The gastrin-releasing peptide receptor is rapidly phosphorylated by a kinase other than protein kinase C after exposure to agonist

J Biol Chem. 1995 Apr 7;270(14):8217-24. doi: 10.1074/jbc.270.14.8217.

Abstract

Several guanine nucleotide-binding protein-coupled receptors are known to be rapidly phosphorylated after agonist exposure. In this study we show that the gastrin-releasing peptide receptor (GRP-R) is rapidly phosphorylated in response to agonist exposure. When [32P]orthophosphate-labeled cells were exposed to bombesin, the receptor was maximally phosphorylated on serine and threonine residues within 1 min. Although addition of 12-O-tetradecanoylphorbol 13-acetate also resulted in phosphorylation of the GRP-R, elimination of protein kinase C activity using the inhibitor 7-hydroxystaurosporine did not prevent bombesin-induced GRP-R phosphorylation. We conclude that a kinase other than protein kinase C is principally responsible for the rapid, agonist-induced phosphorylation of the GRP-R.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Bombesin / pharmacology
  • Cells, Cultured
  • Enzyme Activation
  • Immune Sera
  • Mice
  • Mice, Inbred BALB C
  • Molecular Sequence Data
  • Phosphorylation
  • Protein Kinase C / metabolism*
  • Protein Kinases / metabolism*
  • Receptors, Bombesin / agonists
  • Receptors, Bombesin / immunology
  • Receptors, Bombesin / metabolism*
  • Tetradecanoylphorbol Acetate / pharmacology
  • Transfection

Substances

  • Immune Sera
  • Receptors, Bombesin
  • Protein Kinases
  • Protein Kinase C
  • Tetradecanoylphorbol Acetate
  • Bombesin