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Proc Natl Acad Sci U S A ; 90(1): 252-6, 1993 Jan 01.
Article in English | MEDLINE | ID: mdl-8419931

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.


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