Hsp27 negatively regulates cell death by interacting with cytochrome c

被引:829
作者
Bruey, JM
Ducasse, C
Bonniaud, P
Ravagnan, L
Susin, SA
Diaz-Latoud, C
Gurbuxani, S
Arrigo, AP
Kroemer, G
Solary, E
Garrido, C
机构
[1] INSERM, U517, Fac Med & Pharm, F-21033 Dijon, France
[2] CNRS, UMR 5534, Stress Lab, F-69622 Villeurbanne, France
[3] Inst Gustave Roussy, CNRS, UMR 1599, F-94805 Villejuif, France
关键词
D O I
10.1038/35023595
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mammalian cells respond to stress by accumulating or activating a set of highly conserved proteins known as heat-shock proteins (HSPs), Several of these proteins interfere negatively with apoptosis, We show that the small HSP known as Hsp27 inhibits cytochrome-c-mediated activation of caspases in the cytosol, Hsp27 does not interfere with granzyme-B-induced activation of caspases, nor with apoptosis-inducing factor-mediated, caspase-independent, nuclear changes. Hsp27 binds to cytochrome c released from the mitochondria to the cytosol and prevents cytochrome-c-mediated interaction of Apaf-1 with procaspase-9, Thus, Hsp27 interferes specifically with the mitochondrial pathway of caspase-dependent cell death.
引用
收藏
页码:645 / 652
页数:8
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