Tyrosine phosphorylation is a mandatory proximal step in radiation-induced activation of the protein kinase C signaling pathway in human B-lymphocyte precursors

Proc Natl Acad Sci U S A. 1993 Jan 1;90(1):252-6. doi: 10.1073/pnas.90.1.252.

Abstract

Ionizing radiation triggers a signal in human B-lymphocyte precursors that is intimately linked to an active protein-tyrosine kinase regulatory pathway. We show that in B-lymphocyte precursors, irradiation with gamma-rays leads to (i) stimulation of phosphatidylinositol turnover; (ii) downstream activation by covalent modification of multiple serine-specific protein kinases, including protein kinase C; and (iii) activation of nuclear factor kappa B. All of the radiation-induced signals were effectively prevented by the protein-tyrosine kinase inhibitors genistein and herbimycin A. Thus, tyrosine phosphorylation is an important and perhaps mandatory proximal step in the activation of the protein kinase C signaling cascade in human B-lymphocyte precursors. Our report expands current knowledge of the radiation-induced signaling cascade by clarifying the chronological sequence of biochemical events that follow irradiation.

Publication types

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

MeSH terms

  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
  • B-Lymphocytes / radiation effects*
  • Benzoquinones
  • Cell Line
  • Cesium Radioisotopes
  • Dose-Response Relationship, Radiation
  • Enzyme Activation
  • Gamma Rays
  • Humans
  • Inositol 1,4,5-Trisphosphate / metabolism*
  • Isoquinolines / pharmacology
  • Kinetics
  • Lactams, Macrocyclic
  • NF-kappa B / metabolism
  • Phosphorylation
  • Piperazines / pharmacology
  • Protein Kinase C / metabolism*
  • Protein Kinase C / radiation effects
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Protein-Tyrosine Kinases / metabolism*
  • Protein-Tyrosine Kinases / radiation effects
  • Quinones / pharmacology
  • Rifabutin / analogs & derivatives
  • Signal Transduction / radiation effects*
  • Tumor Cells, Cultured

Substances

  • Benzoquinones
  • Cesium Radioisotopes
  • Isoquinolines
  • Lactams, Macrocyclic
  • NF-kappa B
  • Piperazines
  • Quinones
  • Rifabutin
  • herbimycin
  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
  • Inositol 1,4,5-Trisphosphate
  • Protein-Tyrosine Kinases
  • Protein Kinase C