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Proliferation and Na+/H+ Exchange Activation by Endothelin in Vascular Smooth Muscle Cells
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1991
Year
Cardiovascular FunctionCell GrowthCellular PhysiologyInsulin SignalingOxidative StressAngiogenesisGrowth FactorNa+/h+ Exchange ActivationCell SignalingMolecular PhysiologyBiochemistryVascular AdaptationVascular BiologyEndocrinologyPharmacologyCell BiologySignal TransductionNatural SciencesPhysiologyEndothelial DysfunctionGrowth FactorsMetabolismMedicineSustained AlkalinizationExtracellular Matrix
Initiation and development of proliferative responses to growth factors are often associated to an activation of the Na+/H+ exchange. The present work examined the effect of endothelin (ET-1) on cell proliferation and Na+/H+ exchange in cultured vascular smooth muscle cells. In rat aortic vascular smooth muscle, ET-1 (0.1 to 10 nmol/L) increased the [3H] thymidine uptake in a dose-dependent manner. This effect was enhanced in presence of insulin (0.1 micrograms/mL to 10 micrograms/mL) as a function of concentration. The Na+/H+ exchange, which is a necessary response for mitogenesis, was dose-dependently stimulated by increasing concentrations of ET-1 (1 to 1000 nmol/L) and presented a biphasic response: a transient acidification followed by a sustained alkalinization. Alkalinization induced by ET-1 was similar to that obtained by the phorbol 12-myristate 13-acetate (PMA). An inhibitor of protein kinase C, H7, or a long-term pretreatment of cells with PMA for 24 h inhibited the effect of ET-1 and PMA on Na+/H+ exchange. These results confirm that ET-1 could act as a growth factor for vascular smooth muscle cells and suggest that its mode of action depends for a large part to protein kinase C activation.