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• W2089033249 abstract "To investigate the role of intracellular Ca2+ in the mechanism of cellular proliferation of vascular smooth muscle cells (VSMC), the effects of Ca2+-antagonists and calmodulin (CaM) inhibitors on DNA synthesis stimulated by serum-derived growth factors were studied in cultured VSMCs derived from rat aorta. DNA synthesis assessed by incorporation of [3H]thymidine into the cells was significantly stimulated by epidermal growth factor (EGF), platelet-derived growth factor (PDGF) or fetal bovine serum (FBS), of which the effects were dose-dependently inhibited by a variety of Ca2+-antagonists, such as verapamil, diltiazem and nicardipine. Trifluoperazine and W-7, both specific CaM inhibitors, similarly inhibited DNA synthesis stimulated by EGF, PDGF or FBS in a dose-dependent manner, whereas W-5, a less specific CaM inhibitor, was minimally effective. These data suggest that the Ca2+-CaM system plays an important role in the mechanism of growth factor-induced DNA synthesis in VSMCs." @default.
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• W2089033249 date "1987-01-01" @default.
• W2089033249 modified "2023-10-03" @default.
• W2089033249 title "Effects of Calcium-Antagonists and Calmodulin Inhibitors on DNA Synthesis in Cultured Rat Vascular Smooth Muscle Cells" @default.
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• W2089033249 doi "https://doi.org/10.1507/endocrj1954.34.313" @default.
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