
R1152 T1266 T1265 cc and,migration
R1153 T1267 T1268 compound cell,survival
R1154 T1268 T1265 conj survival,migration
R1155 T1269 T1271 nmod [,]
R1156 T1270 T1271 nummod 25,]
R1157 T1271 T1265 appos ],migration
R1158 T1272 T1250 punct .,is
R1159 T1273 T1275 det An,role
R1160 T1274 T1275 amod essential,role
R1161 T1275 T1289 nsubj role,enzymes
R1162 T1276 T1275 prep for,role
R1163 T1277 T1278 compound PKD,enzymes
R1164 T1278 T1276 pobj enzymes,for
R1165 T1279 T1278 prep in,enzymes
R1166 T1280 T1279 pcomp regulating,in
R1167 T1281 T1284 nmod class,deacetylases
R1168 T1282 T1281 nummod II,class
R1169 T1283 T1284 compound histone,deacetylases
R1170 T1284 T1280 dobj deacetylases,regulating
R1171 T1285 T1284 punct (,deacetylases
R1172 T1286 T1284 appos HDACs,deacetylases
R1173 T1287 T1284 punct ),deacetylases
R1174 T1288 T1278 punct ",",enzymes
R1175 T1289 T1289 ROOT enzymes,enzymes
R1176 T1290 T1291 mark that,repress
R1177 T1291 T1289 ccomp repress,enzymes
R1178 T1292 T1294 amod MEF2-dependent,transcription
R1179 T1293 T1294 compound gene,transcription
R1180 T1294 T1291 dobj transcription,repress
R1181 T1295 T1299 punct ",",demonstrated
R1182 T1296 T1299 aux has,demonstrated
R1183 T1297 T1299 advmod also,demonstrated
R1184 T1298 T1299 auxpass been,demonstrated
R1185 T1299 T1289 conj demonstrated,enzymes
R1186 T1300 T1301 compound [,"1,26"
R1187 T1301 T1299 dobj "1,26",demonstrated
R1188 T1302 T1303 nummod 28,]
R1189 T1303 T1299 npadvmod ],demonstrated
R1190 T1304 T1299 punct .,demonstrated
R1191 T1305 T1306 aux To,investigate
R1192 T1306 T1314 advcl investigate,generated
R1193 T1307 T1309 det the,role
R1194 T1308 T1309 amod biological,role
R1195 T1309 T1306 dobj role,investigate
R1196 T1310 T1309 prep of,role
R1197 T1311 T1310 pobj PKDs,of
R1198 T1312 T1314 nsubj we,generated
R1199 T1313 T1314 aux have,generated
R1200 T1314 T1314 ROOT generated,generated
R1201 T1315 T1318 compound DT40,lines
R1202 T1316 T1318 compound B,lines
R1203 T1317 T1318 compound cell,lines
R1204 T1318 T1314 dobj lines,generated
R1205 T1319 T1320 nsubj that,lack
R1206 T1320 T1318 relcl lack,lines
R1207 T1321 T1320 dobj expression,lack
R1208 T1322 T1321 prep of,expression
R1209 T1323 T1326 nummod one,members
R1210 T1324 T1323 cc or,one
R1211 T1325 T1323 conj more,one
R1212 T1326 T1322 pobj members,of
R1213 T1327 T1326 prep of,members
R1214 T1328 T1330 det the,family
R1215 T1329 T1330 compound PKD,family
R1216 T1330 T1327 pobj family,of
R1217 T1331 T1333 nmod [,]
R1218 T1332 T1333 nummod 1,]
R1219 T1333 T1326 appos ],members
R1220 T1334 T1314 punct ",",generated
R1221 T1335 T1314 advcl allowing,generated
R1222 T1336 T1338 nsubj us,investigate
R1223 T1337 T1338 aux to,investigate
R1224 T1338 T1335 ccomp investigate,allowing
R1225 T1339 T1340 det the,function
R1226 T1340 T1338 dobj function,investigate
R1227 T1341 T1340 punct (,function
R1228 T1342 T1340 appos s,function
R1229 T1343 T1340 punct ),function
R1230 T1344 T1340 prep of,function
R1231 T1345 T1344 pobj PKD,of
R1232 T1346 T1344 pobj isoforms,of
R1233 T1347 T1346 acl following,isoforms
R1234 T1348 T1350 compound B,antigen
R1235 T1349 T1350 compound cell,antigen
R1236 T1350 T1351 compound antigen,receptor
R1237 T1351 T1347 dobj receptor,following
R1238 T1352 T1353 punct (,BCR
R1239 T1353 T1351 appos BCR,receptor
R1240 T1354 T1353 punct ),BCR
R1241 T1355 T1351 conj stimulation,receptor
R1242 T1356 T1347 punct ",",following
R1243 T1357 T1359 advmod as,addressing
R1244 T1358 T1359 advmod well,addressing
R1245 T1359 T1338 advcl addressing,investigate
R1246 T1360 T1361 det the,issue
R1247 T1361 T1359 dobj issue,addressing
R1248 T1362 T1361 prep of,issue
R1249 T1363 T1364 amod functional,redundancy
R1250 T1364 T1362 pobj redundancy,of
R1251 T1365 T1364 prep between,redundancy
R1252 T1366 T1370 det the,members
R1253 T1367 T1370 amod different,members
R1254 T1368 T1370 compound PKD,members
R1255 T1369 T1370 compound family,members
R1256 T1370 T1365 pobj members,between
R1257 T1371 T1314 punct .,generated
R1258 T1372 T1373 amod Previous,studies
R1259 T1373 T1375 nsubj studies,shown
R1260 T1448 T1449 amod transcriptional,activity
R1261 T1374 T1375 aux have,shown
R1262 T1449 T1446 dobj activity,regulating
R1263 T1450 T1441 punct .,play
R1264 T1375 T1375 ROOT shown,shown
R1265 T1451 T1455 advmod Together,reveal
R1266 T1452 T1455 punct ",",reveal
R1267 T1376 T1378 mark that,are
R1268 T1453 T1454 det these,findings
R1269 T1454 T1455 nsubj findings,reveal
R1270 T1455 T1455 ROOT reveal,reveal
R1271 T1456 T1463 mark that,are
R1272 T1457 T1463 prep in,are
R1273 T1458 T1459 compound B,lymphocytes
R1274 T1459 T1457 pobj lymphocytes,in
R1275 T1377 T1378 nsubj PKDs,are
R1276 T1460 T1463 punct ",",are
R1277 T1461 T1462 compound PKD,kinases
R1278 T1462 T1463 nsubj kinases,are
R1279 T1378 T1375 ccomp are,shown
R1280 T1463 T1455 ccomp are,reveal
R1281 T1464 T1463 neg not,are
R1282 T1465 T1466 amod critical,regulators
R1283 T1466 T1463 attr regulators,are
R1284 T1379 T1378 acomp indispensable,are
R1285 T1467 T1466 prep of,regulators
R1286 T1468 T1467 pobj many,of
R1287 T1469 T1468 prep of,many
R1288 T1380 T1378 prep for,are
R1289 T1470 T1472 det the,processes
R1290 T1471 T1472 amod cellular,processes
R1291 T1472 T1469 pobj processes,of
R1292 T1381 T1382 compound HDAC,regulation
R1293 T1473 T1474 advmod previously,ascribed
R1294 T1474 T1463 conj ascribed,are
R1295 T1475 T1474 prep to,ascribed
R1296 T1382 T1380 pobj regulation,for
R1297 T1476 T1475 pobj them,to
R1298 T1383 T1382 prep in,regulation
R1299 T1477 T1474 prep in,ascribed
R1300 T1478 T1480 amod other,systems
R1301 T1479 T1480 amod cellular,systems
R1302 T1480 T1477 pobj systems,in
R1303 T1384 T1385 compound B,cells
R1304 T1481 T1455 punct .,reveal
R1305 T1385 T1383 pobj cells,in
R1306 T1386 T1388 nmod [,]
R1307 T1387 T1388 nummod 1,]
R1308 T1388 T1382 appos ],regulation
R1309 T1389 T1375 punct .,shown
R1310 T1390 T1392 npadvmod Herein,show
R1311 T1391 T1392 nsubj we,show
R1312 T1392 T1392 ROOT show,show
R1313 T1393 T1395 mark that,are
R1314 T1394 T1395 nsubj PKDs,are
R1315 T1395 T1392 ccomp are,show
R1316 T1396 T1395 advmod also,are
R1317 T1397 T1395 acomp indispensable,are
R1318 T1398 T1395 prep for,are
R1319 T1399 T1400 compound HSP27,phosphorylation
R1320 T1400 T1398 pobj phosphorylation,for
R1321 T1401 T1400 prep in,phosphorylation
R1322 T1402 T1403 compound B,cells
R1323 T1403 T1401 pobj cells,in
R1324 T1404 T1392 punct .,show
R1325 T1405 T1411 advmod However,are
R1326 T1406 T1411 punct ",",are
R1327 T1407 T1409 compound PKD-null,B
R1328 T1408 T1409 compound DT40,B
R1329 T1409 T1410 compound B,cells
R1331 T1410 T1411 nsubj cells,are
R1335 T1411 T1411 ROOT are,are
R1336 T1412 T1411 acomp viable,are
R1338 T1413 T1411 cc and,are
R1340 T1414 T1411 conj proliferate,are
R1341 T1415 T1414 advmod normally,proliferate
R1342 T1416 T1411 punct .,are
R1343 T1417 T1430 advmod Moreover,affect
R1344 T1418 T1430 punct ",",affect
R1345 T1419 T1430 nsubj loss,affect
R1347 T1420 T1419 prep of,loss
R1351 T1421 T1424 det the,pool
R1352 T1422 T1424 amod entire,pool
R1355 T1423 T1424 amod cellular,pool
R1356 T1424 T1420 pobj pool,of
R1357 T1425 T1424 prep of,pool
R1358 T1426 T1425 pobj PKD,of
R1359 T1427 T1430 aux does,affect
R1360 T1428 T1430 neg not,affect
R1361 T1429 T1430 advmod critically,affect
R1362 T1430 T1430 ROOT affect,affect
R1365 T1431 T1433 amod oxidative,responses
R1367 T1432 T1433 compound stress,responses
R1369 T1433 T1430 dobj responses,affect
R1371 T1434 T1433 prep in,responses
R1373 T1435 T1436 compound B,cells
R1374 T1436 T1434 pobj cells,in
R1376 T1437 T1430 cc nor,affect
R1378 T1438 T1441 aux do,play
R1379 T1439 T1440 compound PKD,kinases
R1380 T1440 T1441 nsubj kinases,play
R1381 T1441 T1430 conj play,affect
R1382 T1442 T1444 det an,role
R1383 T1443 T1444 amod essential,role
R1384 T1444 T1441 dobj role,play
R1385 T1445 T1444 prep in,role
R1387 T1446 T1445 pcomp regulating,in
R1391 T1447 T1449 nmod NFκB,activity
R1502 T1742 T1744 nummod "Protein kinase D enzymes are dispensable for proliferation, survival and antigen receptor-regulated NFκB activity in vertebrate B-cells Abstract To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. Most cell types express at least two PKD isoforms but PKD enzymes are especially highly expressed in haematopoietic cells, where they are activated in response to antigen receptors stimulation [2,3]. A conserved signalling pathway linking antigen receptors to PKDs involves the activation of PLCγ and the subsequent production of diacylglycerol (DAG) which stimulates classical and/or novel protein kinase Cs (PKC) that phosphorylate two key regulatory serine residues in the activation loop of PKD kinases [3–6]. The N-terminal regulatory region of PKD enzymes contains a DAG binding domain and direct binding of DAG also contributes to PKD1 activation [7] as well as regulating the spatial location of PKD enzymes within cells [8–12]. PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). In particular, PKDs have been widely linked to the activation of the NFκB transcription factor and in regulating cell survival during oxidative stress [17,21–23]. Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. An essential role for PKD enzymes in regulating class II histone deacetylases (HDACs), enzymes that repress MEF2-dependent gene transcription, has also been demonstrated [1,26–28]. To investigate the biological role of PKDs we have generated DT40 B cell lines that lack expression of one or more members of the PKD family [1], allowing us to investigate the function(s) of PKD isoforms following B cell antigen receptor (BCR) stimulation, as well addressing the issue of functional redundancy between the different PKD family members. Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. However, PKD-null DT40 B cells are viable and proliferate normally. Moreover, loss of the entire cellular pool of PKD does not critically affect oxidative stress responses in B cells nor do PKD kinases play an essential role in regulating NFκB transcriptional activity. Together, these findings reveal that in B lymphocytes, PKD kinases are not critical regulators of many of the cellular processes previously ascribed to them in other cellular systems. 2 Materials and methods 2.1 ",culture
R1503 T1743 T1744 compound Cell,culture
R1504 T1744 T1744 ROOT culture,culture
R1505 T1745 T1744 punct ",",culture
R1506 T1746 T1747 compound transient,transfections
R1507 T1747 T1744 appos transfections,culture
R1508 T1748 T1747 cc and,transfections
R1509 T1749 T1750 compound cell,stimulation
R1510 T1750 T1747 conj stimulation,transfections
R1511 T1751 T1752 det The,generation
R1512 T1752 T1765 nsubj generation,/
R1513 T1753 T1752 punct ",",generation
R1514 T1754 T1752 conj culture,generation
R1515 T1755 T1754 cc and,culture
R1516 T1756 T1754 conj activation,culture
R1517 T1757 T1752 prep of,generation
R1518 T1758 T1761 nummod PKD1,−
R1519 T1759 T1761 nummod −,−
R1520 T1760 T1761 compound /,−
R1521 T1761 T1757 pobj −,of
R1522 T1762 T1765 punct ",",/
R1523 T1763 T1764 compound PKD3,−
R1524 T1764 T1765 nsubj −,/
R1525 T1765 T1765 ROOT /,/
R1526 T1766 T1776 nummod −,lines
R1527 T1767 T1766 cc and,−
R1528 T1768 T1776 nummod PKD1/3,lines
R1529 T1769 T1776 nummod −,lines
R1530 T1770 T1772 nmod /,knockout
R1531 T1771 T1772 compound −,knockout
R1532 T1772 T1776 compound knockout,lines
R1533 T1773 T1774 compound DT40,B
R1534 T1774 T1775 compound B,cell
R1535 T1775 T1776 compound cell,lines
R1536 T1776 T1779 nsubjpass lines,described
R1537 T1777 T1779 aux have,described
R1538 T1778 T1779 auxpass been,described
R1539 T1779 T1765 ccomp described,/
R1540 T1780 T1783 advmod previously,]
R1541 T1781 T1783 nmod [,]
R1542 T1782 T1781 nummod 1,[
R1543 T1783 T1779 dobj ],described
R1544 T1784 T1765 punct .,/
R1545 T1785 T1787 nsubjpass Cells,lysed
R1546 T1786 T1787 auxpass were,lysed
R1547 T1787 T1787 ROOT lysed,lysed
R1548 T1788 T1787 cc and,lysed
R1549 T1789 T1790 compound protein,extracts
R1550 T1790 T1792 nsubjpass extracts,analysed
R1551 T1791 T1792 auxpass were,analysed
R1552 T1792 T1787 conj analysed,lysed
R1553 T1793 T1792 prep in,analysed
R1554 T1794 T1796 amod Western,experiments
R1555 T1795 T1796 amod blotting,experiments
R1556 T1796 T1793 pobj experiments,in
R1557 T1797 T1799 mark as,described
R1558 T1798 T1799 advmod previously,described
R1559 T1799 T1792 advcl described,analysed
R1560 T1800 T1802 nmod [,]
R1561 T1801 T1802 nummod 1,]
R1562 T1802 T1799 dobj ],described
R1563 T1803 T1792 punct .,analysed
R1564 T1804 T1807 nmod Chloramphenicol,assays
R1565 T1805 T1807 nmod acetyl,assays
R1566 T1806 T1807 compound transferase,assays
R1567 T1807 T1810 nsubjpass assays,described
R1568 T1808 T1810 aux have,described
R1569 T1809 T1810 auxpass been,described
R1570 T1810 T1810 ROOT described,described
R1571 T1811 T1814 advmod previously,]
R1572 T1812 T1814 nmod [,]
R1573 T1813 T1814 nummod 29,]
R1574 T1814 T1810 dobj ],described
R1575 T1815 T1810 punct .,described
R1663 T1939 T1940 nummod "Protein kinase D enzymes are dispensable for proliferation, survival and antigen receptor-regulated NFκB activity in vertebrate B-cells Abstract To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. Most cell types express at least two PKD isoforms but PKD enzymes are especially highly expressed in haematopoietic cells, where they are activated in response to antigen receptors stimulation [2,3]. A conserved signalling pathway linking antigen receptors to PKDs involves the activation of PLCγ and the subsequent production of diacylglycerol (DAG) which stimulates classical and/or novel protein kinase Cs (PKC) that phosphorylate two key regulatory serine residues in the activation loop of PKD kinases [3–6]. The N-terminal regulatory region of PKD enzymes contains a DAG binding domain and direct binding of DAG also contributes to PKD1 activation [7] as well as regulating the spatial location of PKD enzymes within cells [8–12]. PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). In particular, PKDs have been widely linked to the activation of the NFκB transcription factor and in regulating cell survival during oxidative stress [17,21–23]. Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. An essential role for PKD enzymes in regulating class II histone deacetylases (HDACs), enzymes that repress MEF2-dependent gene transcription, has also been demonstrated [1,26–28]. To investigate the biological role of PKDs we have generated DT40 B cell lines that lack expression of one or more members of the PKD family [1], allowing us to investigate the function(s) of PKD isoforms following B cell antigen receptor (BCR) stimulation, as well addressing the issue of functional redundancy between the different PKD family members. Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. However, PKD-null DT40 B cells are viable and proliferate normally. Moreover, loss of the entire cellular pool of PKD does not critically affect oxidative stress responses in B cells nor do PKD kinases play an essential role in regulating NFκB transcriptional activity. Together, these findings reveal that in B lymphocytes, PKD kinases are not critical regulators of many of the cellular processes previously ascribed to them in other cellular systems. 2 Materials and methods 2.1 Cell culture, transient transfections and cell stimulation The generation, culture and activation of PKD1−/−, PKD3−/− and PKD1/3−/− knockout DT40 B cell lines have been described previously [1]. Cells were lysed and protein extracts were analysed in Western blotting experiments as previously described [1]. Chloramphenicol acetyl transferase assays have been described previously [29]. 2.2 ",sIgM
R1664 T1940 T1944 amod sIgM,cells
R1665 T1941 T1944 amod staining,cells
R1666 T1942 T1943 compound DT40,B
R1667 T1943 T1944 compound B,cells
R1668 T1944 T1954 nsubjpass cells,resuspended
R1669 T1945 T1944 punct (,cells
R1670 T1946 T1949 nummod 2,cells
