Human natural killer cells express Na+ channels. A pharmacologic flow cytometric study

J Immunol. 1990 Mar 15;144(6):2365-70.

Abstract

Voltage-gated excitability of purified human NK cells was studied by using flow cytometry and the voltage-sensitive dye, oxonol. Highly purified human NK cells (CD16 = 95 +/- 1%) from normal volunteers were prepared by using a negative panning technique. The Na(+)-channel agonists batrachotoxin (BTX) (1 to 4 microM) and veratridine (Ver) (100 to 400 microM) depolarized a population of highly purified human NK cells as determined by flow cytometry. BTX and Ver responses were concentration-, time-, temperature-, and Na(+)-dependent. The Na+ channel antagonist tetrodotoxin (1 microM) blocked BTX and Ver responses. Ver (100 microM) produced significant inhibition of cytotoxicity when purified NK cells were incubated with K562 tumor target cells in a 4-h 51Cr release cytotoxicity assay. The effect was blocked by tetrodotoxin. These results strongly suggest presence of functional Na+ channels in NK cells. Activation of voltage-dependent Na+ channels depolarizes cells and reduces their in vitro cytotoxic function.

Publication types

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

MeSH terms

  • Batrachotoxins / pharmacology
  • Cell Separation
  • Cell Survival
  • Cytotoxicity, Immunologic / drug effects
  • Flow Cytometry
  • Humans
  • Immunity, Cellular / drug effects
  • In Vitro Techniques
  • Killer Cells, Natural / physiology*
  • Membrane Potentials / drug effects
  • Sodium Channels / drug effects
  • Sodium Channels / physiology*
  • Tetrodotoxin / pharmacology
  • Veratridine / pharmacology

Substances

  • Batrachotoxins
  • Sodium Channels
  • Tetrodotoxin
  • Veratridine