P38 mitogen activated protein kinase regulates endothelial VCAM-1 expression at the post-transcriptional level

被引:187
作者
Pietersma, A
Tilly, BC
Gaestel, N
deJong, N
Lee, JC
Koster, JF
Sluiter, W
机构
[1] ERASMUS UNIV ROTTERDAM,DEPT BIOCHEM,INST CARDIOVASC RES,NL-3000 DR ROTTERDAM,NETHERLANDS
[2] MAX DELBRUCK CTR MOL MED,BERLIN,GERMANY
[3] SMITHKLINE BEECHAM PHARMACEUT,DEPT CELLULAR BIOCHEM,KING OF PRUSSIA,PA 19406
关键词
D O I
10.1006/bbrc.1996.5886
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
The cytokine tumor necrosis factor (TNF) alpha was found to stimulate the p38 mitogen activated protein (MAP) kinase signalling cascade in human umbilical vein endothelial cells. TNF alpha increased the activity of the p38 substrate MAP kinase-activated-protein (MAPK-KAP) kinase 2 and the subsequent phosphorylation of the small heat shock protein Hsp27 about two to three fold. This stimulation was blocked almost completely by the specific p38 MAP kinase inhibitor SB203580. This inhibitor also suppressed the TNF alpha-induced surface expression of the endothelial adhesion molecule vascular cell adhesion molecule (VCAM)-1. In contrast, inhibition of p38 MAP kinase had no effect on the stimulated surface expression of the intercellular cell adhesion molecule (ICAM)-1. VCAM-1 mRNA accumulation induced by TNF alpha was not affected by SB203580, suggesting that the p38 MAP kinase signalling cascade regulates the endothelial expression of VCAM-1 at the post-transcriptional level. (C) 1997 Academic Press
引用
收藏
页码:44 / 48
页数:5
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