Pfeilschifter J
FEBS Lett. 1986 Jul 28;203(2):262-6. doi: 10.1016/0014-5793(86)80755-4.
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 4 alpha-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.
用12 - O -十四烷酰佛波醇-13 -乙酸酯(TPA)预孵育大鼠肾系膜细胞,可强烈抑制血管紧张素II(10⁻⁷ M)诱导的肌醇磷酸和游离胞质Ca²⁺的增加。TPA对肌醇磷酸和游离胞质Ca²⁺的基础值无显著影响。抑制作用在1分钟后即出现,5分钟后达到最大。这些效应出现时,完整细胞中血管紧张素II的结合无明显变化。所需TPA的浓度(10⁻⁹ - 10⁻⁷ M)在被认为能特异性激活蛋白激酶C的范围内。此外,无生物学活性的佛波醇酯4α -佛波醇12,13 -二癸酸酯没有作用。从所有这些结果来看,蛋白激酶C可能在受体占据后的一个远端阶段抑制血管紧张素II对磷脂酶C的激活。