Ohtsuka T, Okamura N, Ishibashi S
Biochim Biophys Acta. 1986 Oct 10;888(3):332-7. doi: 10.1016/0167-4889(86)90233-8.
Two proteins (Mr 46,000, pI 6.4 and 7.0), the phosphorylation of which was increased by any of the membrane-perturbing agents in parallel with activation of NADPH oxidase in intact guinea-pig polymorphonuclear leukocytes in our previous study (Okamura, N., Ohashi, S., Nagahisa, N. and Ishibashi, S. (1984) Arch. Biochem. Biophys. 228, 270-277), were also phosphorylated in a cell-free system prepared from the leukocytes. The in vitro phosphorylation of these two proteins was stimulated by the addition of phosphatidylserine in the presence of higher concentrations of Ca2+ (300-500 microM). The phosphorylation was further increased when protein kinase C partially purified from guinea-pig brain was added to the system. At a low concentration of Ca2+ (about 10 microM), stimulation of the phosphorylation was not attained by phosphatidylserine alone but required the addition of diacylglycerol or phorbol myristate acetate. On the other hand, the increase in the phosphorylation was inhibited by H-7, an inhibitor for protein kinase C. These results indicate that protein kinase C is involved in the phosphorylation of the two proteins, which may be related to the superoxide anion production stimulated by various membrane-perturbing agents.
在我们之前的研究中(冈村,N.,大桥,S.,永久,N.和石桥,S.(1984年)《生物化学与生物物理学文献》228卷,270 - 277页),完整的豚鼠多形核白细胞中,两种蛋白质(分子量46,000,等电点6.4和7.0)的磷酸化作用会被任何一种膜扰动剂增强,同时伴有NADPH氧化酶的激活。在从白细胞制备的无细胞体系中,这两种蛋白质也发生了磷酸化。在较高浓度的Ca2 +(300 - 500微摩尔)存在时,添加磷脂酰丝氨酸可刺激这两种蛋白质的体外磷酸化。当加入从豚鼠脑部分纯化的蛋白激酶C时,磷酸化作用进一步增强。在低浓度的Ca2 +(约10微摩尔)时,仅磷脂酰丝氨酸不能刺激磷酸化,而是需要添加二酰基甘油或佛波醇肉豆蔻酸酯。另一方面,蛋白激酶C的抑制剂H - 7可抑制磷酸化作用的增强。这些结果表明,蛋白激酶C参与了这两种蛋白质的磷酸化,这可能与各种膜扰动剂刺激的超氧阴离子产生有关。