Biswas P, Abboud H E, Kiyomoto H, Wenzel U O, Grandaliano G, Choudhury G G
Department of Medicine, University of Texas Health Science Center at San Antonio 78284, USA.
FEBS Lett. 1995 Oct 9;373(2):146-50. doi: 10.1016/0014-5793(95)01025-a.
Thrombin is a potent mitogen for mesangial cells and stimulates PDGF B-chain gene expression in these cells. It also activates phospholipase C (PLC) resulting in an increase in cytosolic Ca2+ and diacylglycerol (DAG) that are the physiological activators of protein kinase C (PKC). Immunoprecipitation of specific PKC isotypes from thrombin-stimulated mesangial cells with subsequent measurement of their enzymatic activity shows activation of Ca(2+)-dependent PKC alpha and Ca(2+)-independent PKC zeta in a time dependent manner. Optimum activation of both of these isozymes was obtained at 60 minutes. PKC alpha activity increased 83% over basal while activity of PKC zeta increased 104%. Prolonged exposure of mesangial cells to phorbol myristate acetic acid (PMA) inhibited the enzymatic activity of PKC alpha but not PKC zeta. This inhibition of PKC alpha had no effect on thrombin-induced DNA synthesis but abolished PDGF B-chain gene expression induced by thrombin. These data provide the first evidence that PKC alpha activation is necessary for thrombin-induced PDGF B-chain gene expression but not for thrombin-induced DNA synthesis.
凝血酶是系膜细胞的一种强效促有丝分裂原,可刺激这些细胞中血小板衍生生长因子B链(PDGF B-chain)基因的表达。它还能激活磷脂酶C(PLC),导致胞质Ca2+和二酰基甘油(DAG)增加,而它们是蛋白激酶C(PKC)的生理性激活剂。从凝血酶刺激的系膜细胞中免疫沉淀特定的PKC同工型,随后测量其酶活性,结果显示Ca2+依赖性PKCα和Ca2+非依赖性PKCζ呈时间依赖性激活。在60分钟时这两种同工酶均获得最佳激活。PKCα的活性比基础活性增加了83%,而PKCζ的活性增加了104%。系膜细胞长时间暴露于佛波醇肉豆蔻酸乙酸酯(PMA)会抑制PKCα的酶活性,但不影响PKCζ的酶活性。这种对PKCα的抑制对凝血酶诱导的DNA合成没有影响,但消除了凝血酶诱导的PDGF B链基因表达。这些数据首次证明,PKCα的激活对于凝血酶诱导的PDGF B链基因表达是必需的,但对于凝血酶诱导的DNA合成则不是必需的。