R1671 T1947 T1949 nummod ×,cells
R1672 T1948 T1949 nummod 106,cells
R1673 T1949 T1944 appos cells,cells
R1674 T1950 T1949 prep per,cells
R1675 T1951 T1950 pobj point,per
R1676 T1952 T1944 punct ),cells
R1677 T1953 T1954 auxpass were,resuspended
R1678 T1954 T1954 ROOT resuspended,resuspended
R1679 T1955 T1954 prep in,resuspended
R1680 T1956 T1958 nummod 200,buffer
R1681 T1957 T1958 compound μl,buffer
R1682 T1958 T1955 pobj buffer,in
R1683 T1959 T1958 punct (,buffer
R1684 T1960 T1962 compound RPMI,media
R1685 T1961 T1962 compound 1640,media
R1686 T1962 T1958 appos media,buffer
R1687 T1963 T1962 punct ",",media
R1688 T1964 T1965 nummod 1,%
R1689 T1965 T1968 nmod %,serum
R1690 T1966 T1968 amod foetal,serum
R1691 T1967 T1968 compound calf,serum
R1692 T1968 T1962 appos serum,media
R1693 T1969 T1962 punct ),media
R1694 T1970 T1958 acl containing,buffer
R1695 T1971 T1975 amod anti-chicken,conjugated
R1696 T1972 T1974 nummod M1,antibody
R1697 T1973 T1974 amod monoclonal,antibody
R1698 T1974 T1975 compound antibody,conjugated
R1699 T1975 T1954 conj conjugated,resuspended
R1700 T1976 T1975 prep to,conjugated
R1701 T1977 T1976 pobj FITC,to
R1702 T1978 T1975 prep for,conjugated
R1703 T1979 T1980 nummod 20,min
R1704 T1980 T1978 pobj min,for
R1705 T1981 T1980 prep on,min
R1706 T1982 T1981 pobj ice,on
R1707 T1983 T1954 punct .,resuspended
R1708 T1984 T1985 det The,cells
R1709 T1985 T1987 nsubjpass cells,washed
R1710 T1986 T1987 auxpass were,washed
R1711 T1987 T1987 ROOT washed,washed
R1712 T1988 T1987 advmod twice,washed
R1713 T1989 T1988 cc and,twice
R1714 T1990 T1991 amod fluorescent,intensity
R1715 T1991 T1993 nsubjpass intensity,analysed
R1716 T1992 T1993 auxpass was,analysed
R1717 T1993 T1987 conj analysed,washed
R1718 T1994 T1993 agent by,analysed
R1719 T1995 T1996 compound flow,cytometry
R1720 T1996 T1994 pobj cytometry,by
R1721 T1997 T1993 punct .,analysed
R1722 T1998 T1999 det All,results
R1723 T1999 T2001 nsubj results,are
R1724 T2000 T1999 acl shown,results
R1725 T2001 T2001 ROOT are,are
R1726 T2002 T2001 attr representative,are
R1727 T2003 T2002 prep of,representative
R1728 T2004 T2001 prep at,are
R1729 T2005 T2007 quantmod two,four
R1730 T2006 T2007 quantmod to,four
R1731 T2007 T2009 nummod four,experiments
R1732 T2008 T2009 amod independent,experiments
R1733 T2009 T2004 pobj experiments,at
R1734 T2010 T2012 mark unless,indicated
R1735 T2011 T2012 advmod otherwise,indicated
R1736 T2012 T2001 advcl indicated,are
R1737 T2013 T2001 punct .,are
R175 T212 T215 compound Protein,enzymes
R176 T213 T215 compound kinase,enzymes
R177 T214 T215 compound D,enzymes
R178 T215 T216 nsubj enzymes,are
R179 T216 T216 ROOT are,are
R180 T217 T216 acomp dispensable,are
R181 T218 T217 prep for,dispensable
R182 T219 T226 nmod proliferation,activity
R183 T220 T219 punct ",",proliferation
R184 T221 T219 conj survival,proliferation
R185 T222 T221 cc and,survival
R186 T223 T221 conj antigen,survival
R187 T224 T226 amod receptor-regulated,activity
R188 T225 T226 compound NFκB,activity
R189 T226 T218 pobj activity,for
R190 T227 T226 prep in,activity
R191 T228 T229 amod vertebrate,B-cells
R192 T229 T227 pobj B-cells,in
R193 T230 T231 aux To,investigate
R194 T231 T216 advcl investigate,are
R195 T232 T233 det the,importance
R196 T233 T231 dobj importance,investigate
R197 T234 T233 prep of,importance
R198 T235 T234 pobj protein,of
R199 T236 T237 compound kinase,D
R200 T237 T235 appos D,protein
R201 T238 T237 punct (,D
R202 T239 T237 appos PKD,D
R203 T240 T237 punct ),D
R204 T241 T231 dobj enzymes,investigate
R205 T242 T243 nsubj we,generated
R206 T243 T241 relcl generated,enzymes
R207 T244 T249 det a,line
R208 T245 T249 compound PKD-null,line
R209 T246 T247 compound DT40,B-lymphocyte
R210 T247 T249 compound B-lymphocyte,line
R211 T248 T249 compound cell,line
R212 T249 T243 dobj line,generated
R213 T250 T216 punct .,are
R214 T251 T254 advmod Previously,shown
R215 T252 T254 nsubj we,shown
R216 T253 T254 aux have,shown
R217 T254 T254 ROOT shown,shown
R218 T255 T257 mark that,have
R219 T256 T257 nsubj PKDs,have
R220 T257 T254 ccomp have,shown
R221 T258 T260 det an,role
R222 T259 T260 amod essential,role
R223 T260 T257 dobj role,have
R224 T261 T260 prep in,role
R225 T262 T261 pcomp regulating,in
R226 T263 T266 compound class,deacetylases
R227 T264 T266 compound II,deacetylases
R2279 T2730 T2731 nummod "Protein kinase D enzymes are dispensable for proliferation, survival and antigen receptor-regulated NFκB activity in vertebrate B-cells Abstract To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. Most cell types express at least two PKD isoforms but PKD enzymes are especially highly expressed in haematopoietic cells, where they are activated in response to antigen receptors stimulation [2,3]. A conserved signalling pathway linking antigen receptors to PKDs involves the activation of PLCγ and the subsequent production of diacylglycerol (DAG) which stimulates classical and/or novel protein kinase Cs (PKC) that phosphorylate two key regulatory serine residues in the activation loop of PKD kinases [3–6]. The N-terminal regulatory region of PKD enzymes contains a DAG binding domain and direct binding of DAG also contributes to PKD1 activation [7] as well as regulating the spatial location of PKD enzymes within cells [8–12]. PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). In particular, PKDs have been widely linked to the activation of the NFκB transcription factor and in regulating cell survival during oxidative stress [17,21–23]. Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. An essential role for PKD enzymes in regulating class II histone deacetylases (HDACs), enzymes that repress MEF2-dependent gene transcription, has also been demonstrated [1,26–28]. To investigate the biological role of PKDs we have generated DT40 B cell lines that lack expression of one or more members of the PKD family [1], allowing us to investigate the function(s) of PKD isoforms following B cell antigen receptor (BCR) stimulation, as well addressing the issue of functional redundancy between the different PKD family members. Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. However, PKD-null DT40 B cells are viable and proliferate normally. Moreover, loss of the entire cellular pool of PKD does not critically affect oxidative stress responses in B cells nor do PKD kinases play an essential role in regulating NFκB transcriptional activity. Together, these findings reveal that in B lymphocytes, PKD kinases are not critical regulators of many of the cellular processes previously ascribed to them in other cellular systems. 2 Materials and methods 2.1 Cell culture, transient transfections and cell stimulation The generation, culture and activation of PKD1−/−, PKD3−/− and PKD1/3−/− knockout DT40 B cell lines have been described previously [1]. Cells were lysed and protein extracts were analysed in Western blotting experiments as previously described [1]. Chloramphenicol acetyl transferase assays have been described previously [29]. 2.2 sIgM staining DT40 B cells (2 × 106 cells per point) were resuspended in 200 μl buffer (RPMI 1640 media, 1% foetal calf serum) containing anti-chicken M1 monoclonal antibody conjugated to FITC for 20 min on ice. The cells were washed twice and fluorescent intensity was analysed by flow cytometry. All results shown are representative of at two to four independent experiments unless otherwise indicated. 3 Results 3.1 ",Loss
R228 T265 T266 compound histone,deacetylases
R2280 T2731 T2744 nsubj Loss,kinases
R2281 T2732 T2731 prep of,Loss
R2282 T2733 T2734 compound HSP27,phosphorylation
R2283 T2734 T2732 pobj phosphorylation,of
R2284 T2735 T2731 prep in,Loss
R2285 T2736 T2737 compound DT40,B
R2286 T2737 T2738 compound B,cells
R2287 T2738 T2735 pobj cells,in
R2288 T2739 T2744 advcl lacking,kinases
R2289 T2740 T2739 dobj expression,lacking
R229 T266 T262 dobj deacetylases,regulating
R2290 T2741 T2740 prep of,expression
R2291 T2742 T2743 compound PKD,family
R2292 T2743 T2741 pobj family,of
R2293 T2744 T2744 ROOT kinases,kinases
R2294 T2745 T2746 compound DT40,B
R2295 T2746 T2747 compound B,cells
R2296 T2747 T2748 nsubj cells,express
R2297 T2748 T2744 ccomp express,kinases
R2298 T2749 T2751 nummod two,isoforms
R2299 T2750 T2751 compound PKD,isoforms
R230 T267 T262 prep in,regulating
R2300 T2751 T2748 dobj isoforms,express
R2301 T2752 T2751 punct ",",isoforms
R2302 T2753 T2751 conj PKD1,isoforms
R2303 T2754 T2753 cc and,PKD1
R2304 T2755 T2753 conj PKD3,PKD1
R2305 T2756 T2755 punct ",",PKD3
R2306 T2757 T2748 cc and,express
R2307 T2758 T2760 mark as,described
R2308 T2759 T2760 advmod previously,described
R2309 T2760 T2764 advcl described,generated
R231 T268 T271 compound DT40,Matthews
R2310 T2761 T2764 nsubj we,generated
R2311 T2762 T2764 aux have,generated
R2312 T2763 T2764 advmod recently,generated
R2313 T2764 T2748 conj generated,express
R2314 T2765 T2768 compound DT40,lines
R2315 T2766 T2768 compound B,lines
R2316 T2767 T2768 compound cell,lines
R2317 T2768 T2764 dobj lines,generated
R2318 T2769 T2770 nsubj that,lack
R2319 T2770 T2768 relcl lack,lines
R232 T269 T271 compound B-cells,Matthews
R2320 T2771 T2770 dobj expression,lack
R2321 T2772 T2771 prep of,expression
R2322 T2773 T2774 det either,PKD1
R2323 T2774 T2772 pobj PKD1,of
R2324 T2775 T2774 cc or,PKD1
R2325 T2776 T2774 conj PKD3,PKD1
R2326 T2777 T2776 cc or,PKD3
R2327 T2778 T2779 det both,enzymes
R2328 T2779 T2772 pobj enzymes,of
R2329 T2780 T2782 nmod [,]
R233 T270 T271 compound [,Matthews
R2330 T2781 T2782 nummod 1,]
R2331 T2782 T2764 npadvmod ],generated
R2332 T2783 T2744 punct .,kinases
R2333 T2784 T2800 prep In,/
R2334 T2785 T2784 pcomp generating,In
R2335 T2786 T2790 det the,lines
R2336 T2787 T2789 amod double,cell
R2337 T2788 T2789 compound knockout,cell
R2338 T2789 T2790 compound cell,lines
R2339 T2790 T2785 dobj lines,generating
R234 T271 T267 pobj Matthews,in
R2340 T2791 T2792 nsubj we,targeted
R2341 T2792 T2790 relcl targeted,lines
R2342 T2793 T2795 det the,loci
R2343 T2794 T2795 compound PKD1,loci
R2344 T2795 T2792 dobj loci,targeted
R2345 T2796 T2792 prep in,targeted
R2346 T2797 T2799 det a,−
R2347 T2798 T2799 compound PKD3,−
R2348 T2799 T2796 pobj −,in
R2349 T2800 T2800 ROOT /,/
R235 T272 T271 punct ",",Matthews
R2350 T2801 T2803 nummod −,line
R2351 T2802 T2803 compound cell,line
R2352 T2803 T2800 dobj line,/
R2353 T2804 T2805 nsubj that,expressed
R2354 T2805 T2803 relcl expressed,line
R2355 T2806 T2808 det a,transgene
R2356 T2807 T2808 amod Flag-PKD3,transgene
R2357 T2808 T2805 dobj transgene,expressed
R2358 T2809 T2808 prep under,transgene
R2359 T2810 T2811 det the,control
R236 T273 T271 conj S.A.,Matthews
R2360 T2811 T2809 pobj control,under
R2361 T2812 T2811 prep of,control
R2362 T2813 T2815 det a,promoter
R2363 T2814 T2815 amod doxycycline-inducible,promoter
R2364 T2815 T2812 pobj promoter,of
R2365 T2816 T2800 punct .,/
R2366 T2817 T2832 advmod Hence,is
R2367 T2818 T2832 punct ",",is
R2368 T2819 T2826 nmod in,expression
R2369 T2820 T2821 det the,presence
R237 T274 T271 punct ",",Matthews
R2370 T2821 T2819 pobj presence,in
R2371 T2822 T2821 prep of,presence
R2372 T2823 T2822 pobj doxycycline,of
R2373 T2824 T2821 punct ",",presence
R2374 T2825 T2826 compound Flag-PKD3,expression
R2375 T2826 T2832 nsubj expression,is
R2376 T2827 T2826 prep in,expression
R2377 T2828 T2831 nummod PKD1/3,cells
R2378 T2829 T2831 amod double,cells
R2379 T2830 T2831 compound knockout,cells
R238 T275 T271 conj Liu,Matthews
R2380 T2831 T2827 pobj cells,in
R2381 T2832 T2832 ROOT is,is
R2382 T2833 T2832 acomp comparable,is
R2383 T2834 T2833 prep to,comparable
R2384 T2835 T2837 amod endogenous,present
R2385 T2836 T2837 amod PKD3,present
R2386 T2837 T2834 pobj present,to
R2387 T2838 T2837 prep in,present
R2388 T2839 T2841 amod wild-type,cells
R2389 T2840 T2841 compound DT40,cells
R239 T276 T275 punct ",",Liu
R2390 T2841 T2838 pobj cells,in
R2391 T2842 T2837 cc and,present
R2392 T2843 T2837 conj removal,present
R2393 T2844 T2843 prep of,removal
R2394 T2845 T2844 pobj doxycycline,of
R2395 T2846 T2843 prep from,removal
R2396 T2847 T2849 det the,media
R2397 T2848 T2849 compound culture,media
R2398 T2849 T2846 pobj media,from
R2399 T2850 T2832 prep for,is
R240 T277 T275 conj P.,Liu
R2400 T2851 T2852 nummod 5,days
R2401 T2852 T2853 compound days,results
R2402 T2853 T2850 pobj results,for
R2403 T2854 T2853 prep in,results
R2404 T2855 T2859 det a,phenotype
R2405 T2856 T2857 advmod completely,null
R2406 T2857 T2859 amod null,phenotype
R2407 T2858 T2859 compound PKD,phenotype
R2408 T2859 T2854 pobj phenotype,in
R2409 T2860 T2862 punct (,1A
R241 T278 T277 punct ",",P.
R2410 T2861 T2862 compound Fig.,1A
R2411 T2862 T2859 appos 1A,phenotype
R2412 T2863 T2862 punct ),1A
R2413 T2864 T2832 punct .,is
R2414 T2865 T2869 advmod Previously,demonstrated
R2415 T2866 T2869 punct ",",demonstrated
R2416 T2867 T2869 nsubj we,demonstrated
R2417 T2868 T2869 aux have,demonstrated
R2418 T2869 T2869 ROOT demonstrated,demonstrated
R2419 T2870 T2886 mark that,is
R242 T279 T277 conj Spitaler,P.
R2420 T2871 T2886 nsubj phosphorylation,is
R2421 T2872 T2871 cc and,phosphorylation
R2422 T2873 T2874 amod nuclear,exclusion
R2423 T2874 T2871 conj exclusion,phosphorylation
R2424 T2875 T2874 prep of,exclusion
R2425 T2876 T2879 nmod class,deacetylases
R2426 T2877 T2879 nmod II,deacetylases
R2427 T2878 T2879 compound histone,deacetylases
R2428 T2879 T2875 pobj deacetylases,of
R2429 T2880 T2879 punct (,deacetylases
R243 T280 T279 punct ",",Spitaler
R2430 T2881 T2879 appos HDACs,deacetylases
R2431 T2882 T2879 punct ),deacetylases
R2432 T2883 T2871 prep during,phosphorylation
R2433 T2884 T2885 compound BCR,engagement
R2434 T2885 T2883 pobj engagement,during
R2435 T2886 T2869 ccomp is,demonstrated
R2436 T2887 T2886 acomp defective,is
R2437 T2888 T2886 prep in,is
R2438 T2889 T2894 nummod PKD1/3,cells
R2439 T2890 T2894 nummod −,cells
R244 T281 T279 conj M.,Spitaler
R2440 T2891 T2894 nmod /,cells
R2441 T2892 T2894 compound −,cells
R2442 T2893 T2894 compound B,cells
R2443 T2894 T2888 pobj cells,in
R2444 T2895 T2886 cc and,is
R2445 T2896 T2897 aux can,restored
R2446 T2897 T2886 conj restored,is
R2447 T2898 T2897 prep upon,restored
R2448 T2899 T2898 pobj re-expression,upon
R2449 T2900 T2899 prep of,re-expression
R245 T282 T281 punct ",",M.
R2450 T2901 T2904 det a,isoform
R2451 T2902 T2904 amod single,isoform
R2452 T2903 T2904 compound PKD,isoform
R2453 T2904 T2900 pobj isoform,of
R2454 T2905 T2907 nmod [,]
R2455 T2906 T2907 nummod 1,]
R2456 T2907 T2869 dobj ],demonstrated
R2457 T2908 T2869 punct .,demonstrated
R2458 T2909 T2913 det The,protein
R2459 T2910 T2913 amod small,protein
R246 T283 T281 conj Olson,M.
R2460 T2911 T2912 compound heat,shock
R2461 T2912 T2913 compound shock,protein
R2462 T2913 T2918 nsubj protein,proposed
R2463 T2914 T2913 appos HSP27,protein
R2464 T2915 T2918 aux has,proposed
R2465 T2916 T2918 advmod recently,proposed
R2466 T2917 T2918 auxpass been,proposed
R2467 T2918 T2918 ROOT proposed,proposed
R2468 T2919 T2918 prep as,proposed
R2469 T2920 T2922 det a,substrate
R247 T284 T283 punct ",",Olson
R2470 T2921 T2922 compound PKD1,substrate
R2471 T2922 T2919 pobj substrate,as
R2472 T2923 T2925 nmod [,]
R2473 T2924 T2925 nummod 24,]
R2474 T2925 T2922 dep ],substrate
R2475 T2926 T2922 cc and,substrate
R2476 T2927 T2929 nsubj we,assessed
R2477 T2928 T2929 advmod accordingly,assessed
R2478 T2929 T2922 conj assessed,substrate
R2479 T2930 T2934 mark whether,have
R248 T285 T283 conj E.N.,Olson
R2480 T2931 T2932 compound PKD-null,DT40
R2481 T2932 T2933 compound DT40,cells
R2482 T2933 T2934 nsubj cells,have
R2483 T2934 T2929 ccomp have,assessed
R2484 T2935 T2936 amod defective,phosphorylation
R2485 T2936 T2934 dobj phosphorylation,have
R2486 T2937 T2936 prep of,phosphorylation
R2487 T2938 T2937 pobj HSP27,of
R2488 T2939 T2936 prep on,phosphorylation
R2489 T2940 T2939 pobj serine,on
R249 T286 T285 punct ",",E.N.
