Hsp27 negatively regulates cell death by interacting with cytochrome c

Nat Cell Biol. 2000 Sep;2(9):645-52. doi: 10.1038/35023595.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis Inducing Factor
  • Apoptosis*
  • Caspases / metabolism
  • Cytochrome c Group / metabolism*
  • Cytosol / metabolism
  • Cytosol / physiology
  • Enzyme Activation
  • Flavoproteins / metabolism
  • HSP27 Heat-Shock Proteins
  • Heat-Shock Proteins / metabolism*
  • Humans
  • Membrane Proteins / metabolism
  • Molecular Chaperones
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • U937 Cells

Substances

  • AIFM1 protein, human
  • Apoptosis Inducing Factor
  • Cytochrome c Group
  • Flavoproteins
  • HSP27 Heat-Shock Proteins
  • HSPB1 protein, human
  • Heat-Shock Proteins
  • Membrane Proteins
  • Molecular Chaperones
  • Neoplasm Proteins
  • Caspases