The superoxide-generating NADPH oxidase of human neutrophils is electrogenic and associated with an H+ channel

Biochem J. 1987 Sep 1;246(2):325-9. doi: 10.1042/bj2460325.

Abstract

The membrane potential of cytoplasts, derived from human neutrophils, was depolarized by the activation of the superoxide-generating NADPH-dependent oxidase. The extent of the depolarization was inhibited by diphenylene iodonium and was therefore due directly to the activity of the oxidase, which must be electrogenic. The extent of the depolarization was influenced by alteration of the delta pH across the cytoplast membrane, indicating that the outward translocation of H+ eventually compensates for superoxide generation. The depolarization of the potential is enhanced by Cd2+, a blocker of H+ currents, suggesting that the compensatory movement is via an H+ channel.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Transport / drug effects
  • Humans
  • Hydrogen-Ion Concentration
  • In Vitro Techniques
  • Membrane Potentials
  • NADH, NADPH Oxidoreductases / blood*
  • NADPH Oxidases*
  • Neutrophils / metabolism*
  • Onium Compounds / pharmacology
  • Protons
  • Superoxides / metabolism
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • Onium Compounds
  • Protons
  • Superoxides
  • diphenyleneiodonium
  • NADH, NADPH Oxidoreductases
  • NADPH Oxidases
  • superoxide-forming enzyme
  • Tetradecanoylphorbol Acetate