Rho-kinase mediates lysophosphatidic acid-induced IL-8 and MCP-1 production via p38 and JNK pathways in human endothelial cells

被引:47
|
作者
Shimada, Hideaki [1 ]
Rajagopalan, Lakshman E. [1 ]
机构
[1] Pfizer Inc, Pfizer Global Res & Dev, Inflammat Res Unit, St Louis, MO USA
关键词
Lysophosphatidic acid; Rho kinase; Endothelial cell; p38 MAP kinase; JNK; Chemokine; NF-kappa B p65; KAPPA-B ACTIVATION; RHEUMATOID-ARTHRITIS; GENE-EXPRESSION; C-JUN; RECEPTOR; PROTEIN; INFLAMMATION; INHIBITION; MIGRATION; PROMOTER;
D O I
10.1016/j.febslet.2010.04.064
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lysophosphatidic acid (LPA), an inflammatory mediator that is elevated in multiple inflammatory diseases, is a potent activator of Rho kinase (ROCK) signaling and of chemokine production in endothelial cells. In this study, LPA activated ROCK, p38, JNK and NF-kappa B pathways and induced interleukin-8 (IL-8) and monocyte chemotactic protein-1 (MCP-1) mRNA and protein expression in human endothelial cells. We mapped signaling events downstream of ROCK, driving chemokine production. In summary, MCP-1 production was partly regulated by ROCK acting upstream of p38 and JNK and mediated downstream by NF-kappa B. IL-8 production was largely driven by ROCK through p38 and JNK activation, but with no involvement of NF-kappa B. (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2827 / 2832
页数:6
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