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Article: c-Src mediates thrombin-induced NF-κB activation and IL-8/CXCL8 expression in lung epithelial cells
Title | c-Src mediates thrombin-induced NF-κB activation and IL-8/CXCL8 expression in lung epithelial cells |
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Authors | |
Issue Date | 2006 |
Citation | Journal of Immunology, 2006, v. 177, n. 5, p. 3427-3438 How to Cite? |
Abstract | In this study, we examined the regulation of NF-κB activation and IL-8/CXCL8 expression by thrombin in human lung epithelial cells (EC). Thrombin caused a concentration-dependent increase in IL-8/CXCL8 release in a human lung EC line (A549) and primary normal human bronchial EC. In A549 cells, thrombin, SFLLRN-NH2 (a protease-activated receptor 1 (PAR1) agonist peptide), and GYPGQV-NH2 (a PAR4 agonist peptide), but not TFRGAP-NH 2 (a PAR3 agonist peptide), induced an increase in IL-8/CXCL8-luciferase (Luc) activity. The thrombin-induced IL-8/CXCL8 release was attenuated by D-phenylalanyl-L-prolyl-L-arginine chloromethyl ketone (a thrombin inhibitor), U73122 (a phosphoinositide-phospholipase C inhibitor), Ro-32-0432 (a protein kinsase C α (PKCα) inhibitor), an NF-κB inhibitor peptide, and Bay 117082 (an IκB phosphorylation inhibitor). Thrombin-induced increase in IL-8/CXCL8-Luc activity was inhibited by the dominant-negative mutant of c-Src and the cells transfected with the κB site mutation of the IL-8/CXCL8 construct. Thrombin caused time-dependent increases in phosphorylation of c-Src at tyrosine 416 and c-Src activity. Thrombin-elicited c-Src activity was inhibited by Ro-32-0432. Stimulation of cells with thrombin activated IκB kinase αβ (IKKαβ), IκBα phosphorylation, IκBα degradation, p50 and p65 translocation from the cytosol to the nucleus, NF-κB-specific DNA-protein complex formation, and κB-Luc activity. Pretreatment of A549 cells with Ro-32-4032 and the dominant-negative mutant of c-Src DN inhibited thrombin-induced IKKαβ activity, κB-Luc activity, and NF-κB-specific DNA-protein complex formation. Further studies revealed that thrombin induced PKCα, c-Src, and IKKαβ complex formation. These results show for the first time that thrombin, acting through PAR1 and PAR4, activates the phosphoinositide-phospholipase C/PKCα/c-Src/ IKKαβ signaling pathway to induce NF-κB activation, which in turn induces IL-8/CXCL8 expression and release in human lung EC. Copyright © 2006 by The American Association of Immunologists, Inc. |
Persistent Identifier | http://hdl.handle.net/10722/241140 |
ISSN | 2023 Impact Factor: 3.6 2023 SCImago Journal Rankings: 1.558 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Lin, Chien Huang | - |
dc.contributor.author | Cheng, Hui Wen | - |
dc.contributor.author | Hsu, Ming Jen | - |
dc.contributor.author | Chen, Mei Chieh | - |
dc.contributor.author | Lin, Chia Chin | - |
dc.contributor.author | Chen, Bing Chang | - |
dc.date.accessioned | 2017-05-26T03:36:55Z | - |
dc.date.available | 2017-05-26T03:36:55Z | - |
dc.date.issued | 2006 | - |
dc.identifier.citation | Journal of Immunology, 2006, v. 177, n. 5, p. 3427-3438 | - |
dc.identifier.issn | 0022-1767 | - |
dc.identifier.uri | http://hdl.handle.net/10722/241140 | - |
dc.description.abstract | In this study, we examined the regulation of NF-κB activation and IL-8/CXCL8 expression by thrombin in human lung epithelial cells (EC). Thrombin caused a concentration-dependent increase in IL-8/CXCL8 release in a human lung EC line (A549) and primary normal human bronchial EC. In A549 cells, thrombin, SFLLRN-NH2 (a protease-activated receptor 1 (PAR1) agonist peptide), and GYPGQV-NH2 (a PAR4 agonist peptide), but not TFRGAP-NH 2 (a PAR3 agonist peptide), induced an increase in IL-8/CXCL8-luciferase (Luc) activity. The thrombin-induced IL-8/CXCL8 release was attenuated by D-phenylalanyl-L-prolyl-L-arginine chloromethyl ketone (a thrombin inhibitor), U73122 (a phosphoinositide-phospholipase C inhibitor), Ro-32-0432 (a protein kinsase C α (PKCα) inhibitor), an NF-κB inhibitor peptide, and Bay 117082 (an IκB phosphorylation inhibitor). Thrombin-induced increase in IL-8/CXCL8-Luc activity was inhibited by the dominant-negative mutant of c-Src and the cells transfected with the κB site mutation of the IL-8/CXCL8 construct. Thrombin caused time-dependent increases in phosphorylation of c-Src at tyrosine 416 and c-Src activity. Thrombin-elicited c-Src activity was inhibited by Ro-32-0432. Stimulation of cells with thrombin activated IκB kinase αβ (IKKαβ), IκBα phosphorylation, IκBα degradation, p50 and p65 translocation from the cytosol to the nucleus, NF-κB-specific DNA-protein complex formation, and κB-Luc activity. Pretreatment of A549 cells with Ro-32-4032 and the dominant-negative mutant of c-Src DN inhibited thrombin-induced IKKαβ activity, κB-Luc activity, and NF-κB-specific DNA-protein complex formation. Further studies revealed that thrombin induced PKCα, c-Src, and IKKαβ complex formation. These results show for the first time that thrombin, acting through PAR1 and PAR4, activates the phosphoinositide-phospholipase C/PKCα/c-Src/ IKKαβ signaling pathway to induce NF-κB activation, which in turn induces IL-8/CXCL8 expression and release in human lung EC. Copyright © 2006 by The American Association of Immunologists, Inc. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of Immunology | - |
dc.title | c-Src mediates thrombin-induced NF-κB activation and IL-8/CXCL8 expression in lung epithelial cells | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.pmid | 16920985 | - |
dc.identifier.scopus | eid_2-s2.0-33747760699 | - |
dc.identifier.volume | 177 | - |
dc.identifier.issue | 5 | - |
dc.identifier.spage | 3427 | - |
dc.identifier.epage | 3438 | - |
dc.identifier.isi | WOS:000240002800081 | - |
dc.identifier.issnl | 0022-1767 | - |