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  • 1
    Publication Date: 1990-03-02
    Description: Several immunologically distinct isozymes of inositol phospholipid-specific phospholipase C (PLC) have been purified from bovine brain. Murine NIH 3T3 fibroblasts were found to express PLC-gamma, but the expression of PLC-beta was barely detectable by radioimmunoassay or protein immunoblot. A mixture of monoclonal antibodies was identified that neutralizes the biological activity of both endogenous and injected purified PLC-gamma. When co-injected with oncogenic Ras protein or PLC-gamma, this mixture of antibodies inhibited the induction of DNA synthesis that characteristically results from the injection of these proteins into quiescent 3T3 cells. However, when oncogenic Ras protein or PLC-gamma was co-injected with a neutralizing monoclonal antibody to Ras, only the DNA synthesis induced by the Ras protein was inhibited--that induced by PLC was unaffected. These results suggest that the Ras protein is an upstream effector of PLC activity in phosphoinositide-specific signal transduction and that PLC-gamma activity is necessary for Ras-mediated induction of DNA synthesis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Smith, M R -- Liu, Y L -- Kim, H -- Rhee, S G -- Kung, H F -- N01-CO-74102/CO/NCI NIH HHS/ -- New York, N.Y. -- Science. 1990 Mar 2;247(4946):1074-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Biological Carcinogenesis and Development Program, National Cancer Institute-Frederick Cancer Research Facility, MD 21701.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2408147" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antibodies, Monoclonal/immunology ; Cell Line ; DNA/*biosynthesis ; Fibroblasts ; Growth Substances/pharmacology ; Hybridomas ; Immunoblotting ; Interphase ; Isoenzymes/immunology/*metabolism ; Microinjections ; Oncogene Protein p21(ras)/immunology/*pharmacology ; Radioimmunoassay ; Signal Transduction ; Type C Phospholipases/immunology/*metabolism/pharmacology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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