Do submaximal InsP3 concentrations only induce the partial discharge of permeabilized hepatocyte calcium pools because of the concomitant reduction of intraluminal Ca2+ concentration?

FEBS Lett. 1992 Apr 27;301(3):287-90. doi: 10.1016/0014-5793(92)80258-i.

Abstract

In several types of cells whose cytoplasmic Ca2+ is regulated by inositol phosphate derivatives, low concentrations of InsP3 added to permeabilized cell suspensions induce the rapid discharge of part of the InsPs-sensitive Ca2+ pool instead of slow monophasic release of Ca2+ from the entire pool. As a tentative explanation for this puzzling observation, sometimes called 'quantal release', it was suggested that the reduced intraluminal Ca2+ concentration remaining in the Ca2+ pool after a certain amount of Ca2+ had been released might allosterically reduce the channels' affinity for InsP3 and the corresponding InsP3-dependent Ca2+ efflux, and thus result in partial pool discharge (Irvine, R.F. (1990) FEBS Lett. 263, 5-9). We have tested this hypothesis by manipulating the Ca2+ pool contents with ionophore, and found that the rate of InsP3-dependent Ca2+ efflux after ionophore-induced partial discharge of the Ca2+ pools was much faster than what was predicted on the basis of this hypothesis. Heterogeneity of the Ca2+ pools appears to be a more likely reason for the 'quantal release' behavior.

MeSH terms

  • Animals
  • Biological Transport
  • Calcium / metabolism*
  • Cations, Divalent
  • Cells, Cultured
  • Inositol 1,4,5-Trisphosphate / metabolism*
  • Ionomycin / pharmacology
  • Liver / cytology
  • Liver / drug effects
  • Liver / metabolism*
  • Rats

Substances

  • Cations, Divalent
  • Ionomycin
  • Inositol 1,4,5-Trisphosphate
  • Calcium