R2490 T2941 T2940 nummod 82,serine
R2491 T2942 T2936 punct ",",phosphorylation
R2492 T2943 T2947 det the,sequence
R2493 T2944 T2947 amod proposed,sequence
R2494 T2945 T2946 compound PKD1,substrate
R2495 T2946 T2947 compound substrate,sequence
R2496 T2947 T2936 appos sequence,phosphorylation
R2497 T2948 T2929 punct .,assessed
R2498 T2949 T2951 nsubj We,investigated
R2499 T2950 T2951 advmod initially,investigated
R250 T287 T285 conj McKinsey,E.N.
R2500 T2951 T2951 ROOT investigated,investigated
R2501 T2952 T2953 det the,regulation
R2502 T2953 T2951 dobj regulation,investigated
R2503 T2954 T2953 prep of,regulation
R2504 T2955 T2956 compound HSP27,phosphorylation
R2505 T2956 T2954 pobj phosphorylation,of
R2506 T2957 T2956 prep in,phosphorylation
R2507 T2958 T2959 amod single,knockout
R2508 T2959 T2962 compound knockout,cells
R2509 T2960 T2961 compound DT40,B
R251 T288 T287 punct ",",McKinsey
R2510 T2961 T2962 compound B,cells
R2511 T2962 T2957 pobj cells,in
R2512 T2963 T2951 advcl lacking,investigated
R2513 T2964 T2965 preconj either,PKD1
R2514 T2965 T2963 dobj PKD1,lacking
R2515 T2966 T2965 cc or,PKD1
R2516 T2967 T2965 conj PKD3,PKD1
R2517 T2968 T2951 punct .,investigated
R2518 T2969 T2970 mark As,shown
R2519 T2970 T2985 advcl shown,increased
R252 T289 T287 conj T.A.,McKinsey
R2520 T2971 T2970 prep in,shown
R2521 T2972 T2973 compound Fig.,1B
R2522 T2973 T2971 pobj 1B,in
R2523 T2974 T2973 punct ",",1B
R2524 T2975 T2973 appos activation,1B
R2525 T2976 T2975 prep of,activation
R2526 T2977 T2978 det the,BCR
R2527 T2978 T2976 pobj BCR,of
R2528 T2979 T2975 cc or,activation
R2529 T2980 T2975 conj treatment,activation
R253 T290 T287 punct ",",McKinsey
R2530 T2981 T2975 prep with,activation
R2531 T2982 T2984 det the,PdBu
R2532 T2983 T2984 compound DAG-mimetic,PdBu
R2533 T2984 T2981 pobj PdBu,with
R2534 T2985 T2985 ROOT increased,increased
R2535 T2986 T2987 det the,levels
R2536 T2987 T2985 dobj levels,increased
R2537 T2988 T2987 prep of,levels
R2538 T2989 T2990 compound HSP27,phosphorylation
R2539 T2990 T2988 pobj phosphorylation,of
R254 T291 T287 conj Cantrell,McKinsey
R2540 T2991 T2987 prep at,levels
R2541 T2992 T2991 pobj S82,at
R2542 T2993 T2992 prep in,S82
R2543 T2994 T2997 amod wild-type,cells
R2544 T2995 T2996 compound DT40,B
R2545 T2996 T2997 compound B,cells
R2546 T2997 T2993 pobj cells,in
R2547 T2998 T2985 punct .,increased
R2548 T2999 T3004 nsubj BCR,were
R2549 T3000 T2999 cc and,BCR
R255 T292 T291 punct ",",Cantrell
R2550 T3001 T3003 amod phorbol,signals
R2551 T3002 T3003 compound ester,signals
R2552 T3003 T2999 conj signals,BCR
R2553 T3004 T3004 ROOT were,were
R2554 T3005 T3004 advmod also,were
R2555 T3006 T3004 acomp able,were
R2556 T3007 T3008 aux to,increase
R2557 T3008 T3006 xcomp increase,able
R2558 T3009 T3010 compound HSP27,phosphorylation
R2559 T3010 T3008 dobj phosphorylation,increase
R256 T293 T291 conj D.A.,Cantrell
R2560 T3011 T3008 prep in,increase
R2561 T3012 T3016 nummod PKD1,knockout
R2562 T3013 T3012 cc or,PKD1
R2563 T3014 T3012 conj PKD3,PKD1
R2564 T3015 T3016 amod single,knockout
R2565 T3016 T3019 compound knockout,cells
R2566 T3017 T3018 compound DT40,B
R2567 T3018 T3019 compound B,cells
R2568 T3019 T3011 pobj cells,in
R2569 T3020 T3004 punct (,were
R257 T294 T293 cc and,D.A.
R2570 T3021 T3022 compound Fig.,1B
R2571 T3022 T3004 npadvmod 1B,were
R2572 T3023 T3004 punct ),were
R2573 T3024 T3004 punct .,were
R2574 T3025 T3038 advmod However,abolished
R2575 T3026 T3038 punct ",",abolished
R2576 T3027 T3038 nsubjpass BCR,abolished
R2577 T3028 T3027 punct -,BCR
R2578 T3029 T3027 cc and,BCR
R2579 T3030 T3032 nmod phorbol,phosphorylation
R258 T295 T293 conj Scharenberg,D.A.
R2580 T3031 T3032 amod ester-induced,phosphorylation
R2581 T3032 T3027 conj phosphorylation,BCR
R2582 T3033 T3032 prep of,phosphorylation
R2583 T3034 T3033 pobj HSP27,of
R2584 T3035 T3032 prep on,phosphorylation
R2585 T3036 T3035 pobj S82,on
R2586 T3037 T3038 auxpass was,abolished
R2587 T3038 T3038 ROOT abolished,abolished
R2588 T3039 T3038 prep in,abolished
R2589 T3040 T3041 compound B,cells
R259 T296 T295 punct ",",Scharenberg
R2590 T3041 T3039 pobj cells,in
R2591 T3042 T3043 nsubj that,lacked
R2592 T3043 T3041 relcl lacked,cells
R2593 T3044 T3045 preconj both,PKD1
R2594 T3045 T3043 dobj PKD1,lacked
R2595 T3046 T3045 cc and,PKD1
R2596 T3047 T3045 conj PKD3,PKD1
R2597 T3048 T3047 punct (,PKD3
R2598 T3049 T3050 compound Fig.,1C
R2599 T3050 T3047 appos 1C,PKD3
R260 T297 T295 conj A.M.,Scharenberg
R2600 T3051 T3047 punct ),PKD3
R2601 T3052 T3038 punct .,abolished
R2602 T3053 T3066 advmod Significantly,was
R2603 T3054 T3056 punct ",",expression
R2604 T3055 T3056 amod doxycycline-induced,expression
R2605 T3056 T3066 nsubj expression,was
R2606 T3057 T3056 prep of,expression
R2607 T3058 T3060 det the,transgene
R2608 T3059 T3060 compound Flag-PKD3,transgene
R2609 T3060 T3057 pobj transgene,of
R261 T298 T297 punct (,A.M.
R2610 T3061 T3060 prep in,transgene
R2611 T3062 T3065 det the,cells
R2612 T3063 T3065 amod double,cells
R2613 T3064 T3065 compound knockout,cells
R2614 T3065 T3061 pobj cells,in
R2615 T3066 T3066 ROOT was,was
R2616 T3067 T3066 acomp sufficient,was
R2617 T3068 T3069 aux to,restore
R2618 T3069 T3067 xcomp restore,sufficient
R2619 T3070 T3071 amod normal,regulation
R262 T299 T297 appos 2006,A.M.
R2620 T3071 T3069 dobj regulation,restore
R2621 T3072 T3071 prep of,regulation
R2622 T3073 T3074 compound HSP27,phosphorylation
R2623 T3074 T3072 pobj phosphorylation,of
R2624 T3075 T3077 punct (,1C
R2625 T3076 T3077 compound Fig.,1C
R2626 T3077 T3074 appos 1C,phosphorylation
R2627 T3078 T3077 punct ),1C
R2628 T3079 T3066 punct .,was
R2629 T3080 T3095 prep In,was
R263 T300 T297 punct ),A.M.
R2630 T3081 T3080 pobj contrast,In
R2631 T3082 T3095 punct ",",was
R2632 T3083 T3095 nsubj expression,was
R2633 T3084 T3083 prep of,expression
R2634 T3085 T3089 det a,protein
R2635 T3086 T3089 amod kinase-deficient,protein
R2636 T3087 T3089 amod PKD3,protein
R2637 T3088 T3089 amod mutant,protein
R2638 T3089 T3084 pobj protein,of
R2639 T3090 T3089 prep in,protein
R264 T301 T302 amod Essential,role
R2640 T3091 T3094 det the,cells
R2641 T3092 T3094 amod double,cells
R2642 T3093 T3094 compound knockout,cells
R2643 T3094 T3090 pobj cells,in
R2644 T3095 T3095 ROOT was,was
R2645 T3096 T3095 neg not,was
R2646 T3097 T3095 acomp able,was
R2647 T3098 T3099 aux to,restore
R2648 T3099 T3097 xcomp restore,able
R2649 T3100 T3099 dobj BCR,restore
R265 T302 T260 appos role,role
R2650 T3101 T3100 punct -,BCR
R2651 T3102 T3099 cc or,restore
R2652 T3103 T3099 conj phorbol,restore
R2653 T3104 T3106 amod ester-induced,phosphorylation
R2654 T3105 T3106 compound HSP27,phosphorylation
R2655 T3106 T3103 dobj phosphorylation,phorbol
R2656 T3107 T3106 punct (,phosphorylation
R2657 T3108 T3109 compound Fig.,1D
R2658 T3109 T3106 appos 1D,phosphorylation
R2659 T3110 T3106 punct ),phosphorylation
R266 T303 T302 prep for,role
R2660 T3111 T3095 punct .,was
R2661 T3112 T3120 advmod Hence,regulate
R2662 T3113 T3120 punct ",",regulate
R2663 T3114 T3120 nsubj PKD3,regulate
R2664 T3115 T3117 advmod as,as
R2665 T3116 T3117 advmod well,as
R2666 T3117 T3114 cc as,PKD3
R2667 T3118 T3114 conj PKD1,PKD3
R2668 T3119 T3120 aux can,regulate
R2669 T3120 T3120 ROOT regulate,regulate
R267 T304 T303 pobj protein,for
R2670 T3121 T3122 compound HSP27,phosphorylation
R2671 T3122 T3120 dobj phosphorylation,regulate
R2672 T3123 T3120 cc and,regulate
R2673 T3124 T3120 prep in,regulate
R2674 T3125 T3126 compound DT40,B
R2675 T3126 T3127 compound B,cells
R2676 T3127 T3124 pobj cells,in
R2677 T3128 T3129 nsubj they,are
R2678 T3129 T3120 conj are,regulate
R2679 T3130 T3131 advmod functionally,redundant
R268 T305 T308 compound kinase,kinases
R2680 T3131 T3129 acomp redundant,are
R2681 T3132 T3131 prep as,redundant
R2682 T3133 T3134 compound HSP27,kinases
R2683 T3134 T3132 pobj kinases,as
R2684 T3135 T3129 punct .,are
R269 T306 T307 compound D,family
R270 T307 T308 compound family,kinases
R271 T308 T302 conj kinases,role
R272 T309 T308 prep in,kinases
R273 T310 T311 det the,regulation
R274 T311 T309 pobj regulation,in
R275 T312 T311 prep of,regulation
R276 T313 T316 compound class,deacetylases
R277 T314 T316 compound II,deacetylases
R278 T315 T316 compound histone,deacetylases
R279 T316 T312 pobj deacetylases,of
R280 T317 T316 prep in,deacetylases
R281 T318 T319 compound B,lymphocytes
R282 T319 T317 pobj lymphocytes,in
R283 T320 T254 punct .,shown
R284 T321 T321 ROOT Mol,Mol
R285 T322 T321 punct .,Mol
R286 T323 T324 compound Cell,Biol
R287 T324 T324 ROOT Biol,Biol
R288 T325 T326 punct .,26
R289 T326 T324 nummod 26,Biol
R290 T327 T324 punct ",",Biol
R291 T328 T324 appos 1569,Biol
R292 T329 T324 appos 1577,Biol
R293 T330 T330 ROOT ],]
R294 T331 T324 punct .,Biol
R295 T332 T334 nsubj We,show
R296 T333 T334 advmod now,show
R297 T334 T334 ROOT show,show
R298 T335 T339 mark that,required
R299 T336 T339 nsubjpass PKDs,required
R300 T337 T339 auxpass are,required
R301 T338 T339 advmod also,required
R302 T339 T334 ccomp required,show
R303 T340 T341 aux to,regulate
R304 T341 T339 xcomp regulate,required
R305 T342 T343 compound HSP27,phosphorylation
R306 T343 T341 dobj phosphorylation,regulate
R307 T344 T343 prep in,phosphorylation
R308 T345 T346 compound DT40,B-cells
R309 T346 T344 pobj B-cells,in
R310 T347 T334 punct .,show
R311 T348 T364 advmod However,regulate
R312 T349 T364 punct ",",regulate
R313 T350 T364 prep in,regulate
R314 T351 T350 pobj contrast,in
R315 T352 T351 prep to,contrast
R316 T353 T354 amod previous,observations
R317 T354 T352 pobj observations,to
R318 T355 T354 prep in,observations
R319 T356 T358 amod other,types
R320 T357 T358 compound cell,types
R321 T358 T355 pobj types,in
R322 T359 T364 punct ",",regulate
R323 T360 T364 nsubj PKD,regulate
R324 T361 T364 nsubj enzymes,regulate
R325 T362 T364 aux do,regulate
R326 T363 T364 neg not,regulate
R327 T364 T364 ROOT regulate,regulate
R328 T365 T367 amod basic,processes
R329 T366 T367 amod cellular,processes
R330 T367 T364 dobj processes,regulate
R331 T368 T369 amod such,as
R332 T369 T367 prep as,processes
R333 T370 T369 pobj proliferation,as
R334 T371 T370 cc or,proliferation
R335 T372 T370 conj survival,proliferation
R336 T373 T370 conj responses,proliferation
R337 T374 T373 punct ",",responses
R338 T375 T364 cc nor,regulate
R339 T376 T378 nmod NFκB,activity
R340 T377 T378 amod transcriptional,activity
R341 T378 T364 conj activity,regulate
R3416 T4217 T4219 nummod "Protein kinase D enzymes are dispensable for proliferation, survival and antigen receptor-regulated NFκB activity in vertebrate B-cells Abstract To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. Most cell types express at least two PKD isoforms but PKD enzymes are especially highly expressed in haematopoietic cells, where they are activated in response to antigen receptors stimulation [2,3]. A conserved signalling pathway linking antigen receptors to PKDs involves the activation of PLCγ and the subsequent production of diacylglycerol (DAG) which stimulates classical and/or novel protein kinase Cs (PKC) that phosphorylate two key regulatory serine residues in the activation loop of PKD kinases [3–6]. The N-terminal regulatory region of PKD enzymes contains a DAG binding domain and direct binding of DAG also contributes to PKD1 activation [7] as well as regulating the spatial location of PKD enzymes within cells [8–12]. PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). In particular, PKDs have been widely linked to the activation of the NFκB transcription factor and in regulating cell survival during oxidative stress [17,21–23]. Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. An essential role for PKD enzymes in regulating class II histone deacetylases (HDACs), enzymes that repress MEF2-dependent gene transcription, has also been demonstrated [1,26–28]. To investigate the biological role of PKDs we have generated DT40 B cell lines that lack expression of one or more members of the PKD family [1], allowing us to investigate the function(s) of PKD isoforms following B cell antigen receptor (BCR) stimulation, as well addressing the issue of functional redundancy between the different PKD family members. Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. However, PKD-null DT40 B cells are viable and proliferate normally. Moreover, loss of the entire cellular pool of PKD does not critically affect oxidative stress responses in B cells nor do PKD kinases play an essential role in regulating NFκB transcriptional activity. Together, these findings reveal that in B lymphocytes, PKD kinases are not critical regulators of many of the cellular processes previously ascribed to them in other cellular systems. 2 Materials and methods 2.1 Cell culture, transient transfections and cell stimulation The generation, culture and activation of PKD1−/−, PKD3−/− and PKD1/3−/− knockout DT40 B cell lines have been described previously [1]. Cells were lysed and protein extracts were analysed in Western blotting experiments as previously described [1]. Chloramphenicol acetyl transferase assays have been described previously [29]. 2.2 sIgM staining DT40 B cells (2 × 106 cells per point) were resuspended in 200 μl buffer (RPMI 1640 media, 1% foetal calf serum) containing anti-chicken M1 monoclonal antibody conjugated to FITC for 20 min on ice. The cells were washed twice and fluorescent intensity was analysed by flow cytometry. All results shown are representative of at two to four independent experiments unless otherwise indicated. 3 Results 3.1 Loss of HSP27 phosphorylation in DT40 B cells lacking expression of PKD family kinases DT40 B cells express two PKD isoforms, PKD1 and PKD3, and as previously described we have recently generated DT40 B cell lines that lack expression of either PKD1 or PKD3 or both enzymes [1]. In generating the double knockout cell lines we targeted the PKD1 loci in a PKD3−/− cell line that expressed a Flag-PKD3 transgene under the control of a doxycycline-inducible promoter. Hence, in the presence of doxycycline, Flag-PKD3 expression in PKD1/3 double knockout cells is comparable to endogenous PKD3 present in wild-type DT40 cells and removal of doxycycline from the culture media for 5 days results in a completely null PKD phenotype (Fig. 1A). Previously, we have demonstrated that phosphorylation and nuclear exclusion of class II histone deacetylases (HDACs) during BCR engagement is defective in PKD1/3−/− B cells and can restored upon re-expression of a single PKD isoform [1]. The small heat shock protein HSP27 has recently been proposed as a PKD1 substrate [24] and we accordingly assessed whether PKD-null DT40 cells have defective phosphorylation of HSP27 on serine 82, the proposed PKD1 substrate sequence. We initially investigated the regulation of HSP27 phosphorylation in single knockout DT40 B cells lacking either PKD1 or PKD3. As shown in Fig. 1B, activation of the BCR or treatment with the DAG-mimetic PdBu increased the levels of HSP27 phosphorylation at S82 in wild-type DT40 B cells. BCR and phorbol ester signals were also able to increase HSP27 phosphorylation in PKD1 or PKD3 single knockout DT40 B cells (Fig. 1B). However, BCR- and phorbol ester-induced phosphorylation of HSP27 on S82 was abolished in B cells that lacked both PKD1 and PKD3 (Fig. 1C). Significantly, doxycycline-induced expression of the Flag-PKD3 transgene in the double knockout cells was sufficient to restore normal regulation of HSP27 phosphorylation (Fig. 1C). In contrast, expression of a kinase-deficient PKD3 mutant protein in the double knockout cells was not able to restore BCR- or phorbol ester-induced HSP27 phosphorylation (Fig. 1D). Hence, PKD3 as well as PKD1 can regulate HSP27 phosphorylation and in DT40 B cells they are functionally redundant as HSP27 kinases. 3.2 ",proliferation
