Protein kinase C-mediated serine phosphorylation directly activates Raf-1 in murine hematopoietic cells

J Biol Chem. 1994 Jan 14;269(2):1249-56.

Abstract

We have previously found that Raf-1, which is activated by hematopoietic growth factors in association with phosphorylation, is required for hematopoietic cell proliferation. Recently, 12-O-tetradecanoylphorbol 13-acetate has been found to mediate Raf-1 phosphorylation, suggesting that protein kinase C (PKC) may be involved in the Raf-1 activation mechanism(s). Since PKC can be activated by hematopoietic growth factors, it was investigated as a potential "Raf-1 kinase-kinase." Results demonstrate that bryostatin 1, a pharmacologic activator of PKC, induces activation of Raf-1 in FDC-P1 cells. PKC inhibitors H7 and staurosporine block both bryostatin 1- and interleukin-3-mediated Raf-1 phosphorylation and FDC-P1 cell proliferation. Additionally, an antisense c-raf oligodeoxyribonucleotide specifically inhibits bryostatin 1-mediated proliferation, indicating a necessary role for Raf-1 in PKC signaling. Purified PKC can phosphorylate Raf-1 serine residues to high stoichiometry in vitro. Comparative phosphopeptide maps localize two PKC phosphorylation sites to Raf-1 phosphopeptides isolated from hematopoietic growth factor- or bryostatin 1-stimulated cells. The sites of PKC-mediated Raf-1 phosphorylation are deduced to be Ser497 and Ser619. Furthermore, PKC-mediated serine phosphorylation is sufficient to activate the enzymatic function of Raf-1 in vitro. These findings demonstrate that activated PKC can promote hematopoietic cell growth by regulating the enzymatic activity of Raf-1 through direct serine phosphorylation.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Bryostatins
  • Cell Division
  • Enzyme Activation
  • Humans
  • In Vitro Techniques
  • Interleukin-3 / physiology
  • Lactones / pharmacology
  • Macrolides
  • Molecular Sequence Data
  • Oligonucleotides, Antisense
  • Peptide Mapping
  • Peptides / chemistry
  • Phosphorylation
  • Phosphoserine / metabolism
  • Protein Kinase C / physiology*
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-raf
  • Signal Transduction

Substances

  • Bryostatins
  • Interleukin-3
  • Lactones
  • Macrolides
  • Oligonucleotides, Antisense
  • Peptides
  • Proto-Oncogene Proteins
  • Phosphoserine
  • bryostatin 1
  • Proto-Oncogene Proteins c-raf
  • Protein Kinase C