ARC inhibits cytochrome c release from mitochondria and protects against hypoxia-induced apoptosis in heart-derived H9c2 cells

Circ Res. 1999 Dec 9;85(12):e70-7. doi: 10.1161/01.res.85.12.e70.

Abstract

Ischemia induces apoptosis as well as necrosis of cardiac myocytes. We recently reported the cloning of a cDNA that encodes an apoptotic inhibitor, ARC, that is expressed predominantly in cardiac and skeletal muscle. In the present study, we examined the ability of ARC to protect rat embryonic heart-derived H9c2 cells from apoptosis induced by hypoxia, a component of ischemia. We found that H9c2 cells express ARC and that exposure to hypoxia substantially reduces ARC expression while inducing apoptosis. Transfected H9c2 cells in which cytosolic ARC protein levels remain elevated during hypoxia were significantly more resistant to hypoxia-induced apoptosis than parental H9c2 cells or H9c2 cells transfected with a control vector. Loss of endogenous ARC in the cytosol of H9c2 cells was associated with translocation of ARC from the cytosol to intracellular membranes, release of cytochrome c from the mitochondria, activation of caspase-3, poly(ADP-ribose)polymerase (PARP) cleavage, and DNA fragmentation. All of these events were inhibited in H9c2 cells overexpressing ARC when compared with control cells. In contrast, caspase inhibitors prevented PARP cleavage but not cytochrome c release, suggesting that exogenously expressed ARC acts upstream of caspase activation in this model of apoptosis. These results demonstrate that ARC can protect heart myogenic H9c2 cells from hypoxia-induced apoptosis, and that ARC prevents cytochrome c release by acting upstream of caspase activation, perhaps at the mitochondrial level.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Animals, Newborn
  • Apoptosis Regulatory Proteins
  • Apoptosis* / genetics
  • Caspase 3
  • Caspases / metabolism
  • Cell Hypoxia / genetics
  • Cell Line
  • Cysteine Proteinase Inhibitors / biosynthesis*
  • Cytochrome c Group / metabolism*
  • DNA Fragmentation
  • Enzyme Activation / genetics
  • Fluorescent Antibody Technique, Indirect
  • Immunoblotting
  • Mitochondria / metabolism
  • Muscle Proteins / biosynthesis*
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Poly(ADP-ribose) Polymerases / metabolism
  • Rats
  • Transfection

Substances

  • Apoptosis Regulatory Proteins
  • Cysteine Proteinase Inhibitors
  • Cytochrome c Group
  • Muscle Proteins
  • Nol3 protein, rat
  • Poly(ADP-ribose) Polymerases
  • Casp3 protein, rat
  • Caspase 3
  • Caspases