PubMed:7520914
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-126 | Sentence | denotes | CD14-mediated translocation of nuclear factor-kappa B induced by lipopolysaccharide does not require tyrosine kinase activity. |
| T2 | 127-374 | Sentence | denotes | During the course of serious bacterial infections, lipopolysaccharide (LPS) is believed to interact with macrophage receptors, resulting in the generation of inflammatory mediators and systemic symptoms including hemodynamic instability and shock. |
| T3 | 375-467 | Sentence | denotes | CD14, a glycosylphosphatidylinositol-linked antigen, functions as an LPS signaling receptor. |
| T4 | 468-602 | Sentence | denotes | A critical issue concerns the mechanism by which CD14, which has no transmembrane domain, transduces its signal following LPS binding. |
| T5 | 603-798 | Sentence | denotes | Recently, investigators have hypothesized that CD14-mediated signaling is effected through a receptor-associated tyrosine kinase (TK), suggesting a multicomponent receptor model of LPS signaling. |
| T6 | 799-950 | Sentence | denotes | Wild-type Chinese hamster ovary (CHO)-K1 cells can be activated by endotoxin to release arachidonate following transfection with human CD14 (CHO/CD14). |
| T7 | 951-1052 | Sentence | denotes | Nuclear translocation of cytosolic NF-kappa B is correlated with a number of LPS-inducible responses. |
| T8 | 1053-1210 | Sentence | denotes | We sought to determine if this pathway were present in CHO/CD14 cells and to elucidate the relationship of NF-kappa B activation to the CD14 receptor system. |
| T9 | 1211-1350 | Sentence | denotes | LPS-stimulated translocation of NF-kappa B in CHO/CD14 cells resembled the same response in the murine macrophage-like cell line RAW 264.7. |
| T10 | 1351-1624 | Sentence | denotes | Protein synthesis inhibitors and corticosteroids, which suppress arachidonate release and the synthesis of proinflammatory cytokines, had no effect on translocation of NF-kappa B in CHO/CD14 or RAW 264.7 cells, demonstrating that NF-kappa B translocation is an early event. |
| T11 | 1625-1824 | Sentence | denotes | Although TK activity was consistently observed by immunoblotting extracts from activated RAW 264.7 cells, LPS-induced phosphotyrosine residues were not observed from similarly treated CHO/CD14 cells. |
| T12 | 1825-2044 | Sentence | denotes | Furthermore, the TK inhibitors herbimycin A and genistein failed to inhibit translocation of NF-kappa B in CHO/CD14 or RAW 264.7 cells, although both of these agents inhibited LPS-induced TK activity in RAW 264.7 cells. |
| T13 | 2045-2166 | Sentence | denotes | These results imply that TK activity is not obligatory for CD14-mediated signal transduction to occur in response to LPS. |
| T1 | 0-126 | Sentence | denotes | CD14-mediated translocation of nuclear factor-kappa B induced by lipopolysaccharide does not require tyrosine kinase activity. |
| T2 | 127-374 | Sentence | denotes | During the course of serious bacterial infections, lipopolysaccharide (LPS) is believed to interact with macrophage receptors, resulting in the generation of inflammatory mediators and systemic symptoms including hemodynamic instability and shock. |
| T3 | 375-467 | Sentence | denotes | CD14, a glycosylphosphatidylinositol-linked antigen, functions as an LPS signaling receptor. |
| T4 | 468-602 | Sentence | denotes | A critical issue concerns the mechanism by which CD14, which has no transmembrane domain, transduces its signal following LPS binding. |
