Capacitative calcium entry is inhibited in vascular endothelial cells by disruption of cytoskeletal microfilaments

FEBS Lett. 1997 Feb 17;403(2):191-6. doi: 10.1016/s0014-5793(97)00051-3.

Abstract

The role of an intact cytoskeleton for store-operated ('capacitative') Ca2+ influx was investigated in single cultured vascular endothelial cells. Capacitative Ca2+ entry was measured as changes of cytoplasmic Ca2+ concentration ([Ca2+]i) induced by depletion of Ca2+ stores with thapsigargin. In cells pretreated with cytochalasin D, an agent that disrupts the microfilament network of the cytoskeleton, as confirmed with FITC-phalloidin staining, capacitative Ca2+ entry was inhibited. Cytochalasin D did not affect basal [Ca2+]i nor ATP-induced increases of [Ca2+]i, indicating that release of Ca2+ from intracellular stores through the inositol-phosphate pathway was intact. These results suggest that microfilaments are an integral part of the mechanism for capacitative Ca2+ entry. The necessity for an intact cytoskeleton favors a conformational coupling model for store-operated Ca2+ influx.

Publication types

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

MeSH terms

  • Adenosine Triphosphate / pharmacology
  • Animals
  • Calcium / metabolism*
  • Cattle
  • Cells, Cultured
  • Cytoskeleton / drug effects
  • Cytoskeleton / metabolism*
  • Cytoskeleton / ultrastructure
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / metabolism*
  • Endothelium, Vascular / ultrastructure
  • Ion Transport
  • Microscopy, Confocal

Substances

  • Adenosine Triphosphate
  • Calcium