R3417 T4218 T4219 compound Cellular,proliferation
R3418 T4219 T4231 nsubj proliferation,kinases
R3419 T4220 T4219 cc and,proliferation
R342 T379 T378 amod downstream,activity
R3420 T4221 T4219 conj survival,proliferation
R3421 T4222 T4219 prep in,proliferation
R3422 T4223 T4224 compound DT40,B
R3423 T4224 T4225 compound B,cells
R3424 T4225 T4222 pobj cells,in
R3425 T4226 T4231 advcl lacking,kinases
R3426 T4227 T4226 dobj expression,lacking
R3427 T4228 T4227 prep of,expression
R3428 T4229 T4230 compound PKD,family
R3429 T4230 T4228 pobj family,of
R343 T380 T379 prep of,downstream
R3430 T4231 T4231 ROOT kinases,kinases
R3431 T4232 T4233 compound PKD,enzymes
R3432 T4233 T4237 nsubjpass enzymes,linked
R3433 T4234 T4237 aux have,linked
R3434 T4235 T4237 advmod previously,linked
R3435 T4236 T4237 auxpass been,linked
R3436 T4237 T4231 ccomp linked,kinases
R3437 T4238 T4237 prep to,linked
R3438 T4239 T4240 det the,regulation
R3439 T4240 T4238 pobj regulation,to
R344 T381 T385 det the,receptor
R3440 T4241 T4240 prep of,regulation
R3441 T4242 T4243 compound cell,proliferation
R3442 T4243 T4241 pobj proliferation,of
R3443 T4244 T4243 cc and,proliferation
R3444 T4245 T4243 conj survival,proliferation
R3445 T4246 T4243 punct (,proliferation
R3446 T4247 T4240 acl reviewed,regulation
R3447 T4248 T4247 prep in,reviewed
R3448 T4249 T4248 pobj [,in
R3449 T4250 T4251 nummod 20,]
R345 T382 T384 compound B,antigen
R3450 T4251 T4249 appos ],[
R3451 T4252 T4249 punct ),[
R3452 T4253 T4231 punct .,kinases
R3453 T4254 T4255 aux To,investigate
R3454 T4255 T4271 advcl investigate,cultured
R3455 T4256 T4257 det the,effect
R3456 T4257 T4255 dobj effect,investigate
R3457 T4258 T4263 dobj that,had
R3458 T4259 T4263 nsubj loss,had
R3459 T4260 T4259 prep of,loss
R346 T383 T384 compound cell,antigen
R3460 T4261 T4262 compound PKD,kinases
R3461 T4262 T4260 pobj kinases,of
R3462 T4263 T4257 relcl had,effect
R3463 T4264 T4263 prep on,had
R3464 T4265 T4267 compound B,survival
R3465 T4266 T4267 compound cell,survival
R3466 T4267 T4264 pobj survival,on
R3467 T4268 T4263 cc and/or,had
R3468 T4269 T4271 dobj proliferation,cultured
R3469 T4270 T4271 nsubj we,cultured
R347 T384 T385 compound antigen,receptor
R3470 T4271 T4271 ROOT cultured,cultured
R3471 T4272 T4275 amod wild-type,cells
R3472 T4273 T4272 cc and,wild-type
R3473 T4274 T4272 conj PKD-null,wild-type
R3474 T4275 T4271 dobj cells,cultured
R3475 T4276 T4271 prep in,cultured
R3476 T4277 T4278 det the,presence
R3477 T4278 T4276 pobj presence,in
R3478 T4279 T4278 punct (,presence
R3479 T4280 T4300 nsubj PKD1/3,monitored
R348 T385 T380 pobj receptor,of
R3480 T4281 T4283 nummod −,−
R3481 T4282 T4283 compound /,−
R3482 T4283 T4300 dep −,monitored
R3483 T4284 T4283 punct :,−
R3484 T4285 T4287 nmod Flag-PKD3,ve
R3485 T4286 T4287 compound +,ve
R3486 T4287 T4283 appos ve,−
R3487 T4288 T4287 punct ),ve
R3488 T4289 T4287 cc or,ve
R3489 T4290 T4287 conj absence,ve
R349 T386 T364 punct .,regulate
R3490 T4291 T4290 punct (,absence
R3491 T4292 T4295 nummod PKD1/3,−
R3492 T4293 T4295 nummod −,−
R3493 T4294 T4295 compound /,−
R3494 T4295 T4290 appos −,absence
R3495 T4296 T4295 punct ),−
R3496 T4297 T4290 prep of,absence
R3497 T4298 T4297 pobj doxycycline,of
R3498 T4299 T4290 cc and,absence
R3499 T4300 T4271 advcl monitored,cultured
R350 T387 T390 advmod Thus,have
R3500 T4301 T4302 amod exponential,growth
R3501 T4302 T4300 dobj growth,monitored
R3502 T4303 T4271 punct .,cultured
R3503 T4304 T4305 mark As,shown
R3504 T4305 T4311 advcl shown,−
R3505 T4306 T4305 prep in,shown
R3506 T4307 T4308 compound Fig.,2A
R3507 T4308 T4306 pobj 2A,in
R3508 T4309 T4311 punct ",",−
R3509 T4310 T4311 nsubj PKD1/3,−
R351 T388 T390 punct ",",have
R3510 T4311 T4311 ROOT −,−
R3511 T4312 T4314 nummod /,cells
R3512 T4313 T4314 compound −,cells
R3513 T4314 T4315 nsubj cells,proliferated
R3514 T4315 T4311 ccomp proliferated,−
R3515 T4316 T4315 advmod exponentially,proliferated
R3516 T4317 T4315 cc and,proliferated
R3517 T4318 T4324 nsubj re-expression,had
R3518 T4319 T4318 prep of,re-expression
R3519 T4320 T4319 pobj Flag-PKD3,of
R352 T389 T390 nsubj PKDs,have
R3520 T4321 T4318 prep in,re-expression
R3521 T4322 T4323 det these,cells
R3522 T4323 T4321 pobj cells,in
R3523 T4324 T4315 conj had,proliferated
R3524 T4325 T4326 det no,impact
R3525 T4326 T4324 dobj impact,had
R3526 T4327 T4326 prep on,impact
R3527 T4328 T4329 det the,rate
R3528 T4329 T4327 pobj rate,on
R3529 T4330 T4329 prep of,rate
R353 T390 T390 ROOT have,have
R3530 T4331 T4330 pobj proliferation,of
R3531 T4332 T4311 punct .,−
R3532 T4333 T4347 advmod Furthermore,was
R3533 T4334 T4347 punct ",",was
R3534 T4335 T4336 det the,viability
R3535 T4336 T4347 nsubj viability,was
R3536 T4337 T4336 prep of,viability
R3537 T4338 T4343 nummod PKD1/3,cells
R3538 T4339 T4343 nummod −,cells
R3539 T4340 T4343 compound /,cells
R354 T391 T393 det a,role
R3540 T4341 T4343 compound −,cells
R3541 T4342 T4343 compound B,cells
R3542 T4343 T4337 pobj cells,of
R3543 T4344 T4336 prep during,viability
R3544 T4345 T4346 amod routine,culturing
R3545 T4346 T4344 pobj culturing,during
R3546 T4347 T4347 ROOT was,was
R3547 T4348 T4347 neg not,was
R3548 T4349 T4350 advmod significantly,different
R3549 T4350 T4347 acomp different,was
R355 T392 T393 amod selective,role
R3550 T4351 T4350 prep from,different
R3551 T4352 T4351 pobj that,from
R3552 T4353 T4352 prep of,that
R3553 T4354 T4356 amod wild-type,cells
R3554 T4355 T4356 compound B,cells
R3555 T4356 T4353 pobj cells,of
R3556 T4357 T4360 punct (,shown
R3557 T4358 T4360 nsubjpass data,shown
R3558 T4359 T4360 neg not,shown
R3559 T4360 T4347 conj shown,was
R356 T393 T390 dobj role,have
R3560 T4361 T4360 punct ),shown
R3561 T4362 T4347 punct .,was
R3562 T4363 T4365 nsubjpass It,noted
R3563 T4364 T4365 auxpass was,noted
R3564 T4365 T4365 ROOT noted,noted
R3565 T4366 T4377 mark that,was
R3566 T4367 T4370 det the,time
R3567 T4368 T4369 compound population,doubling
R3568 T4369 T4370 amod doubling,time
R3569 T4370 T4377 nsubj time,was
R357 T394 T393 prep in,role
R3570 T4371 T4370 prep of,time
R3571 T4372 T4376 nummod PKD1/3,cells
R3572 T4373 T4376 nummod −,cells
R3573 T4374 T4376 compound /,cells
R3574 T4375 T4376 compound −,cells
R3575 T4376 T4371 pobj cells,of
R3576 T4377 T4365 ccomp was,noted
R3577 T4378 T4379 advmod slightly,slower
R3578 T4379 T4377 acomp slower,was
R3579 T4380 T4379 prep than,slower
R358 T395 T396 compound DT40,B-cell
R3580 T4381 T4380 pobj that,than
R3581 T4382 T4381 prep of,that
R3582 T4383 T4384 amod wild,type
R3583 T4384 T4382 pobj type,of
R3584 T4385 T4386 nummod DT40,cells
R3585 T4386 T4384 appos cells,type
R3586 T4387 T4386 punct (,cells
R3587 T4388 T4391 nummod 12.7,h
R3588 T4389 T4391 nmod ±,h
R3589 T4390 T4391 nummod 2.8,h
R359 T396 T397 compound B-cell,biology
R3590 T4391 T4386 appos h,cells
R3591 T4392 T4391 prep versus,h
R3592 T4393 T4396 nummod 10.2,h
R3593 T4394 T4396 nmod ±,h
R3594 T4395 T4396 nummod 0.4,h
R3595 T4396 T4392 pobj h,versus
R3596 T4397 T4386 punct ),cells
R3597 T4398 T4365 cc but,noted
R3598 T4399 T4400 det the,failure
R3599 T4400 T4415 nsubj failure,suggests
R360 T397 T394 pobj biology,in
R3600 T4401 T4400 prep of,failure
R3601 T4402 T4403 nummod PKD3,re-expression
R3602 T4403 T4401 pobj re-expression,of
R3603 T4404 T4405 aux to,modify
R3604 T4405 T4400 acl modify,failure
R3605 T4406 T4408 det the,rate
R3606 T4407 T4408 compound proliferation,rate
R3607 T4408 T4405 dobj rate,modify
R3608 T4409 T4408 prep of,rate
R3609 T4410 T4414 nummod PKD1/3,cells
R361 T398 T390 punct .,have
R3610 T4411 T4414 nummod −,cells
R3611 T4412 T4414 compound /,cells
R3612 T4413 T4414 compound −,cells
R3613 T4414 T4409 pobj cells,of
R3614 T4415 T4365 conj suggests,noted
R3615 T4416 T4420 mark that,were
R3616 T4417 T4419 det these,differences
R3617 T4418 T4419 amod small,differences
R3618 T4419 T4420 nsubj differences,were
R3619 T4420 T4415 ccomp were,suggests
R3620 T4421 T4422 advmod most,likely
R3621 T4422 T4420 acomp likely,were
R3622 T4423 T4424 det the,result
R3623 T4424 T4420 attr result,were
R3624 T4425 T4424 prep of,result
R3625 T4426 T4427 amod clonal,variation
R3626 T4427 T4425 pobj variation,of
R3627 T4428 T4420 cc and,were
R3628 T4429 T4431 auxpass were,caused
R3629 T4430 T4431 neg not,caused
R3630 T4431 T4420 conj caused,were
R3631 T4432 T4431 advmod specifically,caused
R3632 T4433 T4431 agent by,caused
R3633 T4434 T4433 pobj loss,by
R3634 T4435 T4434 prep of,loss
R3635 T4436 T4437 compound PKD,enzymes
R3636 T4437 T4435 pobj enzymes,of
R3637 T4438 T4415 punct .,suggests
R3638 T4439 T4444 advmod Thus,are
R3639 T4440 T4444 punct ",",are
R3640 T4441 T4443 compound PKD,enzymes
R3641 T4442 T4443 compound family,enzymes
R3642 T4443 T4444 nsubj enzymes,are
R3643 T4444 T4444 ROOT are,are
R3644 T4445 T4444 neg not,are
R3645 T4446 T4444 acomp essential,are
R3646 T4447 T4446 prep for,essential
R3647 T4448 T4447 pcomp regulating,for
R3648 T4449 T4450 amod basal,survival
R3649 T4450 T4448 dobj survival,regulating
R3650 T4451 T4450 cc and,survival
R3651 T4452 T4450 conj proliferation,survival
R3652 T4453 T4452 prep of,proliferation
R3653 T4454 T4455 compound DT40,B
R3654 T4455 T4456 compound B,cells
R3655 T4456 T4453 pobj cells,of
R3656 T4457 T4444 punct .,are
R3657 T4458 T4459 compound PKD,enzymes
R3658 T4459 T4469 nsubj enzymes,linked
R3659 T4460 T4459 punct ",",enzymes
R3660 T4461 T4462 advmod specifically,PKD1
R3661 T4462 T4459 appos PKD1,enzymes
R3662 T4463 T4462 cc and,PKD1
R3663 T4464 T4462 conj PKD2,PKD1
R3664 T4465 T4469 punct ",",linked
R3665 T4466 T4469 aux have,linked
R3666 T4467 T4469 advmod previously,linked
R3667 T4468 T4469 auxpass been,linked
R3668 T4469 T4469 ROOT linked,linked
R3669 T4470 T4469 prep to,linked
R3670 T4471 T4473 det a,role
R3671 T4472 T4473 amod protective,role
R3672 T4473 T4470 pobj role,to
R3673 T4474 T4473 prep against,role
R3674 T4475 T4477 amod oxidative,injury
R3675 T4476 T4477 amod stress-induced,injury
R3676 T4477 T4486 nmod injury,lines
R3677 T4478 T4477 prep in,injury
R3678 T4479 T4480 compound 3T3,fibroblast
R3679 T4480 T4478 pobj fibroblast,in
R3680 T4481 T4480 punct ",",fibroblast
R3681 T4482 T4480 conj HeLa,fibroblast
R3682 T4483 T4482 cc and,HeLa
R3683 T4484 T4486 amod epithelial,lines
R3684 T4485 T4486 compound cell,lines
R3685 T4486 T4474 pobj lines,against
R3686 T4487 T4488 compound [,"17,30"
R3687 T4488 T4486 appos "17,30",lines
R3688 T4489 T4490 nummod 32,]
R3689 T4490 T4486 appos ],lines
R3690 T4491 T4469 punct .,linked
R3691 T4492 T4494 nsubj We,addressed
R3692 T4493 T4494 advmod therefore,addressed
R3693 T4494 T4494 ROOT addressed,addressed
R3694 T4495 T4496 det the,role
R3695 T4496 T4494 dobj role,addressed
R3696 T4497 T4496 prep of,role
R3697 T4498 T4499 compound PKD,family
R3698 T4499 T4500 compound family,kinases
R3699 T4500 T4497 pobj kinases,of
R3700 T4501 T4496 prep in,role
R3701 T4502 T4501 pcomp regulating,in
R3702 T4503 T4504 compound B,cell
R3703 T4504 T4505 compound cell,survival
R3704 T4505 T4502 dobj survival,regulating
R3705 T4506 T4502 prep in,regulating
R3706 T4507 T4506 pobj response,in
R3707 T4508 T4507 prep to,response
R3708 T4509 T4510 amod oxidative,stress
R3709 T4510 T4508 pobj stress,to
R3710 T4511 T4510 cc and,stress
R3711 T4512 T4514 amod other,stimuli
R3712 T4513 T4514 compound stress,stimuli
R3713 T4514 T4510 conj stimuli,stress
R3714 T4515 T4494 punct .,addressed
R3715 T4516 T4517 mark As,shown
R3716 T4517 T4526 advcl shown,had
R3717 T4518 T4517 prep in,shown
R3718 T4519 T4520 compound Fig.,2B
R3719 T4520 T4518 pobj 2B,in
R3720 T4521 T4520 punct ",",2B
R3721 T4522 T4520 appos loss,2B
R3722 T4523 T4522 prep of,loss
R3723 T4524 T4525 nummod PKD1/3,expression
R3724 T4525 T4523 pobj expression,of
R3725 T4526 T4526 ROOT had,had
R3726 T4527 T4529 det no,impact
R3727 T4528 T4529 amod significant,impact
R3728 T4529 T4526 dobj impact,had
R3729 T4530 T4529 prep on,impact
R3730 T4531 T4532 det the,survival
R3731 T4532 T4530 pobj survival,on
R3732 T4533 T4532 prep of,survival
R3733 T4534 T4535 compound DT40,B
R3734 T4535 T4536 compound B,cells
R3735 T4536 T4533 pobj cells,of
R3736 T4537 T4526 prep in,had
R3737 T4538 T4537 pobj response,in
R3738 T4539 T4538 prep to,response
R3739 T4540 T4542 amod mitochondrial,stimuli
R3740 T4541 T4542 compound stress,stimuli
R3741 T4542 T4539 pobj stimuli,to
R3742 T4543 T4542 punct (,stimuli
R3743 T4544 T4542 appos H2O2,stimuli
R3744 T4545 T4544 cc or,H2O2
R3745 T4546 T4547 compound serum,deprivation
R3746 T4547 T4544 conj deprivation,H2O2
R3747 T4548 T4542 punct ),stimuli
R3748 T4549 T4542 punct ;,stimuli
R3749 T4550 T4552 amod DNA,agents
R3750 T4551 T4552 amod damaging,agents
R3751 T4552 T4542 conj agents,stimuli
R3752 T4553 T4552 punct (,agents
R3753 T4554 T4552 appos etoposide,agents
R3754 T4555 T4554 cc or,etoposide
R3755 T4556 T4554 conj doxorubicin,etoposide
R3756 T4557 T4552 punct ),agents
R3757 T4558 T4526 punct ;,had
R3758 T4559 T4561 compound ER,stress
R3759 T4560 T4561 compound pathway,stress
R3760 T4561 T4570 nsubj stress,following
R3761 T4562 T4561 amod due,stress
R3762 T4563 T4562 pcomp to,due
R3763 T4564 T4565 compound calcium,overload
R3764 T4565 T4562 pobj overload,due
R3765 T4566 T4567 punct (,thapsigargin
R3766 T4567 T4565 appos thapsigargin,overload
R3767 T4568 T4567 punct ),thapsigargin
R3768 T4569 T4565 cc or,overload
R3769 T4570 T4526 advcl following,had
R3770 T4571 T4572 amod prolonged,treatment
R3771 T4572 T4570 dobj treatment,following
R3772 T4573 T4572 prep with,treatment
R3773 T4574 T4575 compound phorbol,esters
R3774 T4575 T4573 pobj esters,with
R3775 T4576 T4575 cc or,esters
R3776 T4577 T4578 compound Trichostatin,A
R3777 T4578 T4575 conj A,esters
R3778 T4579 T4578 punct ",",A
R3779 T4580 T4581 det an,inhibitor
R3780 T4581 T4578 appos inhibitor,A
R3781 T4582 T4581 prep of,inhibitor
R3782 T4583 T4585 compound class,HDACs
R3783 T4584 T4585 compound I/II,HDACs
R3784 T4585 T4582 pobj HDACs,of
R3785 T4586 T4526 punct .,had
R3786 T4587 T4593 advmod Thus,play
R3787 T4588 T4593 punct ",",play
R3788 T4589 T4590 compound PKD,kinases
R3789 T4590 T4593 nsubj kinases,play
R3790 T4591 T4593 aux do,play
R3791 T4592 T4593 neg not,play
R3792 T4593 T4593 ROOT play,play
R3793 T4594 T4596 det an,role
R3794 T4595 T4596 amod essential,role
R3795 T4596 T4593 dobj role,play
R3796 T4597 T4593 prep in,play
R3797 T4598 T4597 pcomp regulating,in
R3798 T4599 T4600 compound B,cell
R3799 T4600 T4601 compound cell,survival
R3800 T4601 T4598 dobj survival,regulating
R3801 T4602 T4598 prep in,regulating
R3802 T4603 T4602 pobj response,in
R3803 T4604 T4603 prep to,response
R3804 T4605 T4606 det a,range
R3805 T4606 T4604 pobj range,to
R3806 T4607 T4606 prep of,range
R3807 T4608 T4610 amod different,stimuli
R3808 T4609 T4610 compound stress,stimuli
R3809 T4610 T4607 pobj stimuli,of
R3810 T4611 T4593 punct .,play
