首页> 外文期刊>FEBS Letters >Tumour promotor 12‐O‐tetradecanoylphorbol 13‐acetate inhibits angiotensin II‐induced inositol phosphate production and cytosolic Ca2+ rise in rat renal mesangial cells
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Tumour promotor 12‐O‐tetradecanoylphorbol 13‐acetate inhibits angiotensin II‐induced inositol phosphate production and cytosolic Ca2+ rise in rat renal mesangial cells

机译:肿瘤启动子12-O-十四烷酰佛波醇13-乙酸盐抑制血管紧张素II诱导的大鼠肾小球系膜细胞中磷酸肌醇生成和胞质Ca2 +升高

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>Preincubation of rat renal mesangial cells with 12-O-tetradecanoylphorbol 13-acetate (TPA) strongly inhibited the increases of inositol phosphates and of free cytosolic Ca2+ induced by angiotensin II (10−7 M). TPA had no significant effect on the basal values of inositol phosphates and of free cytosolic Ca2+. Inhibition appeared already after 1 min and was maximal after 5 min. These effects occur without significant changes on angiotensin II binding in intact cells. The concentration of TPA needed (10−9–10−7 M) was in the range believed to cause specifically an activation of protein kinase C. Furthermore the biologically inactive phorbol ester 4α-phorbol 12,13-didecanoate was without effect. From the entirety of these results it is likely that protein kinase C inhibits angiotensin II activation of phospholipase C at a stage distal to receptor occupancy.
机译:>用12- O -十四烷酰佛波醇13-乙酸盐(TPA)预孵育大鼠肾系膜细胞强烈抑制肌醇磷酸酯和游离胞质Ca 2 + 诱导的升高通过血管紧张素II(10 −7 M)。 TPA对肌醇磷酸酯和游离胞质Ca 2 + 的基础值无显着影响。抑制作用在1分钟后已经出现,在5分钟后达到最大。这些作用在完整细胞中对血管紧张素II的结合没有明显改变的情况下发生。需要的TPA浓度(10 −9 –10 −7 M)在特定范围内,可以引起蛋白激酶C的活化。此外,佛波酯具有生物惰性4,α-佛波醇12,13-十二烷酸酯无效。从所有这些结果来看,蛋白激酶C可能在受体占据远端的阶段抑制了磷脂酶C的血管紧张素II活化。

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