Thapsigargin inhibits Ca2+ entry into human neutrophil granulocytes

Biochem J. 1995 Jan 15;305 ( Pt 2)(Pt 2):525-8. doi: 10.1042/bj3050525.

Abstract

The mechanism of Ca2+ entry after ligand binding to receptors on the surface of non-excitable cells is a current focus of interest. Considerable attention has been given to Ca2+ influx induced by emptying of intracellular pools. Thapsigargin, an inhibitor of microsomal Ca(2+)-ATPase, is an important tool in inducing store-regulated Ca2+ influx. In the present paper we show that, at concentrations above 500 nM, thapsigargin also has an opposite effect: it inhibits store-regulated Ca2+ influx into Fura-2-loaded human neutrophil granulocytes. As thapsigargin has been frequently applied at concentrations up to 2 microM, its inhibitory action on plasma-membrane Ca2+ fluxes deserves consideration.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Transport
  • Calcium / metabolism*
  • Dose-Response Relationship, Drug
  • Humans
  • Neutrophils / drug effects
  • Neutrophils / metabolism*
  • Phosphorylation
  • Terpenes / pharmacology*
  • Tetradecanoylphorbol Acetate / pharmacology
  • Thapsigargin

Substances

  • Terpenes
  • Thapsigargin
  • Tetradecanoylphorbol Acetate
  • Calcium