The lipid connection-regulation of voltage-gated Ca(2+) channels by phosphoinositides

Pflugers Arch. 2007 Oct;455(1):147-55. doi: 10.1007/s00424-007-0272-9. Epub 2007 May 31.

Abstract

Recent findings have revealed a pivotal role for phospholipids phosphatidylinositol -4,5-biphosphate (PIP(2)) and phosphatidylinositol -3,4,5-trisphosphate (PIP(3)) in the regulation of high voltage-activated (HVA) Ca(2+) channels. PIP(2) exerts two opposing actions on HVA Ca(2+) channels: It stabilizes their activity but also produces a voltage-dependent inhibition that can be antagonized by protein kinase A (PKA) phosphorylation. PIP(2) depletion and arachidonic acid together mediate the slow, voltage-independent inhibition of HVA Ca(2+) channels by G( q/11 )-coupled receptors in neurons. A sufficient level of plasma membrane PIP(2) also appears to be necessary for G( betagamma )-mediated inhibition. On the other hand, increased production of PIP(3) by PI-3 kinases promotes trafficking of HVA Ca(2+) channels to the plasma membrane. This review discusses these findings and their implications.

Publication types

  • Review

MeSH terms

  • Animals
  • Arachidonic Acid / pharmacology
  • Calcium Channels / drug effects*
  • Humans
  • Ion Channel Gating / drug effects*
  • Lipids / chemistry
  • Lipids / physiology*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphatidylinositol 4,5-Diphosphate / pharmacology*
  • Phosphatidylinositols / pharmacology*
  • Second Messenger Systems / drug effects

Substances

  • Calcium Channels
  • Lipids
  • Phosphatidylinositol 4,5-Diphosphate
  • Phosphatidylinositols
  • Arachidonic Acid
  • Phosphatidylinositol 3-Kinases