Selective blockers of voltage-gated K+ channels depolarize human T lymphocytes: mechanism of the antiproliferative effect of charybdotoxin

Proc Natl Acad Sci U S A. 1992 Nov 1;89(21):10094-8. doi: 10.1073/pnas.89.21.10094.

Abstract

Charybdotoxin (ChTX), a K+ channel blocker, depolarizes human peripheral T lymphocytes and renders them insensitive to activation by mitogen. We observed four types of K+ channels in human T cells: one voltage-activated, and three Ca(2+)-activated. To discern the mechanism by which ChTX depolarizes T cells, we examined the sensitivity of both the voltage-activated and Ca(2+)-activated K+ channels to ChTX and other peptide channel blockers. All four types were blocked by ChTX, whereas noxiustoxin and margatoxin blocked only the voltage-activated channels. All three toxins, however, produced equivalent depolarization in human T cells. We conclude that the membrane potential of resting T cells is set by voltage-activated channels and that blockade of these channels is sufficient to depolarize resting human T cells and prevent activation.

MeSH terms

  • Calcium / pharmacology
  • Cells, Cultured
  • Charybdotoxin
  • Egtazic Acid / pharmacology
  • Electric Conductivity / drug effects
  • Humans
  • Ion Channel Gating / drug effects
  • Kinetics
  • Lymphocyte Activation / drug effects*
  • Membrane Potentials / drug effects
  • Neurotoxins / pharmacology*
  • Potassium Channels / drug effects
  • Potassium Channels / physiology*
  • Scorpion Venoms / pharmacology*
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology
  • T-Lymphocytes / physiology*
  • Time Factors

Substances

  • Neurotoxins
  • Potassium Channels
  • Scorpion Venoms
  • Charybdotoxin
  • Egtazic Acid
  • margatoxin
  • noxiustoxin
  • Calcium