Activation of P-type calcium channel regulates a unique thapsigargin-sensitive calcium pool in embryonic motoneurons

Eur J Neurosci. 2004 Feb;19(4):977-82. doi: 10.1111/j.0953-816x.2004.03196.x.

Abstract

By regulating voltage-dependent Ca2+ influx and intracellular Ca2+ homeostasis, electrical activity plays a central role in motoneuron development. Dissociated cultures of purified embryonic rat motoneurons were used to explore the molecular mechanisms by which Ca2+ influx control [Ca2+]i transients in these neurons. Thapsigargin (250 nm) and cyclopiazonic acid (10 micro m), which deplete Ca2+ stores in the endoplasmic reticulum, decrease by 30% the depolarization-induced [Ca2+]i transients in motoneurons without affecting voltage-activated calcium currents. This thapsigargin-sensitive intracellular Ca2+ pool differs from other previous described Ca2+ stores that are sensitive to ryanodine or caffeine, inositol triphosphate, insulin and from mitochondrial Ca2+ pools. Thapsigargin affected the Cav2.1 P-type Ca2+ channel component of the depolarization-induced [Ca2+]i transient in motoneurons but spared [Ca2+]i transient induced by Cav1 L-type and Cav2.2 N-type Ca2+ channel components, suggesting a close functional relationship between Cav2.1 subunit and this unique thapsigargin-sensitive Ca2+ store. Altogether the present results demonstrate a new pathway, used by embryonic motoneurons, to regulate Ca2+ signalling through voltage-activated (Cav2.1) Ca2+ channels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Calcium Channels, P-Type / metabolism*
  • Cells, Cultured
  • Embryo, Mammalian
  • Female
  • Motor Neurons / drug effects*
  • Motor Neurons / metabolism
  • Pregnancy
  • Rats
  • Rats, Sprague-Dawley
  • Thapsigargin / pharmacology*

Substances

  • Calcium Channels, P-Type
  • Thapsigargin
  • Calcium