R4621 T5768 T5770 nummod "Protein kinase D enzymes are dispensable for proliferation, survival and antigen receptor-regulated NFκB activity in vertebrate B-cells Abstract To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. Most cell types express at least two PKD isoforms but PKD enzymes are especially highly expressed in haematopoietic cells, where they are activated in response to antigen receptors stimulation [2,3]. A conserved signalling pathway linking antigen receptors to PKDs involves the activation of PLCγ and the subsequent production of diacylglycerol (DAG) which stimulates classical and/or novel protein kinase Cs (PKC) that phosphorylate two key regulatory serine residues in the activation loop of PKD kinases [3–6]. The N-terminal regulatory region of PKD enzymes contains a DAG binding domain and direct binding of DAG also contributes to PKD1 activation [7] as well as regulating the spatial location of PKD enzymes within cells [8–12]. PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). In particular, PKDs have been widely linked to the activation of the NFκB transcription factor and in regulating cell survival during oxidative stress [17,21–23]. Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. An essential role for PKD enzymes in regulating class II histone deacetylases (HDACs), enzymes that repress MEF2-dependent gene transcription, has also been demonstrated [1,26–28]. To investigate the biological role of PKDs we have generated DT40 B cell lines that lack expression of one or more members of the PKD family [1], allowing us to investigate the function(s) of PKD isoforms following B cell antigen receptor (BCR) stimulation, as well addressing the issue of functional redundancy between the different PKD family members. Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. However, PKD-null DT40 B cells are viable and proliferate normally. Moreover, loss of the entire cellular pool of PKD does not critically affect oxidative stress responses in B cells nor do PKD kinases play an essential role in regulating NFκB transcriptional activity. Together, these findings reveal that in B lymphocytes, PKD kinases are not critical regulators of many of the cellular processes previously ascribed to them in other cellular systems. 2 Materials and methods 2.1 Cell culture, transient transfections and cell stimulation The generation, culture and activation of PKD1−/−, PKD3−/− and PKD1/3−/− knockout DT40 B cell lines have been described previously [1]. Cells were lysed and protein extracts were analysed in Western blotting experiments as previously described [1]. Chloramphenicol acetyl transferase assays have been described previously [29]. 2.2 sIgM staining DT40 B cells (2 × 106 cells per point) were resuspended in 200 μl buffer (RPMI 1640 media, 1% foetal calf serum) containing anti-chicken M1 monoclonal antibody conjugated to FITC for 20 min on ice. The cells were washed twice and fluorescent intensity was analysed by flow cytometry. All results shown are representative of at two to four independent experiments unless otherwise indicated. 3 Results 3.1 Loss of HSP27 phosphorylation in DT40 B cells lacking expression of PKD family kinases DT40 B cells express two PKD isoforms, PKD1 and PKD3, and as previously described we have recently generated DT40 B cell lines that lack expression of either PKD1 or PKD3 or both enzymes [1]. In generating the double knockout cell lines we targeted the PKD1 loci in a PKD3−/− cell line that expressed a Flag-PKD3 transgene under the control of a doxycycline-inducible promoter. Hence, in the presence of doxycycline, Flag-PKD3 expression in PKD1/3 double knockout cells is comparable to endogenous PKD3 present in wild-type DT40 cells and removal of doxycycline from the culture media for 5 days results in a completely null PKD phenotype (Fig. 1A). Previously, we have demonstrated that phosphorylation and nuclear exclusion of class II histone deacetylases (HDACs) during BCR engagement is defective in PKD1/3−/− B cells and can restored upon re-expression of a single PKD isoform [1]. The small heat shock protein HSP27 has recently been proposed as a PKD1 substrate [24] and we accordingly assessed whether PKD-null DT40 cells have defective phosphorylation of HSP27 on serine 82, the proposed PKD1 substrate sequence. We initially investigated the regulation of HSP27 phosphorylation in single knockout DT40 B cells lacking either PKD1 or PKD3. As shown in Fig. 1B, activation of the BCR or treatment with the DAG-mimetic PdBu increased the levels of HSP27 phosphorylation at S82 in wild-type DT40 B cells. BCR and phorbol ester signals were also able to increase HSP27 phosphorylation in PKD1 or PKD3 single knockout DT40 B cells (Fig. 1B). However, BCR- and phorbol ester-induced phosphorylation of HSP27 on S82 was abolished in B cells that lacked both PKD1 and PKD3 (Fig. 1C). Significantly, doxycycline-induced expression of the Flag-PKD3 transgene in the double knockout cells was sufficient to restore normal regulation of HSP27 phosphorylation (Fig. 1C). In contrast, expression of a kinase-deficient PKD3 mutant protein in the double knockout cells was not able to restore BCR- or phorbol ester-induced HSP27 phosphorylation (Fig. 1D). Hence, PKD3 as well as PKD1 can regulate HSP27 phosphorylation and in DT40 B cells they are functionally redundant as HSP27 kinases. 3.2 Cellular proliferation and survival in DT40 B cells lacking expression of PKD family kinases PKD enzymes have previously been linked to the regulation of cell proliferation and survival (reviewed in [20]). To investigate the effect that loss of PKD kinases had on B cell survival and/or proliferation we cultured wild-type and PKD-null cells in the presence (PKD1/3−/−: Flag-PKD3+ve) or absence (PKD1/3−/−) of doxycycline and monitored exponential growth. As shown in Fig. 2A, PKD1/3−/− cells proliferated exponentially and re-expression of Flag-PKD3 in these cells had no impact on the rate of proliferation. Furthermore, the viability of PKD1/3−/− B cells during routine culturing was not significantly different from that of wild-type B cells (data not shown). It was noted that the population doubling time of PKD1/3−/− cells was slightly slower than that of wild type DT40 cells (12.7 ± 2.8 h versus 10.2 ± 0.4 h) but the failure of PKD3 re-expression to modify the proliferation rate of PKD1/3−/− cells suggests that these small differences were most likely the result of clonal variation and were not caused specifically by loss of PKD enzymes. Thus, PKD family enzymes are not essential for regulating basal survival and proliferation of DT40 B cells. PKD enzymes, specifically PKD1 and PKD2, have previously been linked to a protective role against oxidative stress-induced injury in 3T3 fibroblast, HeLa and epithelial cell lines [17,30–32]. We therefore addressed the role of PKD family kinases in regulating B cell survival in response to oxidative stress and other stress stimuli. As shown in Fig. 2B, loss of PKD1/3 expression had no significant impact on the survival of DT40 B cells in response to mitochondrial stress stimuli (H2O2 or serum deprivation); DNA damaging agents (etoposide or doxorubicin); ER pathway stress due to calcium overload (thapsigargin) or following prolonged treatment with phorbol esters or Trichostatin A, an inhibitor of class I/II HDACs. Thus, PKD kinases do not play an essential role in regulating B cell survival in response to a range of different stress stimuli. 3.3 ",receptor
R4622 T5769 T5770 compound Antigen,receptor
R4623 T5770 T5773 amod receptor,pathways
R4624 T5771 T5773 amod regulated,pathways
R4625 T5772 T5773 amod signalling,pathways
R4626 T5773 T5781 nsubj pathways,explore
R4627 T5774 T5773 prep in,pathways
R4628 T5775 T5777 compound PKD-null,B
R4629 T5776 T5777 compound DT40,B
R4630 T5777 T5778 compound B,cells
R4631 T5778 T5774 pobj cells,in
R4632 T5779 T5781 aux To,explore
R4633 T5780 T5781 advmod further,explore
R4634 T5781 T5781 ROOT explore,explore
R4635 T5782 T5783 det the,contribution
R4636 T5783 T5781 dobj contribution,explore
R4637 T5784 T5783 prep of,contribution
R4638 T5785 T5786 compound PKD,kinases
R4639 T5786 T5784 pobj kinases,of
R4640 T5787 T5786 prep to,kinases
R4641 T5788 T5791 compound DT40,biology
R4642 T5789 T5791 compound B,biology
R4643 T5790 T5791 compound cell,biology
R4644 T5791 T5787 pobj biology,to
R4645 T5792 T5793 nsubj we,investigated
R4646 T5793 T5783 relcl investigated,contribution
R4647 T5794 T5799 mark whether,were
R4648 T5795 T5798 amod specific,events
R4649 T5796 T5798 amod BCR-regulated,events
R4650 T5797 T5798 amod signalling,events
R4651 T5798 T5799 nsubj events,were
R4652 T5799 T5793 ccomp were,investigated
R4653 T5800 T5799 acomp defective,were
R4654 T5801 T5800 prep in,defective
R4655 T5802 T5805 det the,cells
R4656 T5803 T5804 compound PKD-null,B
R4657 T5804 T5805 compound B,cells
R4658 T5805 T5801 pobj cells,in
R4659 T5806 T5781 punct .,explore
R4660 T5807 T5808 amod Initial,experiments
R4661 T5808 T5809 nsubj experiments,revealed
R4662 T5809 T5809 ROOT revealed,revealed
R4663 T5810 T5817 mark that,reduced
R4664 T5811 T5812 compound surface,expression
R4665 T5812 T5817 nsubjpass expression,reduced
R4666 T5813 T5812 prep of,expression
R4667 T5814 T5815 det the,BCR
R4668 T5815 T5813 pobj BCR,of
R4669 T5816 T5817 auxpass was,reduced
R4670 T5817 T5809 ccomp reduced,revealed
R4671 T5818 T5817 prep in,reduced
R4672 T5819 T5822 nummod PKD1/3,−
R4673 T5820 T5822 nummod −,−
R4674 T5821 T5822 compound /,−
R4675 T5822 T5818 pobj −,in
R4676 T5823 T5822 punct (,−
R4677 T5824 T5818 cc and,in
R4678 T5825 T5817 prep in,reduced
R4679 T5826 T5835 nummod PKD1/3,cells
R4680 T5827 T5829 nummod −,−
R4681 T5828 T5829 compound /,−
R4682 T5829 T5835 nummod −,cells
R4683 T5830 T5829 punct :,−
R4684 T5831 T5829 appos Flag-PKD3,−
R4685 T5832 T5833 advmod +,ve
R4686 T5833 T5829 appos ve,−
R4687 T5834 T5829 punct ),−
R4688 T5835 T5825 pobj cells,in
R4689 T5836 T5817 prep compared,reduced
R4690 T5837 T5836 prep to,compared
R4691 T5838 T5841 amod wild-type,cells
R4692 T5839 T5840 compound DT40,B
R4693 T5840 T5841 compound B,cells
R4694 T5841 T5837 pobj cells,to
R4695 T5842 T5841 punct (,cells
R4696 T5843 T5844 compound Fig.,3A
R4697 T5844 T5841 appos 3A,cells
R4698 T5845 T5844 cc and,3A
R4699 T5846 T5848 nsubj data,shown
R4700 T5847 T5848 neg not,shown
R4701 T5848 T5841 relcl shown,cells
R4702 T5849 T5817 punct ),reduced
R4703 T5850 T5809 punct .,revealed
R4704 T5851 T5860 advmod Nevertheless,was
R4705 T5852 T5860 punct ",",was
R4706 T5853 T5860 nsubj BCR-crosslinking,was
R4707 T5854 T5853 prep of,BCR-crosslinking
R4708 T5855 T5859 nummod PKD1/3,cells
R4709 T5856 T5859 nummod −,cells
R4710 T5857 T5859 nmod /,cells
R4711 T5858 T5859 amod −,cells
R4712 T5859 T5854 pobj cells,of
R4713 T5860 T5860 ROOT was,was
R4714 T5861 T5860 acomp sufficient,was
R4715 T5862 T5863 aux to,induce
R4716 T5863 T5861 xcomp induce,sufficient
R4717 T5864 T5865 det the,activation
R4718 T5865 T5863 dobj activation,induce
R4719 T5866 T5865 prep of,activation
R4720 T5867 T5868 det a,number
R4721 T5868 T5866 pobj number,of
R4722 T5869 T5868 prep of,number
R4723 T5870 T5869 pcomp signalling,of
R4724 T5871 T5870 dobj cascades,signalling
R4725 T5872 T5871 punct ",",cascades
R4726 T5873 T5871 amod similar,cascades
R4727 T5874 T5873 prep to,similar
R4728 T5875 T5876 nsubj that,observed
R4729 T5876 T5871 relcl observed,cascades
R4730 T5877 T5876 prep in,observed
R4731 T5878 T5879 amod wild-type,cells
R4732 T5879 T5877 pobj cells,in
R4733 T5880 T5871 punct (,cascades
R4734 T5881 T5882 compound Fig.,3B
R4735 T5882 T5871 appos 3B,cascades
R4736 T5883 T5871 punct ),cascades
R4737 T5884 T5860 punct .,was
R4738 T5885 T5888 advmod Hence,activation
R4739 T5886 T5888 punct ",",activation
R4740 T5887 T5888 amod BCR-induced,activation
R4741 T5888 T5909 nsubj activation,was
R4742 T5889 T5888 prep of,activation
R4743 T5890 T5891 det the,Akt
R4744 T5891 T5889 pobj Akt,of
R4745 T5892 T5891 punct ",",Akt
R4746 T5893 T5895 compound mTOR/p70,kinase
R4747 T5894 T5895 compound S6,kinase
R4748 T5895 T5891 appos kinase,Akt
R4749 T5896 T5898 punct (,shown
R4750 T5897 T5898 mark as,shown
R4751 T5898 T5888 advcl shown,activation
R4752 T5899 T5898 agent by,shown
R4753 T5900 T5908 nummod S6,pathways
R4754 T5901 T5902 amod ribosomal,protein
R4755 T5902 T5908 nmod protein,pathways
R4756 T5903 T5902 appos phosphorylation,protein
R4757 T5904 T5902 punct ),protein
R4758 T5905 T5902 cc and,protein
R4759 T5906 T5902 conj MAPK,protein
R4760 T5907 T5908 amod signalling,pathways
R4761 T5908 T5899 pobj pathways,by
R4762 T5909 T5909 ROOT was,was
R4763 T5910 T5909 advmod clearly,was
R4764 T5911 T5909 acomp detectable,was
R4765 T5912 T5911 prep in,detectable
R4766 T5913 T5914 compound PKD1/3-null,B
R4767 T5914 T5915 compound B,cells
R4768 T5915 T5912 pobj cells,in
R4769 T5916 T5918 punct (,3B
R4770 T5917 T5918 compound Fig.,3B
R4771 T5918 T5911 appos 3B,detectable
R4772 T5919 T5918 punct ),3B
R4773 T5920 T5909 punct .,was
R4774 T5921 T5941 advmod Furthermore,observed
R4775 T5922 T5941 punct ",",observed
R4776 T5923 T5925 amod enhanced,phosphorylation
R4777 T5924 T5925 compound tyrosine,phosphorylation
R4778 T5925 T5941 nsubjpass phosphorylation,observed
R4779 T5926 T5925 prep of,phosphorylation
R4780 T5927 T5929 amod multiple,proteins
R4781 T5928 T5929 amod cellular,proteins
R4782 T5929 T5926 pobj proteins,of
R4783 T5930 T5932 advmod as,as
R4784 T5931 T5932 advmod well,as
R4785 T5932 T5925 cc as,phosphorylation
R4786 T5933 T5934 det an,increase
R4787 T5934 T5925 conj increase,phosphorylation
R4788 T5935 T5934 prep in,increase
R4789 T5936 T5938 amod intracellular,levels
R4790 T5937 T5938 compound calcium,levels
R4791 T5938 T5935 pobj levels,in
R4792 T5939 T5941 auxpass was,observed
R4793 T5940 T5941 advmod also,observed
R4794 T5941 T5941 ROOT observed,observed
R4795 T5942 T5941 prep following,observed
R4796 T5943 T5944 compound BCR,stimulation
R4797 T5944 T5942 pobj stimulation,following
R4798 T5945 T5944 prep of,stimulation
R4799 T5946 T5948 nmod PKD1/3-null,cells
R4800 T5947 T5948 compound B,cells
R4801 T5948 T5945 pobj cells,of
R4802 T5949 T5950 punct (,data
R4803 T5950 T5948 appos data,cells
R4804 T5951 T5952 neg not,shown
R4805 T5952 T5950 acl shown,data
R4806 T5953 T5950 punct ),data
R4807 T5954 T5941 punct .,observed
R4808 T5955 T5957 nsubj We,observe
R4809 T5956 T5957 aux did,observe
R4810 T5957 T5957 ROOT observe,observe
R4811 T5958 T5970 mark that,induced
R4812 T5959 T5960 det the,strength
R4813 T5960 T5970 nsubj strength,induced
R4814 T5961 T5960 prep of,strength
R4815 T5962 T5961 pobj BCR,of
R4816 T5963 T5960 punct (,strength
R4817 T5964 T5960 cc but,strength
R4818 T5965 T5966 neg not,phorbol
R4819 T5966 T5967 advmod phorbol,ester
R4820 T5967 T5960 conj ester,strength
R4821 T5968 T5960 punct ),strength
R4822 T5969 T5970 punct -,induced
R4823 T5970 T5957 ccomp induced,observe
R4824 T5971 T5970 dobj regulation,induced
R4825 T5972 T5971 prep of,regulation
R4826 T5973 T5976 det the,pathway
R4827 T5974 T5976 amod Erk1-RSK1,pathway
R4828 T5975 T5976 compound signalling,pathway
R4829 T5976 T5972 pobj pathway,of
R4830 T5977 T5978 auxpass was,reduced
R4831 T5978 T5970 conj reduced,induced
R4832 T5979 T5978 prep in,reduced
R4833 T5980 T5985 nummod PKD1/3,cells
R4834 T5981 T5985 nummod −,cells
R4835 T5982 T5985 compound /,cells
R4836 T5983 T5985 compound −,cells
R4837 T5984 T5985 compound B,cells
R4838 T5985 T5979 pobj cells,in
R4839 T5986 T5978 prep compared,reduced
R4840 T5987 T5986 prep to,compared
R4841 T5988 T5990 amod wild-type,cells
R4842 T5989 T5990 compound B,cells
R4843 T5990 T5987 pobj cells,to
R4844 T5991 T5993 punct (,3B
R4845 T5992 T5993 compound Fig.,3B
R4846 T5993 T5990 appos 3B,cells
R4847 T5994 T5990 punct ),cells
R4848 T5995 T5957 punct .,observe
R4849 T5996 T5997 nummod One,interpretation
R4850 T5997 T6001 nsubj interpretation,is
R4851 T5998 T5997 prep of,interpretation
R4852 T5999 T6000 det this,data
R4853 T6000 T5998 pobj data,of
R4854 T6001 T6001 ROOT is,is
R4855 T6002 T6006 mark that,modulate
R4856 T6003 T6004 compound PKD,enzymes
R4857 T6004 T6006 nsubj enzymes,modulate
R4858 T6005 T6006 aux may,modulate
R4859 T6006 T6001 ccomp modulate,is
R4860 T6007 T6008 compound Erk,activation