| T5 | 603-798 | Sentence | denotes | Recently, investigators have hypothesized that CD14-mediated signaling is effected through a receptor-associated tyrosine kinase (TK), suggesting a multicomponent receptor model of LPS signaling. |
| T6 | 799-950 | Sentence | denotes | Wild-type Chinese hamster ovary (CHO)-K1 cells can be activated by endotoxin to release arachidonate following transfection with human CD14 (CHO/CD14). |
| T7 | 951-1052 | Sentence | denotes | Nuclear translocation of cytosolic NF-kappa B is correlated with a number of LPS-inducible responses. |
| T8 | 1053-1210 | Sentence | denotes | We sought to determine if this pathway were present in CHO/CD14 cells and to elucidate the relationship of NF-kappa B activation to the CD14 receptor system. |
| T9 | 1211-1350 | Sentence | denotes | LPS-stimulated translocation of NF-kappa B in CHO/CD14 cells resembled the same response in the murine macrophage-like cell line RAW 264.7. |
| T10 | 1351-1624 | Sentence | denotes | Protein synthesis inhibitors and corticosteroids, which suppress arachidonate release and the synthesis of proinflammatory cytokines, had no effect on translocation of NF-kappa B in CHO/CD14 or RAW 264.7 cells, demonstrating that NF-kappa B translocation is an early event. |
| T11 | 1625-1824 | Sentence | denotes | Although TK activity was consistently observed by immunoblotting extracts from activated RAW 264.7 cells, LPS-induced phosphotyrosine residues were not observed from similarly treated CHO/CD14 cells. |
| T12 | 1825-2044 | Sentence | denotes | Furthermore, the TK inhibitors herbimycin A and genistein failed to inhibit translocation of NF-kappa B in CHO/CD14 or RAW 264.7 cells, although both of these agents inhibited LPS-induced TK activity in RAW 264.7 cells. |
| T13 | 2045-2166 | Sentence | denotes | These results imply that TK activity is not obligatory for CD14-mediated signal transduction to occur in response to LPS. |
jnlpba-st-training
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-4 | protein | denotes | CD14 |
| T2 | 31-53 | protein | denotes | nuclear factor-kappa B |
| T3 | 101-116 | protein | denotes | tyrosine kinase |
| T4 | 232-252 | protein | denotes | macrophage receptors |
| T5 | 375-379 | protein | denotes | CD14 |
| T6 | 383-426 | protein | denotes | glycosylphosphatidylinositol-linked antigen |
| T7 | 444-466 | protein | denotes | LPS signaling receptor |
| T8 | 517-521 | protein | denotes | CD14 |
| T9 | 536-556 | protein | denotes | transmembrane domain |
| T10 | 650-654 | protein | denotes | CD14 |
| T11 | 716-731 | protein | denotes | tyrosine kinase |
| T12 | 809-845 | cell_line | denotes | Chinese hamster ovary (CHO)-K1 cells |
| T13 | 934-938 | protein | denotes | CD14 |
| T14 | 940-948 | protein | denotes | CHO/CD14 |
| T15 | 1108-1122 | cell_line | denotes | CHO/CD14 cells |
| T16 | 1160-1170 | protein | denotes | NF-kappa B |
| T17 | 1189-1193 | protein | denotes | CD14 |
| T18 | 1243-1253 | protein | denotes | NF-kappa B |
| T19 | 1257-1271 | cell_line | denotes | CHO/CD14 cells |
| T20 | 1307-1339 | cell_line | denotes | murine macrophage-like cell line |
| T21 | 1340-1349 | cell_line | denotes | RAW 264.7 |
| T22 | 1458-1483 | protein | denotes | proinflammatory cytokines |
| T23 | 1519-1529 | protein | denotes | NF-kappa B |
| T24 | 1537-1541 | protein | denotes | CD14 |
| T25 | 1545-1560 | cell_line | denotes | RAW 264.7 cells |
| T26 | 1581-1591 | protein | denotes | NF-kappa B |
| T27 | 1714-1729 | cell_line | denotes | RAW 264.7 cells |
| T28 | 1809-1823 | cell_line | denotes | CHO/CD14 cells |
| T29 | 1918-1928 | protein | denotes | NF-kappa B |
| T30 | 1932-1940 | cell_line | denotes | CHO/CD14 |
