Halenda S P, Feinstein M B
Biochem Biophys Res Commun. 1984 Oct 30;124(2):507-13. doi: 10.1016/0006-291x(84)91583-3.
The tumor-promoting phorbol ester PMA increased the incorporation of 32P-phosphate into PIP (150%) and PIP2 (50%) in human platelets over the same range of concentrations that stimulate protein kinase C activity (i.e. 1-10 ng/ml). PMA also increased the total content of PIP (2.5-fold) and PIP2 (1.5-fold). The increase in 32P-PIP and 32P-PIP2 was 50% completed at 2 min after 10 ng/ml PMA, and was maximal by 20 min. The increase in PIP and PIP2 was accompanied by a fall of 32P-PI and PI mass over the same time period and concentration range of PMA, but no 32P-PA was formed, indicating that phosphoinositide hydrolysis by phospholipase C was not stimulated. Inhibition of phospholipase C activity by increasing platelet cyclic AMP did not duplicate the effects of PMA. We conclude that PMA may directly affect inositol lipid kinases and/or phosphatases, or that PMA stimulation of protein kinase C provides feedback regulation of the enzymes that determine the levels of polyphosphoinositides involved in transmembrane stimulus-response coupling.
促肿瘤佛波酯PMA在刺激蛋白激酶C活性的相同浓度范围内(即1 - 10 ng/ml),使人类血小板中32P - 磷酸盐掺入PIP(增加150%)和PIP2(增加50%)。PMA还使PIP的总含量增加了2.5倍,PIP2增加了1.5倍。在加入10 ng/ml PMA后2分钟,32P - PIP和32P - PIP2的增加完成了50%,20分钟时达到最大值。在相同的时间段和PMA浓度范围内,PIP和PIP2的增加伴随着32P - PI和PI质量的下降,但未形成32P - PA,这表明磷脂酶C介导的磷酸肌醇水解未被刺激。通过增加血小板环磷酸腺苷来抑制磷脂酶C活性并不能复制PMA的作用。我们得出结论,PMA可能直接影响肌醇脂质激酶和/或磷酸酶,或者PMA对蛋白激酶C的刺激为决定参与跨膜刺激 - 反应偶联的多磷酸肌醇水平的酶提供了反馈调节。