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p38丝裂原活化蛋白激酶在转录后水平调节内皮细胞血管细胞黏附分子-1的表达。

p38 mitogen activated protein kinase regulates endothelial VCAM-1 expression at the post-transcriptional level.

作者信息

Pietersma A, Tilly B C, Gaestel M, de Jong N, Lee J C, Koster J F, Sluiter W

机构信息

Department of Biochemistry, Cardiovascular Research Institute (COEUR), Erasmus University Rotterdam, The Netherlands.

出版信息

Biochem Biophys Res Commun. 1997 Jan 3;230(1):44-8. doi: 10.1006/bbrc.1996.5886.

Abstract

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. TNFalpha increased the activity of the p38 substrate MAP kinase-activated-protein (MAPKAP) 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 TNFalpha-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 TNFalpha 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.

摘要

细胞因子肿瘤坏死因子(TNF)α被发现可刺激人脐静脉内皮细胞中的p38丝裂原活化蛋白(MAP)激酶信号级联反应。TNFα使p38底物丝裂原活化蛋白激酶激活的蛋白(MAPKAP)激酶2的活性以及小热休克蛋白Hsp27随后的磷酸化增加了约两到三倍。这种刺激几乎被特异性p38 MAP激酶抑制剂SB203580完全阻断。该抑制剂还抑制了TNFα诱导的内皮黏附分子血管细胞黏附分子(VCAM)-1的表面表达。相比之下,p38 MAP激酶的抑制对细胞间细胞黏附分子(ICAM)-1受刺激后的表面表达没有影响。SB203580不影响TNFα诱导的VCAM-1 mRNA积累,这表明p38 MAP激酶信号级联反应在转录后水平调节内皮细胞中VCAM-1的表达。

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