| T31 | 1944-1959 | cell_line | denotes | RAW 264.7 cells |
| T32 | 2028-2043 | cell_line | denotes | RAW 264.7 cells |
| T33 | 2104-2108 | protein | denotes | CD14 |
genia-medco-coref
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| C1 | 65-83 | NP | denotes | lipopolysaccharide |
| C2 | 101-125 | NP | denotes | tyrosine kinase activity |
| C3 | 178-202 | NP | denotes | lipopolysaccharide (LPS) |
| C4 | 375-379 | NP | denotes | CD14 |
| C5 | 381-426 | NP | denotes | a glycosylphosphatidylinositol-linked antigen |
| C6 | 494-507 | NP | denotes | the mechanism |
| C7 | 511-516 | NP | denotes | which |
| C8 | 517-521 | NP | denotes | CD14 |
| C9 | 523-528 | NP | denotes | which |
| C10 | 569-572 | NP | denotes | its |
| C11 | 928-949 | NP | denotes | human CD14 (CHO/CD14) |
| C12 | 1108-1122 | NP | denotes | CHO/CD14 cells |
| C13 | 1257-1271 | NP | denotes | CHO/CD14 cells |
| C14 | 1303-1349 | NP | denotes | the murine macrophage-like cell line RAW 264.7 |
| C15 | 1351-1399 | NP | denotes | Protein synthesis inhibitors and corticosteroids |
| C16 | 1401-1406 | NP | denotes | which |
| C18 | 1533-1541 | NP | denotes | CHO/CD14 |
| C19 | 1545-1560 | NP | denotes | RAW 264.7 cells |
| C17 | 1502-1560 | NP | denotes | translocation of NF-kappa B in CHO/CD14 or RAW 264.7 cells |
| C20 | 1634-1645 | NP | denotes | TK activity |
| C22 | 1932-1940 | NP | denotes | CHO/CD14 |
| C23 | 1944-1959 | NP | denotes | RAW 264.7 cells |
| C21 | 1901-1959 | NP | denotes | translocation of NF-kappa B in CHO/CD14 or RAW 264.7 cells |
| C24 | 1970-1990 | NP | denotes | both of these agents |
| C25 | 2028-2043 | NP | denotes | RAW 264.7 cells |
| C26 | 2070-2081 | NP | denotes | TK activity |
| C27 | 2162-2165 | NP | denotes | LPS |
| R1 | C3 | C1 | coref-ident | lipopolysaccharide (LPS),lipopolysaccharide |
| R2 | C5 | C4 | coref-appos | a glycosylphosphatidylinositol-linked antigen,CD14 |
| R3 | C7 | C6 | coref-relat | which,the mechanism |
| R4 | C9 | C8 | coref-relat | which,CD14 |
| R5 | C10 | C8 | coref-pron | its,CD14 |
| R6 | C12 | C11 | coref-ident | CHO/CD14 cells,human CD14 (CHO/CD14) |
| R7 | C13 | C12 | coref-ident | CHO/CD14 cells,CHO/CD14 cells |
| R8 | C16 | C15 | coref-relat | which,Protein synthesis inhibitors and corticosteroids |
| R9 | C18 | C13 | coref-ident | CHO/CD14,CHO/CD14 cells |
| R10 | C19 | C14 | coref-ident | RAW 264.7 cells,the murine macrophage-like cell line RAW 264.7 |
| R11 | C20 | C2 | coref-ident | TK activity,tyrosine kinase activity |
| R12 | C22 | C18 | coref-ident | CHO/CD14,CHO/CD14 |
| R13 | C23 | C19 | coref-ident | RAW 264.7 cells,RAW 264.7 cells |
| R14 | C21 | C17 | coref-ident | translocation of NF-kappa B in CHO/CD14 or RAW 264.7 cells,translocation of NF-kappa B in CHO/CD14 or RAW 264.7 cells |
| R15 | C24 | C22 | coref-ident | both of these agents,CHO/CD14 |
| R16 | C24 | C23 | coref-ident | both of these agents,RAW 264.7 cells |
| R17 | C25 | C23 | coref-ident | RAW 264.7 cells,RAW 264.7 cells |
| R18 | C26 | C20 | coref-ident | TK activity,TK activity |
| R19 | C27 | C3 | coref-ident | LPS,lipopolysaccharide (LPS) |
pubmed-sentences-benchmark
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| S1 | 0-126 | Sentence | denotes | CD14-mediated translocation of nuclear factor-kappa B induced by lipopolysaccharide does not require tyrosine kinase activity. |
| S2 | 127-374 | Sentence | denotes | During the course of serious bacterial infections, lipopolysaccharide (LPS) is believed to interact with macrophage receptors, resulting in the generation of inflammatory mediators and systemic symptoms including hemodynamic instability and shock. |
