Oxidative modification of caspase-9 facilitates its activation via disulfide-mediated interaction with Apaf-1

Cell Res. 2009 Apr;19(4):449-57. doi: 10.1038/cr.2009.19.

Abstract

Intracellular reactive oxygen species (ROS) are known to regulate apoptosis. Activation of caspase-9, the initial caspase in the mitochondrial apoptotic cascade, is closely associated with ROS, but it is unclear whether ROS regulate caspase-9 via direct oxidative modification. The present study aims to elucidate the molecular mechanisms by which ROS mediate caspase-9 activation. Our results show that the cellular oxidative state facilitates caspase-9 activation. Hydrogen peroxide treatment causes the activation of caspase-9 and apoptosis, and promotes an interaction between caspase-9 and apoptotic protease-activating factor 1 (Apaf-1) via disulfide formation. In addition, in an in vitro mitochondria-free system, the thiol-oxidant diamide promotes auto-cleavage of caspase-9 and the caspase-9/Apaf-1 interaction by facilitating the formation of disulfide-linked complexes. Finally, a point mutation at C403 of caspase-9 impairs both H(2)O(2)-promoted caspase-9 activation and interaction with Apaf-1 through the abolition of disulfide formation. The association between cytochrome c and the C403S mutant is significantly weaker than that between cytochrome c and wild-type caspase-9, indicating that oxidative modification of caspase-9 contributes to apoptosome formation under oxidative stress. Taken together, oxidative modification of caspase-9 by ROS can mediate its interaction with Apaf-1, and can thus promote its auto-cleavage and activation. This mechanism may facilitate apoptosome formation and caspase-9 activation under oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Apoptosis
  • Apoptotic Protease-Activating Factor 1 / metabolism*
  • Caspase 9 / metabolism*
  • Cell Line
  • Cytochromes c / metabolism
  • Diamide / pharmacology
  • Disulfides / metabolism*
  • HeLa Cells
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Mutant Proteins / metabolism
  • Oxidative Stress*
  • Reactive Oxygen Species / metabolism
  • Reactive Oxygen Species / pharmacology

Substances

  • Apoptotic Protease-Activating Factor 1
  • Disulfides
  • Mutant Proteins
  • Reactive Oxygen Species
  • Diamide
  • Cytochromes c
  • Hydrogen Peroxide
  • Caspase 9