Functional roles of gamma2, gamma3 and gamma4, three new Ca2+ channel subunits, in P/Q-type Ca2+ channel expressed in Xenopus oocytes

J Physiol. 2001 May 1;532(Pt 3):583-93. doi: 10.1111/j.1469-7793.2001.0583e.x.

Abstract

Stargazin or [gamma]2, the product of the gene mutated in the stargazer mouse, is a homologue of the [gamma]1 protein, an accessory subunit of the skeletal muscle L-type Ca2+ channel. [gamma]2 is selectively expressed in the brain, and considered to be a putative neuronal Ca2+ channel subunit based mainly on homology to [gamma]1. Two new members of the [gamma] family expressed in the brain have recently been identified: [gamma]3 and [gamma]4. We have co-expressed, in Xenopus oocytes, the human [gamma]2, [gamma]3 and [gamma]4 subunits with the P/Q-type (Ca(V)2.1) Ca2+ channel and different regulatory subunits ([alpha]2-[delta]; [beta]1, [beta]2, [beta]3 or [beta]4). Subcellular distribution of the [gamma] subunits confirmed their membrane localization. Ba2+ currents, recorded using two-electrode voltage clamp, showed that the effects of the [gamma] subunits on the electrophysiological properties of the channel are, most of the time, minor. However, a fraction of the oocytes expressing [beta] subunits displayed an unusual slow-inactivating Ba2+ current. Expression of both [beta] and [gamma] subunits increased the appearance of the slow-inactivating current. Our data support a role for the [gamma] subunit as a brain Ca2+ channel modulatory subunit and suggest that [beta] and [gamma] subunits are involved in a switch between two regulatory modes of the P/Q-type channel inactivation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Barium / pharmacokinetics
  • Calcium / metabolism
  • Calcium Channels, N-Type* / chemistry
  • Calcium Channels, N-Type* / genetics
  • Calcium Channels, N-Type* / metabolism
  • Cell Line
  • Female
  • Gene Expression / physiology
  • Humans
  • Ion Channel Gating / physiology*
  • Kidney / cytology
  • Kinetics
  • Oocytes / physiology
  • Patch-Clamp Techniques
  • Protein Structure, Tertiary
  • Transfection
  • Xenopus laevis

Substances

  • Calcium Channels, N-Type
  • voltage-dependent calcium channel (P-Q type)
  • Barium
  • Calcium