| S3 | 375-467 | Sentence | denotes | CD14, a glycosylphosphatidylinositol-linked antigen, functions as an LPS signaling receptor. |
| S4 | 468-602 | Sentence | denotes | A critical issue concerns the mechanism by which CD14, which has no transmembrane domain, transduces its signal following LPS binding. |
| S5 | 603-798 | Sentence | denotes | Recently, investigators have hypothesized that CD14-mediated signaling is effected through a receptor-associated tyrosine kinase (TK), suggesting a multicomponent receptor model of LPS signaling. |
| S6 | 799-950 | Sentence | denotes | Wild-type Chinese hamster ovary (CHO)-K1 cells can be activated by endotoxin to release arachidonate following transfection with human CD14 (CHO/CD14). |
| S7 | 951-1052 | Sentence | denotes | Nuclear translocation of cytosolic NF-kappa B is correlated with a number of LPS-inducible responses. |
| S8 | 1053-1210 | Sentence | denotes | We sought to determine if this pathway were present in CHO/CD14 cells and to elucidate the relationship of NF-kappa B activation to the CD14 receptor system. |
| S9 | 1211-1350 | Sentence | denotes | LPS-stimulated translocation of NF-kappa B in CHO/CD14 cells resembled the same response in the murine macrophage-like cell line RAW 264.7. |
| S10 | 1351-1624 | Sentence | denotes | Protein synthesis inhibitors and corticosteroids, which suppress arachidonate release and the synthesis of proinflammatory cytokines, had no effect on translocation of NF-kappa B in CHO/CD14 or RAW 264.7 cells, demonstrating that NF-kappa B translocation is an early event. |
| S11 | 1625-1824 | Sentence | denotes | Although TK activity was consistently observed by immunoblotting extracts from activated RAW 264.7 cells, LPS-induced phosphotyrosine residues were not observed from similarly treated CHO/CD14 cells. |
| S12 | 1825-2044 | Sentence | denotes | Furthermore, the TK inhibitors herbimycin A and genistein failed to inhibit translocation of NF-kappa B in CHO/CD14 or RAW 264.7 cells, although both of these agents inhibited LPS-induced TK activity in RAW 264.7 cells. |
| S13 | 2045-2166 | Sentence | denotes | These results imply that TK activity is not obligatory for CD14-mediated signal transduction to occur in response to LPS. |
GENIAcorpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-4 | protein_molecule | denotes | CD14 |
| T2 | 31-53 | protein_molecule | denotes | nuclear factor-kappa B |
| T3 | 65-83 | lipid | denotes | lipopolysaccharide |
| T4 | 101-109 | amino_acid_monomer | denotes | tyrosine |
| T5 | 148-176 | other_name | denotes | serious bacterial infections |
| T6 | 178-196 | lipid | denotes | lipopolysaccharide |
| T7 | 198-201 | lipid | denotes | LPS |
| T8 | 232-252 | protein_family_or_group | denotes | macrophage receptors |
| T9 | 285-307 | other_name | denotes | inflammatory mediators |
| T10 | 340-363 | other_name | denotes | hemodynamic instability |
| T11 | 368-373 | other_name | denotes | shock |
| T12 | 375-379 | protein_molecule | denotes | CD14 |
| T13 | 383-426 | protein_family_or_group | denotes | glycosylphosphatidylinositol-linked antigen |
| T14 | 444-447 | lipid | denotes | LPS |
| T15 | 517-521 | protein_molecule | denotes | CD14 |
| T16 | 536-556 | protein_domain_or_region | denotes | transmembrane domain |
| T17 | 590-593 | lipid | denotes | LPS |
| T18 | 650-654 | protein_molecule | denotes | CD14 |
| T19 | 716-724 | amino_acid_monomer | denotes | tyrosine |
| T20 | 784-787 | lipid | denotes | LPS |
| T21 | 809-845 | cell_line | denotes | Chinese hamster ovary (CHO)-K1 cells |
