The voltage sensor of the mitochondrial permeability transition pore is tuned by the oxidation-reduction state of vicinal thiols. Increase of the gating potential by oxidants and its reversal by reducing agents

J Biol Chem. 1994 Jun 17;269(24):16638-42.

Abstract

Reaction of isolated mitochondria with a variety of agents that lead to oxidation or cross-linking of sulfhydryl groups leads to an increased "open" probability of the permeability transition pore, a cyclosporin A-sensitive channel. We have investigated the mechanism by which the pore is induced by menadione, diamide, arsenite, and tert-butylhydroperoxide. We find that these inducers increase the probability of pore opening by shifting its gating potential to higher values. Furthermore, the induced shift was prevented by treatment with N-ethylmaleimide or dithiothreitol. At moderate levels of depolarization an apparent I50 for N-ethylmaleimide of bout 5 microM can be defined, while the N-ethylmaleimide or dithiothreitol effects are overcome by maximal depolarization. We conclude that the oxidation-reduction state of vicinal thiols in cysteinyl residues plays a critical role in tuning the voltage sensor of the transition pore, with an increase of gating potential (i.e. an increase in the probability of pore opening despite a high transmembrane potential difference) as the couple is poised to a more oxidized state. These findings may have implications for the mechanism of cell damage under oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arsenites / pharmacology
  • Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone / pharmacology
  • Diamide / pharmacology
  • Dithiothreitol / pharmacology*
  • Ethylmaleimide / pharmacology*
  • Intracellular Membranes / drug effects
  • Intracellular Membranes / physiology*
  • Ion Channel Gating / drug effects
  • Ion Channels / drug effects
  • Ion Channels / physiology*
  • Kinetics
  • Membrane Potentials / drug effects*
  • Membrane Potentials / physiology
  • Membrane Proteins / drug effects
  • Membrane Proteins / physiology*
  • Mitochondria, Liver / drug effects
  • Mitochondria, Liver / physiology*
  • Oxidants / pharmacology*
  • Oxidation-Reduction
  • Peroxides / pharmacology
  • Porins*
  • Probability
  • Rats
  • Vitamin K / pharmacology
  • Voltage-Dependent Anion Channels
  • tert-Butylhydroperoxide

Substances

  • Arsenites
  • Ion Channels
  • Membrane Proteins
  • Oxidants
  • Peroxides
  • Porins
  • Voltage-Dependent Anion Channels
  • Diamide
  • Vitamin K
  • Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone
  • tert-Butylhydroperoxide
  • arsenite
  • Ethylmaleimide
  • Dithiothreitol