R4861 T6008 T6006 dobj activation,modulate
R4862 T6009 T6001 punct .,is
R4863 T6010 T6017 advmod Indeed,linked
R4864 T6011 T6017 punct ",",linked
R4865 T6012 T6013 compound PKD,enzymes
R4866 T6013 T6017 nsubj enzymes,linked
R4867 T6014 T6017 aux have,linked
R4868 T6015 T6017 advmod previously,linked
R4869 T6016 T6017 auxpass been,linked
R4870 T6017 T6017 ROOT linked,linked
R4871 T6018 T6017 prep to,linked
R4872 T6019 T6020 det the,growth
R4873 T6020 T6018 pobj growth,to
R4874 T6021 T6023 amod factor-regulated,signalling
R4875 T6022 T6023 compound Erk,signalling
R4876 T6023 T6017 dobj signalling,linked
R4877 T6024 T6023 prep in,signalling
R4878 T6025 T6029 nmod fibroblast,lines
R4879 T6026 T6025 cc and,fibroblast
R4880 T6027 T6029 amod endothelial,lines
R4881 T6028 T6029 compound cell,lines
R4882 T6029 T6024 pobj lines,in
R4883 T6030 T6023 dobj [,signalling
R4884 T6031 T6030 nummod 33,[
R4885 T6032 T6033 nummod 35,]
R4886 T6033 T6030 appos ],[
R4887 T6034 T6017 punct .,linked
R4888 T6035 T6042 advmod However,reduced
R4889 T6036 T6042 punct ",",reduced
R4890 T6037 T6039 amod BCR-induced,phosphorylation
R4891 T6038 T6039 compound Erk,phosphorylation
R4892 T6039 T6042 nsubjpass phosphorylation,reduced
R4893 T6040 T6042 auxpass was,reduced
R4894 T6041 T6042 advmod also,reduced
R4895 T6042 T6042 ROOT reduced,reduced
R4896 T6043 T6042 prep in,reduced
R4897 T6044 T6052 nummod PKD1/3,cells
R4898 T6045 T6046 nummod −,/
R4899 T6046 T6052 compound /,cells
R4900 T6047 T6049 punct −,Flag-PKD3
R4901 T6048 T6049 punct -,Flag-PKD3
R4902 T6049 T6052 compound Flag-PKD3,cells
R4903 T6050 T6052 compound +,cells
R4904 T6051 T6052 compound B,cells
R4905 T6052 T6043 pobj cells,in
R4906 T6053 T6052 punct (,cells
R4907 T6054 T6054 ROOT data,data
R4908 T6055 T6056 neg not,shown
R4909 T6056 T6054 acl shown,data
R4910 T6057 T6054 punct ),data
R4911 T6058 T6042 advcl suggesting,reduced
R4912 T6059 T6074 mark that,−
R4913 T6060 T6062 amod reduced,levels
R4914 T6061 T6062 compound BCR,levels
R4915 T6062 T6074 nsubj levels,−
R4916 T6063 T6062 prep on,levels
R4917 T6064 T6065 det the,surface
R4918 T6065 T6063 pobj surface,on
R4919 T6066 T6065 prep of,surface
R4920 T6067 T6070 nummod PKD1/3,−
R4921 T6068 T6070 nummod −,−
R4922 T6069 T6070 compound /,−
R4923 T6070 T6066 pobj −,of
R4924 T6071 T6070 punct (,−
R4925 T6072 T6070 cc and,−
R4926 T6073 T6074 nsubj PKD1/3,−
R4927 T6074 T6058 ccomp −,suggesting
R4928 T6075 T6079 nummod /,+
R4929 T6076 T6078 punct −,Flag-PKD3
R4930 T6077 T6078 punct -,Flag-PKD3
R4931 T6078 T6079 compound Flag-PKD3,+
R4932 T6079 T6074 appos +,−
R4933 T6080 T6074 punct ),−
R4934 T6081 T6082 amod B,cells
R4935 T6082 T6085 nsubj cells,impact
R4936 T6083 T6085 aux may,impact
R4937 T6084 T6085 nsubj itself,impact
R4938 T6085 T6085 ROOT impact,impact
R4939 T6086 T6085 prep on,impact
R4940 T6087 T6088 det the,strength
R4941 T6088 T6086 pobj strength,on
R4942 T6089 T6088 prep of,strength
R4943 T6090 T6089 pobj activation,of
R4944 T6091 T6090 prep of,activation
R4945 T6092 T6096 det this,pathway
R4946 T6093 T6096 amod specific,pathway
R4947 T6094 T6096 amod intracellular,pathway
R4948 T6095 T6096 compound signalling,pathway
R4949 T6096 T6091 pobj pathway,of
R4950 T6097 T6085 punct .,impact
R4951 T6098 T6099 aux To,search
R4952 T6099 T6120 advcl search,used
R4953 T6100 T6099 prep for,search
R4954 T6101 T6104 amod other,targets
R4955 T6102 T6104 amod potential,targets
R4956 T6103 T6104 compound PKD,targets
R4957 T6104 T6100 pobj targets,for
R4958 T6105 T6107 nsubj that,show
R4959 T6106 T6107 aux may,show
R4960 T6107 T6104 relcl show,targets
R4961 T6108 T6109 amod defective,regulation
R4962 T6109 T6107 dobj regulation,show
R4963 T6110 T6109 prep in,regulation
R4964 T6111 T6116 compound PKD1/3,B
R4965 T6112 T6116 compound −,B
R4966 T6113 T6116 compound /,B
R4967 T6114 T6116 compound −,B
R4968 T6115 T6116 compound DT40,B
R4969 T6116 T6117 compound B,cells
R4970 T6117 T6110 pobj cells,in
R4971 T6118 T6120 punct ",",used
R4972 T6119 T6120 nsubj we,used
R4973 T6120 T6120 ROOT used,used
R4974 T6121 T6123 det a,substrate
R4975 T6122 T6123 compound PKD,substrate
R4976 T6123 T6120 dobj substrate,used
R4977 T6124 T6123 amod phospho-antibody,substrate
R4978 T6125 T6126 nsubj that,recognises
R4979 T6126 T6124 relcl recognises,phospho-antibody
R4980 T6127 T6129 compound consensus,sequences
R4981 T6128 T6129 compound phosphorylation,sequences
R4982 T6129 T6126 dobj sequences,recognises
R4983 T6130 T6129 acl targeted,sequences
R4984 T6131 T6130 agent by,targeted
R4985 T6132 T6133 compound PKD,enzymes
R4986 T6133 T6131 pobj enzymes,by
R4987 T6134 T6137 punct (,[
R4988 T6135 T6137 nmod LxRxxpS/T,[
R4989 T6136 T6137 punct ),[
R4990 T6137 T6133 appos [,enzymes
R4991 T6138 T6139 nummod 36,]
R4992 T6139 T6137 appos ],[
R4993 T6140 T6120 punct .,used
R4994 T6141 T6142 mark As,shown
R4995 T6142 T6160 advcl shown,was
R4996 T6143 T6142 prep in,shown
R4997 T6144 T6145 compound Fig.,3C
R4998 T6145 T6143 pobj 3C,in
R4999 T6146 T6145 punct ",",3C
R5000 T6147 T6160 nsubj phorbol,was
R5001 T6148 T6160 nsubj ester,was
R5002 T6149 T6148 punct -,ester
R5003 T6150 T6148 cc and,ester
R5004 T6151 T6152 amod BCR-induced,phosphorylation
R5005 T6152 T6148 conj phosphorylation,ester
R5006 T6153 T6152 prep of,phosphorylation
R5007 T6154 T6155 amod cellular,substrates
R5008 T6155 T6153 pobj substrates,of
R5009 T6156 T6155 acl detected,substrates
R5010 T6157 T6156 agent by,detected
R5011 T6158 T6159 det this,phospho-antibody
R5012 T6159 T6157 pobj phospho-antibody,by
R5013 T6160 T6160 ROOT was,was
R5014 T6161 T6160 acomp similar,was
R5015 T6162 T6161 prep in,similar
R5016 T6163 T6169 amod wild-type,cells
R5017 T6164 T6163 cc and,wild-type
R5018 T6165 T6163 conj PKD1/3,wild-type
R5019 T6166 T6169 compound −,cells
R5020 T6167 T6169 compound /,cells
R5021 T6168 T6169 compound −,cells
R5022 T6169 T6162 pobj cells,in
R5023 T6170 T6160 cc and,was
R5024 T6171 T6160 conj is,was
R5025 T6172 T6173 advmod therefore,independent
R5026 T6173 T6171 acomp independent,is
R5027 T6174 T6173 prep of,independent
R5028 T6175 T6176 compound PKD,enzymes
R5029 T6176 T6174 pobj enzymes,of
R5030 T6177 T6171 punct .,is
R5031 T6178 T6201 advmod However,prevented
R5032 T6179 T6201 punct ",",prevented
R5033 T6180 T6201 nsubj pretreatment,prevented
R5034 T6181 T6180 prep of,pretreatment
R5035 T6182 T6183 preconj both,wild-type
R5036 T6183 T6181 pobj wild-type,of
R5037 T6184 T6183 cc and,wild-type
R5038 T6185 T6183 conj PKD1/3,wild-type
R5039 T6186 T6188 compound −,−
R5040 T6187 T6188 compound /,−
R5041 T6188 T6191 compound −,cells
R5042 T6189 T6190 compound DT40,B
R5043 T6190 T6191 compound B,cells
R5044 T6191 T6183 appos cells,wild-type
R5045 T6192 T6180 prep with,pretreatment
R5046 T6193 T6192 pobj GF109203X,with
R5047 T6194 T6193 punct ",",GF109203X
R5048 T6195 T6197 det a,derivative
R5049 T6196 T6197 compound bisindoylmaleimide,derivative
R5050 T6197 T6193 appos derivative,GF109203X
R5051 T6198 T6199 nsubj that,inhibits
R5052 T6199 T6197 relcl inhibits,derivative
R5053 T6200 T6199 dobj PKCs,inhibits
R5054 T6201 T6201 ROOT prevented,prevented
R5055 T6202 T6203 det the,induction
R5056 T6203 T6201 dobj induction,prevented
R5057 T6204 T6203 prep of,induction
R5058 T6205 T6204 pobj proteins,of
R5059 T6206 T6207 nsubj that,contain
R5060 T6207 T6205 relcl contain,proteins
R5061 T6208 T6209 compound phosphorylated,LxRxxS/T
R5062 T6209 T6210 compound LxRxxS/T,motifs
R5063 T6210 T6207 dobj motifs,contain
R5064 T6211 T6201 punct .,prevented
R5065 T6212 T6216 advmod Thus,enzymes
R5066 T6213 T6216 nsubj loss,enzymes
R5067 T6214 T6213 prep of,loss
R5068 T6215 T6214 pobj PKD1/3,of
R5069 T6216 T6220 nsubj enzymes,disrupt
R5070 T6217 T6220 aux does,disrupt
R5071 T6218 T6220 neg not,disrupt
R5072 T6219 T6220 advmod globally,disrupt
R5073 T6220 T6220 ROOT disrupt,disrupt
R5074 T6221 T6222 det the,phosphorylation
R5075 T6222 T6220 dobj phosphorylation,disrupt
R5076 T6223 T6222 prep of,phosphorylation
R5077 T6224 T6225 amod cellular,proteins
R5078 T6225 T6223 pobj proteins,of
R5079 T6226 T6227 nsubj that,contain
R5080 T6227 T6225 relcl contain,proteins
R5081 T6228 T6229 compound LxRxxpS/T,motifs
R5082 T6229 T6227 dobj motifs,contain
R5083 T6230 T6220 punct .,disrupt
R5084 T6231 T6232 det This,result
R5085 T6232 T6233 nsubj result,is
R5086 T6233 T6233 ROOT is,is
R5087 T6234 T6236 advmod perhaps,surprising
R5088 T6235 T6236 neg not,surprising
R5089 T6236 T6233 acomp surprising,is
R5090 T6237 T6241 mark as,act
R5091 T6238 T6239 compound LxRxxS/T,motifs
R5092 T6239 T6241 nsubj motifs,act
R5093 T6240 T6241 advmod also,act
R5094 T6241 T6236 advcl act,surprising
R5095 T6242 T6241 prep as,act
R5096 T6243 T6244 amod good,substrates
R5097 T6244 T6242 pobj substrates,as
R5098 T6245 T6244 prep for,substrates
R5099 T6246 T6248 amod other,kinases
R5100 T6247 T6248 amod serine/threonine,kinases
R5101 T6248 T6245 pobj kinases,for
R5102 T6249 T6250 amod such,as
R5103 T6250 T6248 prep as,kinases
R5104 T6251 T6250 pobj MAPKAPK2,as
R5105 T6252 T6233 punct .,is
R5106 T6253 T6257 advmod However,provide
R5107 T6254 T6255 det these,experiments
R5108 T6255 T6257 nsubj experiments,provide
R5109 T6256 T6257 aux do,provide
R5110 T6257 T6257 ROOT provide,provide
R5111 T6258 T6259 amod further,evidence
R5112 T6259 T6257 dobj evidence,provide
R5113 T6260 T6263 mark that,are
R5114 T6261 T6262 amod phosphospecific,antisera
R5115 T6262 T6263 nsubj antisera,are
R5116 T6263 T6259 acl are,evidence
R5117 T6264 T6263 neg not,are
R5118 T6265 T6266 advmod sufficiently,selective
R5119 T6266 T6263 acomp selective,are
R5120 T6267 T6269 aux to,designated
R5121 T6268 T6269 auxpass be,designated
R5122 T6269 T6266 xcomp designated,selective
R5123 T6270 T6269 oprd kinase,designated
R5124 T6271 T6273 amod specific,antisera
R5125 T6272 T6273 compound substrate,antisera
R5126 T6273 T6270 appos antisera,kinase
R5127 T6274 T6257 punct .,provide
R5128 T6275 T6277 amod BCR-induced,pathways
R5129 T6276 T6277 amod signalling,pathways
R5130 T6277 T6278 nsubj pathways,culminate
R5131 T6278 T6278 ROOT culminate,culminate
R5132 T6279 T6278 prep in,culminate
R5133 T6280 T6281 det the,activation
R5134 T6281 T6279 pobj activation,in
R5135 T6282 T6281 prep of,activation
R5136 T6283 T6284 compound gene,transcription
R5137 T6284 T6285 compound transcription,events
R5138 T6285 T6282 pobj events,of
R5139 T6286 T6287 nsubj that,control
R5140 T6287 T6285 relcl control,events
R5141 T6288 T6290 compound B,survival
R5142 T6289 T6290 compound cell,survival
R5143 T6290 T6287 dobj survival,control
R5144 T6291 T6290 punct ",",survival
R5145 T6292 T6290 conj proliferation,survival
R5146 T6293 T6292 cc and,proliferation
R5147 T6294 T6292 conj function,proliferation
R5148 T6295 T6278 punct .,culminate
R5149 T6296 T6303 prep In,proposed
R5150 T6297 T6298 det this,context
R5151 T6298 T6296 pobj context,In
R5152 T6299 T6303 punct ",",proposed
R5153 T6300 T6303 nsubjpass it,proposed
R5154 T6301 T6303 aux has,proposed
R5155 T6302 T6303 auxpass been,proposed
R5156 T6303 T6303 ROOT proposed,proposed
R5157 T6304 T6303 dobj that,proposed
R5158 T6305 T6307 compound PKD,members
R5159 T6306 T6307 compound family,members
R5160 T6307 T6304 nsubj members,that
R5161 T6308 T6307 dobj control,members
R5162 T6309 T6308 prep of,control
R5163 T6310 T6311 compound gene,transcription
R5164 T6311 T6309 pobj transcription,of
R5165 T6312 T6307 prep through,members
R5166 T6313 T6312 pobj activation,through
R5167 T6314 T6313 prep of,activation
R5168 T6315 T6318 det the,factor
R5169 T6316 T6318 compound NFκB,factor
R5170 T6317 T6318 compound transcription,factor
R5171 T6318 T6314 pobj factor,of
R5172 T6319 T6303 punct .,proposed
R5173 T6320 T6326 advmod Thus,occurs
R5174 T6321 T6326 punct ",",occurs
R5175 T6322 T6323 amod PKD-mediated,activation
R5176 T6323 T6326 nsubj activation,occurs
R5177 T6324 T6323 prep of,activation
R5178 T6325 T6324 pobj NFκB,of
R5179 T6326 T6326 ROOT occurs,occurs
R5180 T6327 T6326 advmod downstream,occurs
R5181 T6328 T6327 prep of,downstream
R5182 T6329 T6330 det a,variety
R5183 T6330 T6328 pobj variety,of
R5184 T6331 T6330 prep of,variety
R5185 T6332 T6333 amod different,signals
R5186 T6333 T6331 pobj signals,of
R5187 T6334 T6333 punct ",",signals
R5188 T6335 T6333 prep including,signals
R5189 T6336 T6337 amod mROS/oxidative,stress
R5190 T6337 T6335 pobj stress,including
R5191 T6338 T6337 punct ",",stress
R5192 T6339 T6340 amod lysophosphatidic,acid
R5193 T6340 T6337 conj acid,stress
R5194 T6341 T6340 cc and,acid
R5195 T6342 T6344 det the,oncogene
R5196 T6343 T6344 compound Bcr-Abl,oncogene
R5197 T6344 T6340 conj oncogene,acid
R5198 T6345 T6347 compound [,]
R5199 T6346 T6347 compound "17,21,23,30,37",]
R5200 T6347 T6344 appos ],oncogene
R5201 T6348 T6326 punct .,occurs
R5202 T6349 T6357 advmod Furthermore,enhances
R5203 T6350 T6351 punct ",",expression
R5204 T6351 T6357 nsubj expression,enhances
R5205 T6352 T6351 prep of,expression
R5206 T6353 T6356 det an,mutant
R5207 T6354 T6356 amod activated,mutant
R5208 T6355 T6356 compound PKD1,mutant
R5209 T6356 T6352 pobj mutant,of
R5210 T6357 T6357 ROOT enhances,enhances
R5211 T6358 T6360 amod HPK1-mediated,activation
R5212 T6359 T6360 compound NFκB,activation
R5213 T6360 T6357 dobj activation,enhances
R5214 T6361 T6363 nmod [,]
R5215 T6362 T6363 nummod 38,]
R5216 T6363 T6357 npadvmod ],enhances
R5217 T6364 T6357 punct .,enhances
R5218 T6365 T6371 prep In,known
R5219 T6366 T6367 compound B,cells
R5220 T6367 T6365 pobj cells,In
R5221 T6368 T6371 punct ",",known
R5222 T6369 T6371 nsubjpass NFκB,known
R5223 T6370 T6371 auxpass is,known
R5224 T6371 T6371 ROOT known,known
R5225 T6372 T6374 aux to,regulated
R5226 T6373 T6374 auxpass be,regulated
R5227 T6374 T6371 xcomp regulated,known
R5228 T6375 T6374 prep via,regulated
R5229 T6376 T6375 pobj DAG,via
R5230 T6377 T6376 cc and,DAG
R5231 T6378 T6379 compound PKCβ,[
R5232 T6379 T6376 conj [,DAG
R5233 T6380 T6381 compound "39,40",]
R5234 T6381 T6376 conj ],DAG
R5235 T6382 T6371 cc but,known
R5236 T6383 T6385 mark whether,are
R5237 T6384 T6385 nsubj PKDs,are
R5238 T6385 T6371 conj are,known
R5239 T6386 T6387 amod key,intermediaries
R5240 T6387 T6385 attr intermediaries,are
R5241 T6388 T6385 prep for,are
R5242 T6389 T6390 compound NFκB,regulation
R5243 T6406 T6409 nsubjpass activity,induced
R5244 T6390 T6388 pobj regulation,for
R5245 T6407 T6409 auxpass was,induced
R5246 T6408 T6409 advmod strongly,induced
R5247 T6391 T6394 aux has,explored
R5248 T6409 T6402 ccomp induced,show
R5249 T6410 T6409 prep in,induced
R5250 T6392 T6394 neg not,explored
R5251 T6411 T6412 preconj both,wild-type
R5252 T6393 T6394 auxpass been,explored
R5253 T6412 T6417 nmod wild-type,−
R5254 T6394 T6385 conj explored,are
R5255 T6413 T6412 cc and,wild-type
R5256 T6414 T6412 conj PKD1/3,wild-type
R5257 T6415 T6417 compound −,−
R5258 T6395 T6371 punct .,known
R5259 T6416 T6417 compound /,−
R5260 T6417 T6420 compound −,cells
R5261 T6418 T6419 compound DT40,B
R5262 T6396 T6397 det The,data
R5263 T6419 T6420 compound B,cells
R5264 T6420 T6410 pobj cells,in
R5265 T6421 T6409 prep in,induced
R5266 T6397 T6402 nsubj data,show
R5267 T6422 T6421 pobj response,in
R5268 T6423 T6422 prep to,response
R5269 T6398 T6397 punct (,data
R5270 T6424 T6426 preconj either,ester
R5271 T6425 T6426 compound phorbol,ester
R5272 T6399 T6400 compound Fig.,4A
R5273 T6426 T6423 pobj ester,to
R5274 T6427 T6426 cc or,ester
R5275 T6428 T6429 compound BCR,stimulation
R5276 T6429 T6426 conj stimulation,ester
R5277 T6430 T6402 punct .,show
R5278 T6431 T6442 prep In,abolished
R5279 T6432 T6431 pobj contrast,In
R5280 T6400 T6397 appos 4A,data
R5281 T6433 T6442 punct ",",abolished
R5282 T6434 T6440 nmod BCR,activity
