Phosphorylation by protein kinase C modulates agonist binding to striatal dopamine D2 receptors

Biochem Int. 1990 Nov;22(3):575-82.

Abstract

The effect of purified protein kinase C (PKC) on dopamine D2 receptor binding was studied. Saturation binding with [3H]spiperone was not affected. In competition experiments using agonists PKC-treated membranes showed a significant reduction in the proportion of high affinity sites, and the influence of GTP gamma S was abolished. These results suggest that PKC-dependent mechanisms can regulate the coupling between the dopamine D2 receptor and its G-protein.

MeSH terms

  • Animals
  • Binding, Competitive / physiology
  • Cattle
  • Corpus Striatum / metabolism*
  • Dopamine Agents / metabolism*
  • In Vitro Techniques
  • Phosphorylation
  • Protein Kinase C / isolation & purification
  • Protein Kinase C / metabolism*
  • Radioligand Assay
  • Receptors, Dopamine / metabolism*
  • Receptors, Dopamine D2

Substances

  • Dopamine Agents
  • Receptors, Dopamine
  • Receptors, Dopamine D2
  • Protein Kinase C