Survival pathways regulating the apoptosis induced by tumour necrosis factor-α in primary cultured bovine endothelial cells

被引:16
作者
Clermont, F
Adam, E
Dumont, JE
Robaye, B
机构
[1] Free Univ Brussels, Inst Rech Interdisciplinare Biol Humaine & Mol, Inst Biol & Med Mol, B-6041 Gosselies, Belgium
[2] Free Univ Brussels, Mol Virol Lab, Inst Biol & Med Mol, Serv Chim Biol, B-6041 Gosselies, Belgium
[3] Free Univ Brussels, Fac Med, Inst Interdisciplinaire Biol Humaine & Mol, B-1070 Brussels, Belgium
关键词
tumour necrosis factor; endothelial cells; cytoprotective pathways; apoptosis;
D O I
10.1016/S0898-6568(02)00145-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The aim of the present study was to identify biochemical pathways driving the resistance of endothelial cells to apoptosis induced by tumour necrosis factor-alpha (TNF). (1) Although nuclear factor-kappa B (NF-kappaB) was activated by TNF, its inhibition by MG-132 failed to sensitize these cells. (2) The activation of protein kinase C (PKC) by phorbol ester completely abolished the TNF-induced cell death. (3) The phosphatidylinositol 3-kinase (PI3K) inhibitor wortmannin (Wo) triggered apoptosis and enhanced the TNF-induced cell death. (4) The MEK inhibitor PD98059 did not affect the TNF-induced apoptotic process. (5) The p38 is activated by TNF and its inhibition by SB203580 sensitized the cells to TNF. This is correlated with the inhibition of phosphorylation of heat-shock protein of 27 kDa (HSP27). These results indicate that TNF activates NF-kappaB, which does not drive any anti-apoptotic response, and p38, which plays an anti-apoptotic function probably through HSP27 phosphorylation. Moreover, PKC and PI3K are involved in the control of survival pathways. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:539 / 546
页数:8
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