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Negative regulation of the Apaf-1 apoptosome by Hsp70.
Saleh, A; Srinivasula, S M; Balkir, L; Robbins, P D; Alnemri, E S.
Affiliation
  • Saleh A; Center for Apoptosis Research and Department of Microbiology and Immunology, Kimmel Cancer Institute, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
Nat Cell Biol ; 2(8): 476-83, 2000 Aug.
Article in En | MEDLINE | ID: mdl-10934467
ABSTRACT
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.
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Collection: 01-internacional Database: MEDLINE Main subject: Proteins / Apoptosis / HSP70 Heat-Shock Proteins Limits: Humans Language: En Journal: Nat Cell Biol Year: 2000 Type: Article Affiliation country: United States
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Proteins / Apoptosis / HSP70 Heat-Shock Proteins Limits: Humans Language: En Journal: Nat Cell Biol Year: 2000 Type: Article Affiliation country: United States