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
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
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B-Lymphocytes / radiation effects*
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Benzoquinones
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Cell Line
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Cesium Radioisotopes
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Dose-Response Relationship, Radiation
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Enzyme Activation
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Gamma Rays
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Humans
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Inositol 1,4,5-Trisphosphate / metabolism*
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Isoquinolines / pharmacology
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Kinetics
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Lactams, Macrocyclic
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NF-kappa B / metabolism
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Phosphorylation
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Piperazines / pharmacology
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Protein Kinase C / metabolism*
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Protein Kinase C / radiation effects
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Protein-Tyrosine Kinases / antagonists & inhibitors
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Protein-Tyrosine Kinases / metabolism*
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Protein-Tyrosine Kinases / radiation effects
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Quinones / pharmacology
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Rifabutin / analogs & derivatives
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Signal Transduction / radiation effects*
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Tumor Cells, Cultured
Substances
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Benzoquinones
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Cesium Radioisotopes
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Isoquinolines
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Lactams, Macrocyclic
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NF-kappa B
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Piperazines
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Quinones
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Rifabutin
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herbimycin
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1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
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Inositol 1,4,5-Trisphosphate
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Protein-Tyrosine Kinases
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Protein Kinase C