The protonophore CCCP induces mitochondrial permeability transition without cytochrome c release in human osteosarcoma cells

FEBS Lett. 2001 Aug 10;503(1):69-74. doi: 10.1016/s0014-5793(01)02693-x.

Abstract

Mitochondrial permeability transition (MPT) and cytochrome c redistribution from mitochondria are two events associated with apoptosis. We investigated whether an MPT event obligatorily leads to cytochrome c release in vivo. We have previously shown that treatment of human osteosarcoma cells with the protonophore m-chlorophenylhydrazone (CCCP) for 6 h induces MPT and mitochondrial swelling without significant cell death. Here we demonstrate that release of cytochrome c does not occur and the cells remain viable even after 72 h of treatment with CCCP. Bax is not mobilized to mitochondria under these conditions. However, subsequent exposure of CCCP-treated cells to etoposide or staurosporine for 48 h results in rapid cell death and cytochrome c release that is accompanied by Bax association with mitochondria, demonstrating competency of these mitochondria to release cytochrome c with additional triggers. Our findings suggest that MPT is not a sufficient condition, in itself, to effect cytochrome c release.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Neoplasms / enzymology*
  • Bone Neoplasms / pathology
  • Carbonyl Cyanide m-Chlorophenyl Hydrazone / pharmacology*
  • Cell Membrane Permeability / drug effects*
  • Cytochrome c Group / metabolism*
  • Humans
  • Immunohistochemistry
  • Mitochondria / drug effects*
  • Osteosarcoma / enzymology*
  • Osteosarcoma / pathology
  • Tumor Cells, Cultured

Substances

  • Cytochrome c Group
  • Carbonyl Cyanide m-Chlorophenyl Hydrazone