Id |
Subject |
Object |
Predicate |
Lexical cue |
T14 |
0-135 |
Sentence |
denotes |
Protein kinase D enzymes are dispensable for proliferation, survival and antigen receptor-regulated NFκB activity in vertebrate B-cells |
T1 |
0-135 |
Sentence |
denotes |
Protein kinase D enzymes are dispensable for proliferation, survival and antigen receptor-regulated NFκB activity in vertebrate B-cells |
T2 |
138-146 |
Sentence |
denotes |
Abstract |
T15 |
147-263 |
Sentence |
denotes |
To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. |
T3 |
147-263 |
Sentence |
denotes |
To investigate the importance of protein kinase D (PKD) enzymes we generated a PKD-null DT40 B-lymphocyte cell line. |
T16 |
264-614 |
Sentence |
denotes |
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. |
T4 |
264-614 |
Sentence |
denotes |
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. |
T5 |
615-619 |
Sentence |
denotes |
Mol. |
T17 |
615-646 |
Sentence |
denotes |
Mol. Cell Biol. 26, 1569–1577]. |
T6 |
620-630 |
Sentence |
denotes |
Cell Biol. |
T7 |
631-646 |
Sentence |
denotes |
26, 1569–1577]. |
T489 |
635-1151 |
Sentence |
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 protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. |
T18 |
647-737 |
Sentence |
denotes |
We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. |
T8 |
647-737 |
Sentence |
denotes |
We now show that PKDs are also required to regulate HSP27 phosphorylation in DT40 B-cells. |
T19 |
738-979 |
Sentence |
denotes |
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. |
T9 |
738-979 |
Sentence |
denotes |
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. |
T20 |
980-1036 |
Sentence |
denotes |
Thus, PKDs have a selective role in DT40 B-cell biology. |
T10 |
980-1036 |
Sentence |
denotes |
Thus, PKDs have a selective role in DT40 B-cell biology. |
T11 |
1038-1053 |
Sentence |
denotes |
1 Introduction |
T12 |
1054-1151 |
Sentence |
denotes |
The protein kinase D (PKD) serine/threonine kinase family has three members: PKD1, PKD2 and PKD3. |
T490 |
1152-1351 |
Sentence |
denotes |
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]. |
T13 |
1152-1351 |
Sentence |
denotes |
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]. |
T491 |
1352-1665 |
Sentence |
denotes |
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]. |
T14 |
1352-1665 |
Sentence |
denotes |
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]. |
T492 |
1666-1888 |
Sentence |
denotes |
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]. |
T15 |
1666-1888 |
Sentence |
denotes |
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]. |
T493 |
1889-2061 |
Sentence |
denotes |
PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. |
T16 |
1889-2061 |
Sentence |
denotes |
PKD enzymes have been proposed to regulate numerous cellular functions, including cell proliferation [13–16], anti-apoptotic signals [17,18] and thymocyte development [19]. |
T494 |
2062-2223 |
Sentence |
denotes |
Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). |
T17 |
2062-2223 |
Sentence |
denotes |
Expression of mutant catalytically inactive and constitutively activated PKDs can also modify Golgi function, cell adhesion and cell motility (reviewed in [20]). |
T495 |
2224-2386 |
Sentence |
denotes |
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]. |
T18 |
2224-2386 |
Sentence |
denotes |
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]. |
T496 |
2387-2531 |
Sentence |
denotes |
Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. |
T19 |
2387-2531 |
Sentence |
denotes |
Another recently proposed PKD1 substrate is HSP27 [24], a small heat shock protein involved in regulating cell migration and cell survival [25]. |
T497 |
2532-2712 |
Sentence |
denotes |
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]. |
T20 |
2532-2712 |
Sentence |
denotes |
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]. |
T498 |
2713-3066 |
Sentence |
denotes |
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. |
T21 |
2713-3066 |
Sentence |
denotes |
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. |
T499 |
3067-3158 |
Sentence |
denotes |
Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. |
T22 |
3067-3158 |
Sentence |
denotes |
Previous studies have shown that PKDs are indispensable for HDAC regulation in B cells [1]. |
T500 |
3159-3244 |
Sentence |
denotes |
Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. |
T23 |
3159-3244 |
Sentence |
denotes |
Herein we show that PKDs are also indispensable for HSP27 phosphorylation in B cells. |
T501 |
3245-3312 |
Sentence |
denotes |
However, PKD-null DT40 B cells are viable and proliferate normally. |
T24 |
3245-3312 |
Sentence |
denotes |
However, PKD-null DT40 B cells are viable and proliferate normally. |
T502 |
3313-3514 |
Sentence |
denotes |
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. |
T25 |
3313-3514 |
Sentence |
denotes |
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. |
T503 |
3515-3698 |
Sentence |
denotes |
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. |
T26 |
3515-3698 |
Sentence |
denotes |
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. |
T27 |
3700-3724 |
Sentence |
denotes |
2 Materials and methods |