R5283 T6401 T6397 punct ),data
R5284 T6435 T6434 cc and,BCR
R5285 T6436 T6440 amod phorbol,activity
R5286 T6437 T6440 amod ester-induced,activity
R5287 T6438 T6440 nmod NFκB,activity
R5288 T6439 T6440 amod transcriptional,activity
R5289 T6402 T6402 ROOT show,show
R5290 T6440 T6442 nsubjpass activity,abolished
R5291 T6441 T6442 auxpass was,abolished
R5292 T6403 T6409 mark that,induced
R5293 T6442 T6442 ROOT abolished,abolished
R5294 T6443 T6442 prep in,abolished
R5295 T6444 T6449 compound PKCβ,B
R5296 T6404 T6406 nmod NFκB,activity
R5297 T6445 T6449 compound −,B
R5298 T6446 T6449 compound /,B
R5299 T6447 T6449 compound −,B
R5300 T6405 T6406 amod transcriptional,activity
R5301 T6448 T6449 compound DT40,B
R5302 T6449 T6450 compound B,cells
R5303 T6503 T6500 pobj cells,in
R5304 T6450 T6443 pobj cells,in
R5305 T6451 T6442 punct (,abolished
R5306 T6504 T6496 cc and,mediate
R5307 T6505 T6508 advmod hence,participate
R5308 T6452 T6453 compound Fig.,4A
R5309 T6506 T6508 aux do,participate
R5310 T6453 T6442 npadvmod 4A,abolished
R5311 T6454 T6442 punct ),abolished
R5312 T6455 T6442 punct ",",abolished
R5313 T6456 T6473 mark although,observed
R5314 T6507 T6508 neg not,participate
R5315 T6457 T6458 amod strong,activation
R5316 T6458 T6473 nsubjpass activation,observed
R5317 T6508 T6496 conj participate,mediate
R5318 T6459 T6458 prep of,activation
R5319 T6460 T6461 compound PKD,kinases
R5320 T6461 T6459 pobj kinases,of
R5321 T6509 T6508 prep in,participate
R5322 T6462 T6464 punct (,assessed
R5323 T6463 T6464 mark as,assessed
R5324 T6510 T6509 pobj DAG/PKC,in
R5325 T6464 T6473 advcl assessed,observed
R5326 T6465 T6464 agent by,assessed
R5327 T6466 T6465 pobj autophosphorylation,by
R5328 T6467 T6466 prep of,autophosphorylation
R5329 T6468 T6467 pobj PKD1,of
R5330 T6469 T6466 prep at,autophosphorylation
R5331 T6470 T6469 pobj S916,at
R5332 T6471 T6464 punct ),assessed
R5333 T6472 T6473 auxpass was,observed
R5334 T6511 T6490 conj mediated,are
R5335 T6473 T6442 advcl observed,abolished
R5336 T6474 T6473 prep in,observed
R5337 T6512 T6511 dobj control,mediated
R5338 T6475 T6477 det the,−
R5339 T6476 T6477 compound PKCβ,−
R5340 T6477 T6474 pobj −,in
R5341 T6478 T6442 conj /,abolished
R5342 T6513 T6512 prep of,control
R5343 T6479 T6480 nummod −,cells
R5344 T6480 T6478 dobj cells,/
R5345 T6481 T6483 punct (,4B
R5346 T6514 T6513 pobj NFκB,of
R5347 T6482 T6483 compound Fig.,4B
R5348 T6483 T6478 parataxis 4B,/
R5349 T6484 T6483 punct ),4B
R5350 T6515 T6490 punct .,are
R5351 T6485 T6442 punct .,abolished
R5353 T6486 T6490 advmod Thus,are
R5354 T6487 T6490 punct ",",are
R5355 T6488 T6489 compound PKD,kinases
R5356 T6489 T6490 nsubj kinases,are
R5357 T6490 T6490 ROOT are,are
R5358 T6491 T6492 advmod neither,essential
R5359 T6492 T6490 acomp essential,are
R5360 T6493 T6492 cc nor,essential
R5361 T6494 T6492 conj sufficient,essential
R5362 T6495 T6496 aux to,mediate
R5363 T6496 T6494 xcomp mediate,sufficient
R5364 T6497 T6499 amod BCR-induced,activation
R5365 T6498 T6499 compound NFκB,activation
R5366 T6499 T6496 dobj activation,mediate
R5367 T6500 T6499 prep in,activation
R5368 T6501 T6502 compound DT40,B
R5369 T6502 T6503 compound B,cells
R5864 T7377 T7381 amod "40 B-lymphocyte cell line. Previously we have shown that PKDs have an essential role in regulating class II histone deacetylases in DT40 B-cells [Matthews, S.A., Liu, P., Spitaler, M., Olson, E.N., McKinsey, T.A., Cantrell, D.A. and Scharenberg, A.M. (2006) Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes. Mol. Cell Biol. 26, 1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. Most cell types express at least two PKD isoforms but PKD enzymes are especially highly expressed in haematopoietic cells, where they are activated in response to antigen receptors stimulation [2,3]. A conserved signalling pathway linking antigen receptors to PKDs involves the activation of PLCγ and the subsequent production of diacylglycerol (DAG) which stimulates classical and/or novel protein kinase Cs (PKC) that phosphorylate two key regulatory serine residues in the activation loop of PKD kinases [3–6]. The N-terminal regulatory region of PKD enzymes contains a DAG binding domain and direct binding of DAG also contributes to PKD1 activation [7] as well as regulating the spatial location of PKD enzymes within cells [8–12]. PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). In particular, PKDs have been widely linked to the activation of the NFκB transcription factor and in regulating cell survival during oxidative stress [17,21–23]. Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. An essential role for PKD enzymes in regulating class II histone deacetylases (HDACs), enzymes that repress MEF2-dependent gene transcription, has also been demonstrated [1,26–28]. To investigate the biological role of PKDs we have generated DT40 B cell lines that lack expression of one or more members of the PKD family [1], allowing us to investigate the function(s) of PKD isoforms following B cell antigen receptor (BCR) stimulation, as well addressing the issue of functional redundancy between the different PKD family members. Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. However, PKD-null DT40 B cells are viable and proliferate normally. Moreover, loss of the entire cellular pool of PKD does not critically affect oxidative stress responses in B cells nor do PKD kinases play an essential role in regulating NFκB transcriptional activity. Together, these findings reveal that in B lymphocytes, PKD kinases are not critical regulators of many of the cellular processes previously ascribed to them in other cellular systems. 2 Materials and methods 2.1 Cell culture, transient transfections and cell stimulation The generation, culture and activation of PKD1−/−, PKD3−/− and PKD1/3−/− knockout DT40 B cell lines have been described previously [1]. Cells were lysed and protein extracts were analysed in Western blotting experiments as previously described [1]. Chloramphenicol acetyl transferase assays have been described previously [29]. 2.2 sIgM staining DT40 B cells (2 × 106 cells per point) were resuspended in 200 μl buffer (RPMI 1640 media, 1% foetal calf serum) containing anti-chicken M1 monoclonal antibody conjugated to FITC for 20 min on ice. The cells were washed twice and fluorescent intensity was analysed by flow cytometry. All results shown are representative of at two to four independent experiments unless otherwise indicated. 3 Results 3.1 Loss of HSP27 phosphorylation in DT40 B cells lacking expression of PKD family kinases DT40 B cells express two PKD isoforms, PKD1 and PKD3, and as previously described we have recently generated DT40 B cell lines that lack expression of either PKD1 or PKD3 or both enzymes [1]. In generating the double knockout cell lines we targeted the PKD1 loci in a PKD3−/− cell line that expressed a Flag-PKD3 transgene under the control of a doxycycline-inducible promoter. Hence, in the presence of doxycycline, Flag-PKD3 expression in PKD1/3 double knockout cells is comparable to endogenous PKD3 present in wild-type DT40 cells and removal of doxycycline from the culture media for 5 days results in a completely null PKD phenotype (Fig. 1A). Previously, we have demonstrated that phosphorylation and nuclear exclusion of class II histone deacetylases (HDACs) during BCR engagement is defective in PKD1/3−/− B cells and can restored upon re-expression of a single PKD isoform [1]. The small heat shock protein HSP27 has recently been proposed as a PKD1 substrate [24] and we accordingly assessed whether PKD-null DT40 cells have defective phosphorylation of HSP27 on serine 82, the proposed PKD1 substrate sequence. We initially investigated the regulation of HSP27 phosphorylation in single knockout DT40 B cells lacking either PKD1 or PKD3. As shown in Fig. 1B, activation of the BCR or treatment with the DAG-mimetic PdBu increased the levels of HSP27 phosphorylation at S82 in wild-type DT40 B cells. BCR and phorbol ester signals were also able to increase HSP27 phosphorylation in PKD1 or PKD3 single knockout DT40 B cells (Fig. 1B). However, BCR- and phorbol ester-induced phosphorylation of HSP27 on S82 was abolished in B cells that lacked both PKD1 and PKD3 (Fig. 1C). Significantly, doxycycline-induced expression of the Flag-PKD3 transgene in the double knockout cells was sufficient to restore normal regulation of HSP27 phosphorylation (Fig. 1C). In contrast, expression of a kinase-deficient PKD3 mutant protein in the double knockout cells was not able to restore BCR- or phorbol ester-induced HSP27 phosphorylation (Fig. 1D). Hence, PKD3 as well as PKD1 can regulate HSP27 phosphorylation and in DT40 B cells they are functionally redundant as HSP27 kinases. 3.2 Cellular proliferation and survival in DT40 B cells lacking expression of PKD family kinases PKD enzymes have previously been linked to the regulation of cell proliferation and survival (reviewed in [20]). To investigate the effect that loss of PKD kinases had on B cell survival and/or proliferation we cultured wild-type and PKD-null cells in the presence (PKD1/3−/−: Flag-PKD3+ve) or absence (PKD1/3−/−) of doxycycline and monitored exponential growth. As shown in Fig. 2A, PKD1/3−/− cells proliferated exponentially and re-expression of Flag-PKD3 in these cells had no impact on the rate of proliferation. Furthermore, the viability of PKD1/3−/− B cells during routine culturing was not significantly different from that of wild-type B cells (data not shown). It was noted that the population doubling time of PKD1/3−/− cells was slightly slower than that of wild type DT40 cells (12.7 ± 2.8 h versus 10.2 ± 0.4 h) but the failure of PKD3 re-expression to modify the proliferation rate of PKD1/3−/− cells suggests that these small differences were most likely the result of clonal variation and were not caused specifically by loss of PKD enzymes. Thus, PKD family enzymes are not essential for regulating basal survival and proliferation of DT40 B cells. PKD enzymes, specifically PKD1 and PKD2, have previously been linked to a protective role against oxidative stress-induced injury in 3T3 fibroblast, HeLa and epithelial cell lines [17,30–32]. We therefore addressed the role of PKD family kinases in regulating B cell survival in response to oxidative stress and other stress stimuli. As shown in Fig. 2B, loss of PKD1/3 expression had no significant impact on the survival of DT40 B cells in response to mitochondrial stress stimuli (H2O2 or serum deprivation); DNA damaging agents (etoposide or doxorubicin); ER pathway stress due to calcium overload (thapsigargin) or following prolonged treatment with phorbol esters or Trichostatin A, an inhibitor of class I/II HDACs. Thus, PKD kinases do not play an essential role in regulating B cell survival in response to a range of different stress stimuli. 3.3 Antigen receptor regulated signalling pathways in PKD-null DT40 B cells To further explore the contribution of PKD kinases to DT40 B cell biology we investigated whether specific BCR-regulated signalling events were defective in the PKD-null B cells. Initial experiments revealed that surface expression of the BCR was reduced in PKD1/3−/− (and in PKD1/3−/−:Flag-PKD3+ve) cells compared to wild-type DT40 B cells (Fig. 3A and data not shown). Nevertheless, BCR-crosslinking of PKD1/3−/− cells was sufficient to induce the activation of a number of signalling cascades, similar to that observed in wild-type cells (Fig. 3B). Hence, BCR-induced activation of the Akt, mTOR/p70 S6 kinase (as shown by S6 ribosomal protein phosphorylation) and MAPK signalling pathways was clearly detectable in PKD1/3-null B cells (Fig. 3B). Furthermore, enhanced tyrosine phosphorylation of multiple cellular proteins as well as an increase in intracellular calcium levels was also observed following BCR stimulation of PKD1/3-null B cells (data not shown). We did observe that the strength of BCR (but not phorbol ester)-induced regulation of the Erk1-RSK1 signalling pathway was reduced in PKD1/3−/− B cells compared to wild-type B cells (Fig. 3B). One interpretation of this data is that PKD enzymes may modulate Erk activation. Indeed, PKD enzymes have previously been linked to the growth factor-regulated Erk signalling in fibroblast and endothelial cell lines [33–35]. However, BCR-induced Erk phosphorylation was also reduced in PKD1/3−/−-Flag-PKD3+ B cells (data not shown) suggesting that reduced BCR levels on the surface of PKD1/3−/− (and PKD1/3−/−-Flag-PKD3+) B cells may itself impact on the strength of activation of this specific intracellular signalling pathway. To search for other potential PKD targets that may show defective regulation in PKD1/3−/− DT40 B cells, we used a PKD substrate phospho-antibody that recognises consensus phosphorylation sequences targeted by PKD enzymes (LxRxxpS/T) [36]. As shown in Fig. 3C, phorbol ester- and BCR-induced phosphorylation of cellular substrates detected by this phospho-antibody was similar in wild-type and PKD1/3−/− cells and is therefore independent of PKD enzymes. However, pretreatment of both wild-type and PKD1/3−/− DT40 B cells with GF109203X, a bisindoylmaleimide derivative that inhibits PKCs prevented the induction of proteins that contain phosphorylated LxRxxS/T motifs. Thus loss of PKD1/3 enzymes does not globally disrupt the phosphorylation of cellular proteins that contain LxRxxpS/T motifs. This result is perhaps not surprising as LxRxxS/T motifs also act as good substrates for other serine/threonine kinases such as MAPKAPK2. However these experiments do provide further evidence that phosphospecific antisera are not sufficiently selective to be designated kinase specific substrate antisera. BCR-induced signalling pathways culminate in the activation of gene transcription events that control B cell survival, proliferation and function. In this context, it has been proposed that PKD family members control of gene transcription through activation of the NFκB transcription factor. Thus, PKD-mediated activation of NFκB occurs downstream of a variety of different signals, including mROS/oxidative stress, lysophosphatidic acid and the Bcr-Abl oncogene [17,21,23,30,37]. Furthermore, expression of an activated PKD1 mutant enhances HPK1-mediated NFκB activation [38]. In B cells, NFκB is known to be regulated via DAG and PKCβ [39,40] but whether PKDs are key intermediaries for NFκB regulation has not been explored. The data (Fig. 4A) show that NFκB transcriptional activity was strongly induced in both wild-type and PKD1/3−/− DT40 B cells in response to either phorbol ester or BCR stimulation. In contrast, BCR and phorbol ester-induced NFκB transcriptional activity was abolished in PKCβ−/− DT40 B cells (Fig. 4A), although strong activation of PKD kinases (as assessed by autophosphorylation of PKD1 at S916) was observed in the PKCβ−/− cells (Fig. 4B). Thus, PKD kinases are neither essential nor sufficient to mediate BCR-induced NFκB activation in DT40 B cells and hence do not participate in DAG/PKC mediated control of NFκB. 4 Discussion Protein",kinases
R5865 T7378 T7381 compound kinase,kinases
R5866 T7379 T7381 compound D,kinases
R5867 T7380 T7381 compound serine,kinases
R5868 T7381 T7384 nsubjpass kinases,proposed
R5869 T7382 T7384 aux have,proposed
R5870 T7383 T7384 auxpass been,proposed
R5871 T7384 T7384 ROOT proposed,proposed
R5872 T7385 T7386 aux to,regulate
R5873 T7386 T7384 xcomp regulate,proposed
R5874 T7387 T7389 amod diverse,functions
R5875 T7388 T7389 amod cellular,functions
R5876 T7389 T7386 dobj functions,regulate
