GRK3 mediates desensitization of CRF1 receptors: a potential mechanism regulating stress adaptation

Am J Physiol Regul Integr Comp Physiol. 2001 Apr;280(4):R935-46. doi: 10.1152/ajpregu.2001.280.4.R935.

Abstract

Potential G protein-coupled receptor kinase (GRK) and protein kinase A (PKA) mediation of homologous desensitization of corticotropin-releasing factor type 1 (CRF1) receptors was investigated in human retinoblastoma Y-79 cells. Inhibition of PKA activity by PKI(5-22) or H-89 failed to attenuate homologous desensitization of CRF1 receptors, and direct activation of PKA by forskolin or dibutyryl cAMP failed to desensitize CRF-induced cAMP accumulation. However, treatment of permeabilized Y-79 cells with heparin, a nonselective GRK inhibitor, reduced homologous desensitization of CRF1 receptors by approximately 35%. Furthermore, Y-79 cell uptake of a GRK3 antisense oligonucleotide (ODN), but not of a random or mismatched ODN, reduced GRK3 mRNA expression by approximately 50% without altering GRK2 mRNA expression and inhibited homologous desensitization of CRF1 receptors by approximately 55%. Finally, Y-79 cells transfected with a GRK3 antisense cDNA construct exhibited an approximately 50% reduction in GRK3 protein expression and an ~65% reduction in homologous desensitization of CRF1 receptors. We conclude that GRK3 contributes importantly to the homologous desensitization of CRF1 receptors in Y-79 cells, a brain-derived cell line.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Colforsin / pharmacology
  • Cyclic AMP-Dependent Protein Kinases / antagonists & inhibitors
  • Cyclic AMP-Dependent Protein Kinases / genetics
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • DNA, Antisense
  • Enzyme Inhibitors / pharmacology
  • Eye Neoplasms
  • G-Protein-Coupled Receptor Kinase 3
  • Gene Expression Regulation, Enzymologic / drug effects
  • Gene Expression Regulation, Enzymologic / physiology
  • Humans
  • Isoquinolines / pharmacology
  • Oligodeoxyribonucleotides, Antisense / pharmacology
  • Peptide Fragments / pharmacology
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • RNA, Messenger / genetics
  • Receptors, Corticotropin-Releasing Hormone / drug effects
  • Receptors, Corticotropin-Releasing Hormone / genetics
  • Receptors, Corticotropin-Releasing Hormone / physiology*
  • Recombinant Proteins / metabolism
  • Retinoblastoma
  • Sulfonamides*
  • Transcription, Genetic / drug effects
  • Transfection
  • Tumor Cells, Cultured
  • beta-Adrenergic Receptor Kinases

Substances

  • DNA, Antisense
  • Enzyme Inhibitors
  • Isoquinolines
  • Oligodeoxyribonucleotides, Antisense
  • Peptide Fragments
  • RNA, Messenger
  • Receptors, Corticotropin-Releasing Hormone
  • Recombinant Proteins
  • Sulfonamides
  • Colforsin
  • CRF receptor type 1
  • Protein Serine-Threonine Kinases
  • Cyclic AMP-Dependent Protein Kinases
  • G-Protein-Coupled Receptor Kinase 3
  • GRK3 protein, human
  • beta-Adrenergic Receptor Kinases
  • N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide