Negative regulation of the Apaf-1 apoptosome by Hsp70

被引:684
作者
Saleh, A [1 ]
Srinivasula, SM
Balkir, L
Robbins, PD
Alnemri, ES
机构
[1] Thomas Jefferson Univ, Kimmel Canc Inst, Ctr Apoptosis Res, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Kimmel Canc Inst, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
[3] Univ Pittsburgh, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
关键词
D O I
10.1038/35019510
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Release of cytochrome c from mitochondria by apoptotic signals induces ATP/dATP-dependent formation of the oligomeric Apaf-1-caspase-9 apoptosome. Here we show that the documented anti-apoptotic effect of the principal heat-shock protein, Hsp70, is mediated through its direct association with the caspase-recruitment domain (CARD) of Apaf-1 and through inhibition of apoptosome formation. The interaction between Hsp70 and Apaf-1 prevents oligomerization of Apaf-1 and association of Apaf-1 with procaspase-9, On the basis of these results, we propose that resistance to apoptosis exhibited by stressed cells and some tumours, which constitutively express high levels of Hsp70, may be due in part to modulation of Apaf-1 function by Hsp70.
引用
收藏
页码:476 / 483
页数:8
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