Voltage-dependent InsP3-insensitive calcium channels in membranes of pancreatic endoplasmic reticulum vesicles

Nature. 1990 Jul 26;346(6282):374-6. doi: 10.1038/346374a0.

Abstract

Stimulus-secretion coupling in exocrine glands involves Ca2+ release from intracellular stores. In endoplasmic reticulum vesicle preparations from rat exocrine pancreas, an inositol 1,4,5-trisphosphate(InsP3)-sensitive, as well as an InsP3-insensitive, Ca2+ pool has been characterized. But Ca2+ channels in the endoplasmic reticulum of rat exocrine pancreas have not been demonstrated at the level of single-channel current. We have now used the patch-clamp technique on endoplasmic reticulum vesicles fused by means of the dehydration-rehydration method. In excised patches, single Ba2(+)- and Ca2(+)-selective channels were recorded. The channel activity was markedly voltage-dependent. Caffeine increased channel open-state probability, whereas ruthenium red and Cd2+ blocked single-channel currents. Ryanodine, nifedipine and heparin had no effect on channel activity. The channel activity was not dependent on the free Ca2+ concentration, the presence of InsP3, or pH. We conclude that this calcium channel mediates Ca2+ release from an intracellular store through an InsP3-insensitive mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cadmium / pharmacology
  • Caffeine / pharmacology
  • Calcium Channels / drug effects
  • Calcium Channels / physiology*
  • Endoplasmic Reticulum / drug effects
  • Endoplasmic Reticulum / physiology*
  • Inositol 1,4,5-Trisphosphate / pharmacology*
  • Membrane Fusion
  • Membrane Potentials / drug effects
  • Nickel / pharmacology
  • Pancreas / physiology*
  • Rats
  • Ruthenium Red / pharmacology

Substances

  • Calcium Channels
  • Cadmium
  • Ruthenium Red
  • Caffeine
  • Nickel
  • Inositol 1,4,5-Trisphosphate