Lavie Y, Piterman O, Liscovitch M
Department of Hormone Research, Weizmann Institute of Science, Rehovot, Israel.
FEBS Lett. 1990 Dec 17;277(1-2):7-10. doi: 10.1016/0014-5793(90)80796-l.
Recent evidence indicates that a major fraction of diacylglycerol that is produced in hormonally stimulated cells arises by phosphatidylcholine hydrolysis via the sequential action of phospholipase D and phosphatidic acid phosphohydrolase (PAP). We have previously reported that sphingoid bases stimulate phospholipase D activity in NG108-15 cells. The evidence presented here demonstrates that in sphingosine-treated NG108-15 cells, elevated phosphatidic acid levels are accompanied by a parallel, time- and dose-dependent decrease in diacylglycerol levels. DL-propranolol, a known inhibitor of PAP, exerted similar effects, suggesting that the action of sphingosine may have been due to inhibition of PAP activity. This prediction was confirmed in in vitro experiments in which it was demonstrated that sphingosine is as potent an inhibitor of both cytosolic and membrane-associated PAP activity as propranolol. The hypothesis that sphingoid bases may exert a dual action in diacylglycerol signal termination is proposed.
最近的证据表明,在激素刺激的细胞中产生的大部分二酰基甘油是通过磷脂酶D和磷脂酸磷酸水解酶(PAP)的顺序作用,由磷脂酰胆碱水解产生的。我们之前报道过,鞘氨醇碱基可刺激NG108-15细胞中的磷脂酶D活性。此处提供的证据表明,在经鞘氨醇处理的NG108-15细胞中,磷脂酸水平升高的同时,二酰基甘油水平会出现平行的、时间和剂量依赖性的下降。DL-普萘洛尔是一种已知的PAP抑制剂,也产生了类似的效果,这表明鞘氨醇的作用可能是由于抑制了PAP活性。这一预测在体外实验中得到了证实,实验表明鞘氨醇与普萘洛尔一样,是胞质和膜相关PAP活性的有效抑制剂。本文提出了鞘氨醇碱基可能在二酰基甘油信号终止中发挥双重作用的假说。