R5877 T7390 T7389 prep including,functions
R5878 T7391 T7392 det the,phosphorylation
R5879 T7392 T7390 pobj phosphorylation,including
R5880 T7393 T7392 cc and,phosphorylation
R5881 T7394 T7395 amod nuclear,localisation
R5882 T7395 T7392 conj localisation,phosphorylation
R5883 T7396 T7395 prep of,localisation
R5884 T7397 T7399 compound class,HDACs
R5885 T7398 T7399 compound II,HDACs
R5886 T7399 T7396 pobj HDACs,of
R5887 T7400 T7399 cc and,HDACs
R5888 T7401 T7402 det the,phosphorylation
R5889 T7402 T7399 conj phosphorylation,HDACs
R5890 T7403 T7402 prep of,phosphorylation
R5891 T7404 T7403 pobj HSP27,of
R5892 T7405 T7384 punct .,proposed
R5893 T7406 T7410 nsubj It,suggested
R5894 T7407 T7410 aux has,suggested
R5895 T7408 T7410 advmod also,suggested
R5896 T7409 T7410 auxpass been,suggested
R5897 T7410 T7410 ROOT suggested,suggested
R5898 T7411 T7413 mark that,act
R5899 T7412 T7413 nsubj PKDs,act
R5900 T7413 T7410 ccomp act,suggested
R5901 T7414 T7413 prep as,act
R5902 T7415 T7416 amod mitochondrial,sensors
R5903 T7416 T7414 pobj sensors,as
R5904 T7417 T7416 prep for,sensors
R5905 T7418 T7419 amod oxidative,stress
R5906 T7419 T7417 pobj stress,for
R5907 T7420 T7413 cc and,act
R5908 T7421 T7413 conj play,act
R5909 T7422 T7423 det a,role
R5910 T7423 T7421 dobj role,play
R5911 T7424 T7423 prep in,role
R5912 T7425 T7424 pcomp regulating,in
R5913 T7426 T7427 compound NFκB,transcription
R5914 T7427 T7428 compound transcription,factors
R5915 T7428 T7425 dobj factors,regulating
R5916 T7429 T7431 nmod [,]
R5917 T7430 T7431 nummod 41,]
R5918 T7431 T7428 appos ],factors
R5919 T7432 T7410 punct .,suggested
R5920 T7433 T7443 nsubj Most,come
R5921 T7434 T7433 prep of,Most
R5922 T7435 T7436 det the,data
R5923 T7436 T7434 pobj data,of
R5924 T7437 T7436 prep about,data
R5925 T7438 T7439 det the,function
R5926 T7439 T7437 pobj function,about
R5927 T7440 T7439 prep of,function
R5928 T7441 T7440 pobj PKDs,of
R5929 T7442 T7443 aux has,come
R5930 T7443 T7443 ROOT come,come
R5931 T7444 T7443 prep from,come
R5932 T7445 T7444 pobj experiments,from
R5933 T7446 T7448 nsubj that,express
R5934 T7447 T7448 advmod ectopically,express
R5935 T7448 T7445 relcl express,experiments
R5936 T7449 T7453 amod active,mutants
R5937 T7450 T7449 cc or,active
R5938 T7451 T7449 conj inhibitory,active
R5939 T7452 T7453 compound PKD,mutants
R5940 T7453 T7448 dobj mutants,express
R5941 T7454 T7453 cc or,mutants
R5942 T7455 T7456 det that,use
R5943 T7456 T7453 conj use,mutants
R5944 T7457 T7456 dobj RNAi,use
R5945 T7458 T7459 aux to,reduce
R5946 T7459 T7456 xcomp reduce,use
R5947 T7460 T7461 compound PKD,expression
R5948 T7461 T7459 dobj expression,reduce
R5949 T7462 T7443 punct .,come
R5950 T7463 T7465 nsubj We,used
R5951 T7464 T7465 aux have,used
R5952 T7465 T7465 ROOT used,used
R5953 T7466 T7465 dobj gene,used
R5954 T7467 T7466 acl targeting,gene
R5955 T7468 T7470 aux to,delete
R5956 T7469 T7470 advmod specifically,delete
R5957 T7470 T7467 xcomp delete,targeting
R5958 T7471 T7472 compound PKD,alleles
R5959 T7472 T7470 dobj alleles,delete
R5960 T7473 T7470 prep in,delete
R5961 T7474 T7477 compound DT40,cells
R5962 T7475 T7476 compound chicken,B
R5963 T7476 T7477 compound B,cells
R5964 T7477 T7473 pobj cells,in
R5965 T7478 T7470 cc and,delete
R5966 T7479 T7481 aux can,use
R5967 T7480 T7481 advmod thus,use
R5968 T7481 T7470 conj use,delete
R5969 T7482 T7483 compound PKD-null,DT40
R5970 T7483 T7484 compound DT40,cells
R5971 T7484 T7481 dobj cells,use
R5972 T7485 T7486 aux to,assess
R5973 T7486 T7481 xcomp assess,use
R5974 T7487 T7489 det the,contribution
R5975 T7488 T7489 amod relative,contribution
R5976 T7489 T7486 dobj contribution,assess
R5977 T7490 T7489 prep of,contribution
R5978 T7491 T7493 amod individual,isoforms
R5979 T7492 T7493 compound PKD,isoforms
R5980 T7493 T7490 pobj isoforms,of
R5981 T7494 T7493 prep in,isoforms
R5982 T7495 T7494 pobj class,in
R5983 T7496 T7497 compound II,HDAC
R5984 T7497 T7498 compound HDAC,control
R5985 T7498 T7489 conj control,contribution
R5986 T7499 T7498 prep versus,control
R5987 T7500 T7502 amod oxidative,responses
R5988 T7501 T7502 compound stress,responses
R5989 T7502 T7499 pobj responses,versus
R5990 T7503 T7502 cc and,responses
R5991 T7504 T7505 compound NFκB,regulation
R5992 T7505 T7502 conj regulation,responses
R5993 T7506 T7505 prep in,regulation
R5994 T7507 T7506 pobj lymphocytes,in
R5995 T7508 T7465 punct .,used
R5996 T7509 T7512 nsubj We,used
R5997 T7510 T7512 aux have,used
R5998 T7511 T7512 advmod previously,used
R5999 T7512 T7512 ROOT used,used
R6000 T7513 T7516 det these,cells
R6001 T7514 T7515 compound PKD-null,DT40
R6002 T7515 T7516 compound DT40,cells
R6003 T7516 T7512 dobj cells,used
R6004 T7517 T7518 aux to,define
R6005 T7518 T7512 xcomp define,used
R6006 T7519 T7521 det an,role
R6007 T7520 T7521 amod essential,role
R6008 T7521 T7518 dobj role,define
R6009 T7522 T7521 prep for,role
R6010 T7523 T7522 pobj PKDs,for
R6011 T7524 T7523 prep in,PKDs
R6012 T7525 T7524 pobj regulation,in
R6013 T7526 T7525 prep of,regulation
R6014 T7527 T7529 compound class,HDACs
R6015 T7528 T7529 compound II,HDACs
R6016 T7529 T7526 pobj HDACs,of
R6017 T7530 T7535 punct ",",describes
R6018 T7531 T7533 det the,report
R6019 T7532 T7533 amod present,report
R6020 T7533 T7535 nsubj report,describes
R6021 T7534 T7535 advmod now,describes
R6022 T7535 T7512 conj describes,used
R6023 T7536 T7538 det an,role
R6024 T7537 T7538 amod indispensable,role
R6025 T7538 T7535 dobj role,describes
R6026 T7539 T7538 prep for,role
R6027 T7540 T7539 pobj PKDs,for
R6028 T7541 T7540 prep in,PKDs
R6029 T7542 T7541 pcomp regulating,in
R6030 T7543 T7544 det the,phosphorylation
R6031 T7544 T7542 dobj phosphorylation,regulating
R6032 T7545 T7544 prep of,phosphorylation
R6033 T7546 T7545 pobj HSP27,of
R6034 T7547 T7544 prep on,phosphorylation
R6035 T7548 T7547 pobj serine,on
R6036 T7549 T7548 nummod 82,serine
R6037 T7550 T7548 punct ",",serine
R6038 T7551 T7552 det a,site
R6039 T7552 T7542 dobj site,regulating
R6040 T7553 T7554 advmod previously,identified
R6041 T7554 T7552 acl identified,site
R6042 T7555 T7554 prep as,identified
R6043 T7556 T7557 det a,target
R6044 T7557 T7555 pobj target,as
R6045 T7558 T7557 prep for,target
R6046 T7559 T7562 det the,cascade
R6047 T7560 T7561 advmod p38-MAPKAPK2,signalling
R6048 T7561 T7562 amod signalling,cascade
R6049 T7562 T7558 pobj cascade,for
R6050 T7563 T7565 nmod [,]
R6051 T7564 T7565 nummod 42,]
R6052 T7565 T7562 appos ],cascade
R6053 T7566 T7535 punct .,describes
R6054 T7567 T7574 advmod However,reveal
R6055 T7568 T7574 punct ",",reveal
R6056 T7569 T7574 nsubj studies,reveal
R6057 T7570 T7569 prep of,studies
R6058 T7571 T7572 compound PKD-null,DT40
R6059 T7572 T7573 compound DT40,cells
R6060 T7573 T7570 pobj cells,of
R6061 T7574 T7574 ROOT reveal,reveal
R6062 T7575 T7579 mark that,are
R6063 T7576 T7578 compound PKD,kinases
R6064 T7577 T7578 compound family,kinases
R6065 T7578 T7579 nsubj kinases,are
R6066 T7579 T7574 ccomp are,reveal
R6067 T7580 T7579 neg not,are
R6068 T7581 T7579 acomp essential,are
R6069 T7582 T7581 prep for,essential
R6070 T7583 T7586 amod oxidative,responses
R6071 T7584 T7585 compound stress,survival
R6072 T7585 T7586 compound survival,responses
R6073 T7586 T7582 pobj responses,for
R6074 T7587 T7579 cc nor,are
R6075 T7588 T7590 auxpass are,required
R6076 T7589 T7590 nsubjpass they,required
R6077 T7590 T7579 conj required,are
R6078 T7591 T7590 prep for,required
R6079 T7592 T7591 pobj activation,for
R6080 T7593 T7592 prep of,activation
R6081 T7594 T7596 compound NFκB,factors
R6082 T7595 T7596 compound transcription,factors
R6083 T7596 T7593 pobj factors,of
R6084 T7597 T7574 punct .,reveal
R6085 T7598 T7600 det These,findings
R6086 T7599 T7600 amod latter,findings
R6087 T7600 T7601 nsubj findings,are
R6088 T7601 T7601 ROOT are,are
R6089 T7602 T7601 prep in,are
R6090 T7603 T7604 amod striking,contrast
R6091 T7604 T7602 pobj contrast,in
R6092 T7605 T7604 prep to,contrast
R6093 T7606 T7607 amod previous,observations
R6094 T7607 T7605 pobj observations,to
R6095 T7608 T7607 prep in,observations
R6096 T7609 T7613 nmod HeLa,lines
R6097 T7610 T7609 cc and,HeLa
R6098 T7611 T7613 amod epithelial,lines
R6099 T7612 T7613 compound cell,lines
R6100 T7613 T7608 pobj lines,in
R6101 T7614 T7618 advmod where,implicated
R6102 T7615 T7616 compound overexpression/RNAi,approaches
R6103 T7616 T7618 nsubj approaches,implicated
R6104 T7617 T7618 aux have,implicated
R6105 T7618 T7613 relcl implicated,lines
R6106 T7619 T7618 dobj PKD1/2,implicated
R6107 T7620 T7618 prep in,implicated
R6108 T7621 T7622 det the,control
R6109 T7622 T7620 pobj control,in
R6110 T7623 T7622 prep of,control
R6111 T7624 T7623 pobj proliferation,of
R6112 T7625 T7624 punct ",",proliferation
R6113 T7626 T7624 conj survival,proliferation
R6114 T7627 T7626 cc and,survival
R6115 T7628 T7629 compound NFκB,activation
R6116 T7629 T7626 conj activation,survival
R6117 T7630 T7632 compound [,]
R6118 T7631 T7632 compound "20,23",]
R6119 T7632 T7622 appos ],control
R6120 T7633 T7601 punct .,are
R6121 T7634 T7639 advmod Hence,shows
R6122 T7635 T7639 punct ",",shows
R6123 T7636 T7638 det the,report
R6124 T7637 T7638 amod present,report
R6125 T7638 T7639 nsubj report,shows
R6126 T7639 T7639 ROOT shows,shows
R6127 T7640 T7664 mark that,are
R6128 T7641 T7643 det the,roles
R6129 T7642 T7643 amod proposed,roles
R6130 T7643 T7664 nsubj roles,are
R6131 T7644 T7643 prep for,roles
R6132 T7645 T7644 pobj PKDs,for
R6133 T7646 T7664 mark as,are
R6134 T7647 T7648 amod key,sensors
R6135 T7648 T7646 pobj sensors,as
R6136 T7649 T7650 nsubj that,modulate
R6137 T7650 T7648 relcl modulate,sensors
R6138 T7651 T7652 compound survival,pathways
R6139 T7652 T7650 dobj pathways,modulate
R6140 T7653 T7650 prep in,modulate
R6141 T7654 T7653 pobj response,in
R6142 T7655 T7654 prep to,response
R6143 T7656 T7657 amod oxidative,stress
R6144 T7657 T7655 pobj stress,to
R6145 T7658 T7650 cc and,modulate
R6146 T7659 T7650 conj regulate,modulate
R6147 T7660 T7661 compound cell,survival
R6148 T7661 T7659 dobj survival,regulate
R6149 T7662 T7661 cc and,survival
R6150 T7663 T7661 conj proliferation,survival
R6151 T7664 T7639 ccomp are,shows
R6152 T7665 T7664 neg not,are
R6153 T7666 T7664 acomp ubiquitous,are
R6154 T7667 T7664 cc and,are
R6155 T7668 T7670 aux may,restricted
R6156 T7669 T7670 auxpass be,restricted
R6157 T7670 T7664 conj restricted,are
R6158 T7671 T7670 prep to,restricted
R6159 T7672 T7674 amod certain,lineages
R6160 T7673 T7674 compound cell,lineages
R6161 T7674 T7671 pobj lineages,to
R6162 T7675 T7639 punct .,shows
R6163 T7676 T7681 advcl Taken,indicate
R6164 T7677 T7676 advmod together,Taken
R6165 T7678 T7681 punct ",",indicate
R6166 T7679 T7680 det these,data
R6167 T7680 T7681 nsubj data,indicate
R6168 T7681 T7681 ROOT indicate,indicate
R6169 T7682 T7693 mark that,impact
R6170 T7683 T7693 nsubj loss,impact
R6171 T7684 T7683 prep of,loss
R6172 T7685 T7684 pobj expression,of
R6173 T7686 T7685 prep of,expression
R6174 T7687 T7689 compound PKD,members
R6175 T7688 T7689 compound family,members
R6176 T7689 T7686 pobj members,of
R6177 T7690 T7693 aux does,impact
R6178 T7691 T7693 neg not,impact
R6179 T7692 T7693 advmod globally,impact
R6180 T7693 T7681 ccomp impact,indicate
R6181 T7694 T7693 prep on,impact
R6182 T7695 T7698 amod early,pathways
R6183 T7696 T7698 amod BCR-regulated,pathways
R6184 T7697 T7698 compound signalling,pathways
R6185 T7698 T7694 pobj pathways,on
R6186 T7699 T7681 punct .,indicate
R894 T1008 T1011 amod "1569–1577]. We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. However, in contrast to previous observations in other cell types, PKD enzymes do not regulate basic cellular processes such as proliferation or survival responses, nor NFκB transcriptional activity downstream of the B cell antigen receptor. Thus, PKDs have a selective role in DT40 B-cell biology. 1 Introduction The",D
R895 T1009 T1011 nmod protein,D
R896 T1010 T1011 compound kinase,D
R897 T1011 T1011 ROOT D,D
R898 T1012 T1011 punct (,D
R899 T1013 T1011 appos PKD,D
R900 T1014 T1011 punct ),D
R901 T1015 T1017 amod serine/threonine,family
R902 T1016 T1017 compound kinase,family
R903 T1017 T1018 nsubj family,has
R904 T1018 T1018 ROOT has,has
R905 T1019 T1020 nummod three,members
R906 T1020 T1018 dobj members,has
R907 T1021 T1018 punct :,has
R908 T1022 T1022 ROOT PKD1,PKD1
R909 T1023 T1022 punct ",",PKD1
R910 T1024 T1022 conj PKD2,PKD1
R911 T1025 T1024 cc and,PKD2
R912 T1026 T1024 conj PKD3,PKD2
R913 T1027 T1018 punct .,has
R914 T1028 T1030 amod Most,types
R915 T1029 T1030 compound cell,types
R916 T1030 T1031 nsubj types,express
R917 T1031 T1031 ROOT express,express
R918 T1032 T1033 advmod at,least
R919 T1033 T1034 advmod least,two
R920 T1034 T1036 nummod two,isoforms
R921 T1035 T1036 compound PKD,isoforms
R922 T1036 T1031 dobj isoforms,express
R923 T1037 T1031 cc but,express
R924 T1038 T1039 compound PKD,enzymes
R925 T1039 T1040 nsubj enzymes,are
R926 T1040 T1043 auxpass are,expressed
R927 T1041 T1042 advmod especially,highly
R928 T1042 T1043 advmod highly,expressed
R929 T1043 T1031 conj expressed,express
R930 T1044 T1043 prep in,expressed
R931 T1045 T1046 amod haematopoietic,cells
R932 T1046 T1044 pobj cells,in
R933 T1047 T1043 punct ",",expressed
R934 T1048 T1051 advmod where,activated
R935 T1049 T1051 nsubjpass they,activated
R936 T1050 T1051 auxpass are,activated
R937 T1051 T1043 advcl activated,expressed
R938 T1052 T1051 prep in,activated
R939 T1053 T1052 pobj response,in
R940 T1054 T1053 prep to,response
R941 T1055 T1056 compound antigen,receptors
R942 T1056 T1057 compound receptors,stimulation
R943 T1057 T1054 pobj stimulation,to
R944 T1058 T1060 compound [,]
R945 T1059 T1060 compound "2,3",]
R946 T1060 T1057 appos ],stimulation
R947 T1061 T1043 punct .,expressed
R948 T1062 T1065 det A,pathway
R949 T1063 T1065 amod conserved,pathway
R950 T1064 T1065 amod signalling,pathway
R951 T1065 T1071 nsubj pathway,involves
R952 T1066 T1065 acl linking,pathway
R953 T1067 T1068 compound antigen,receptors
R954 T1068 T1066 dobj receptors,linking
R955 T1069 T1066 prep to,linking
R956 T1070 T1069 pobj PKDs,to
R957 T1071 T1071 ROOT involves,involves
R958 T1072 T1073 det the,activation
R959 T1073 T1071 dobj activation,involves
R960 T1074 T1073 prep of,activation
R961 T1075 T1074 pobj PLCγ,of
R962 T1076 T1073 cc and,activation
R963 T1077 T1079 det the,production
R964 T1078 T1079 amod subsequent,production
R965 T1079 T1073 conj production,activation
R966 T1080 T1079 prep of,production
R967 T1081 T1080 pobj diacylglycerol,of
R968 T1082 T1083 punct (,DAG
R969 T1083 T1081 appos DAG,diacylglycerol
R970 T1084 T1081 punct ),diacylglycerol
R971 T1085 T1086 nsubj which,stimulates
R972 T1086 T1079 relcl stimulates,production
R973 T1087 T1090 amod classical,protein
R974 T1088 T1087 cc and/or,classical
R975 T1089 T1087 conj novel,classical
R976 T1090 T1092 compound protein,Cs
R977 T1091 T1092 compound kinase,Cs
R978 T1092 T1086 dobj Cs,stimulates
R979 T1093 T1092 punct (,Cs
R980 T1094 T1092 appos PKC,Cs
R981 T1095 T1092 punct ),Cs
R982 T1096 T1109 nsubj that,kinases
R983 T1097 T1096 aux phosphorylate,that
R984 T1098 T1102 nummod two,residues
R985 T1099 T1102 amod key,residues
R986 T1100 T1102 amod regulatory,residues
R987 T1101 T1102 compound serine,residues
R988 T1102 T1097 dobj residues,phosphorylate
R989 T1103 T1102 prep in,residues
R990 T1104 T1106 det the,loop
R991 T1105 T1106 compound activation,loop
R992 T1106 T1103 pobj loop,in
R993 T1107 T1106 prep of,loop
R994 T1108 T1107 pobj PKD,of
R995 T1109 T1079 relcl kinases,production
R996 T1110 T1109 dobj [,kinases
R997 T1111 T1110 nummod 3,[
R998 T1112 T1113 nummod 6,]
R999 T1113 T1079 appos ],production