| T22 | 887-899 | other_organic_compound | denotes | arachidonate |
| T23 | 934-938 | protein_molecule | denotes | CD14 |
| T24 | 940-944 | protein_molecule | denotes | CHO/ |
| T25 | 944-948 | protein_molecule | denotes | CD14 |
| T26 | 1028-1031 | lipid | denotes | LPS |
| T27 | 1108-1112 | cell_line | denotes | CHO/ |
| T28 | 1112-1116 | protein_molecule | denotes | CD14 |
| T29 | 1160-1170 | protein_molecule | denotes | NF-kappa B |
| T30 | 1189-1193 | protein_molecule | denotes | CD14 |
| T31 | 1211-1214 | lipid | denotes | LPS |
| T32 | 1243-1253 | protein_molecule | denotes | NF-kappa B |
| T33 | 1257-1261 | cell_line | denotes | CHO/ |
| T34 | 1261-1265 | protein_molecule | denotes | CD14 |
| T35 | 1307-1339 | cell_line | denotes | murine macrophage-like cell line |
| T36 | 1340-1349 | cell_line | denotes | RAW 264.7 |
| T37 | 1384-1399 | lipid | denotes | corticosteroids |
| T38 | 1416-1428 | other_organic_compound | denotes | arachidonate |
| T39 | 1458-1483 | protein_family_or_group | denotes | proinflammatory cytokines |
| T40 | 1519-1529 | protein_molecule | denotes | NF-kappa B |
| T41 | 1537-1541 | protein_molecule | denotes | CD14 |
| T42 | 1545-1560 | cell_line | denotes | RAW 264.7 cells |
| T43 | 1581-1591 | protein_molecule | denotes | NF-kappa B |
| T44 | 1634-1645 | other_name | denotes | TK activity |
| T45 | 1675-1698 | other_name | denotes | immunoblotting extracts |
| T46 | 1714-1729 | cell_line | denotes | RAW 264.7 cells |
| T47 | 1731-1767 | amino_acid_monomer | denotes | LPS-induced phosphotyrosine residues |
| T48 | 1809-1823 | cell_line | denotes | CHO/CD14 cells |
| T49 | 1842-1855 | other_name | denotes | TK inhibitors |
| T50 | 1856-1868 | other_organic_compound | denotes | herbimycin A |
| T51 | 1873-1882 | other_organic_compound | denotes | genistein |
| T52 | 1918-1928 | protein_molecule | denotes | NF-kappa B |
| T53 | 1932-1940 | cell_line | denotes | CHO/CD14 |
| T54 | 1944-1959 | cell_line | denotes | RAW 264.7 cells |
| T55 | 2001-2004 | lipid | denotes | LPS |
| T56 | 2013-2024 | other_name | denotes | TK activity |
| T57 | 2028-2043 | cell_line | denotes | RAW 264.7 cells |
| T58 | 2070-2081 | other_name | denotes | TK activity |
| T59 | 2104-2108 | protein_molecule | denotes | CD14 |
| T60 | 2162-2165 | lipid | denotes | LPS |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 368-373 | Phenotype | denotes | shock | HP:0031273 |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 156-176 | Disease | denotes | bacterial infections | http://purl.obolibrary.org/obo/MONDO_0005113 |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 809-824 | OrganismTaxon | denotes | Chinese hamster | 10029 |
| T2 | 928-933 | OrganismTaxon | denotes | human | 9606 |
Anatomy-UBERON
| Id | Subject | Object | Predicate | Lexical cue | uberon_id |
|---|---|---|---|---|---|
| T1 | 232-242 | Body_part | denotes | macrophage | http://purl.obolibrary.org/obo/CL_0000235 |
| T2 | 536-549 | Body_part | denotes | transmembrane | http://purl.obolibrary.org/obo/GO_0016020 |
| T3 | 825-830 | Body_part | denotes | ovary | http://purl.obolibrary.org/obo/UBERON_0000992 |
| T4 | 1314-1324 | Body_part | denotes | macrophage | http://purl.obolibrary.org/obo/CL_0000235 |
CL-cell
| Id | Subject | Object | Predicate | Lexical cue | cl_id |
|---|---|---|---|---|---|
| T1 | 232-242 | Cell | denotes | macrophage | http://purl.obolibrary.org/obo/CL:0000235|http://purl.obolibrary.org/obo/CL:0000394 |
| T3 | 1314-1324 | Cell | denotes | macrophage | http://purl.obolibrary.org/obo/CL:0000235|http://purl.obolibrary.org/obo/CL:0000394 |