Lavie Y, Liscovitch M
Department of Hormone Research, Weizmann Institute of Science, Rehovot, Israel.
J Biol Chem. 1990 Mar 5;265(7):3868-72.
Recent studies suggest that signal-dependent formation of phosphatidic acid by phospholipase D-catalyzed hydrolysis of phosphatidylcholine is a novel trans-membrane signaling pathway in mammalian cells. We here demonstrate that sphingosine, as well as some other long chain bases, activates phospholipase D in neural-derived NG108-15 cells. Sphingosine potently stimulated phosphatidic acid and, in the presence of ethanol, phosphatidylethanol formation. (Phosphatidylethanol is a nonphysiological phospholipid which is characteristically produced by phospholipase D in the presence of ethanol.) Elevated phosphatidic acid levels were accompanied by increased phosphatidylinositol and phosphatidylglycerol production and a decrease in diacylglycerol levels. Sphingosine stimulated phospholipase D activity in a time- and concentration-dependent manner. A long aliphatic chain and a free 2-amino group were important structural requirements for the activation of phospholipase D by sphingosine-related molecules. We propose that phospholipase D may constitute an important cellular target for sphingosine action under both physiological and pathological circumstances.
最近的研究表明,磷脂酶D催化磷脂酰胆碱水解产生的信号依赖性磷脂酸形成是哺乳动物细胞中的一种新型跨膜信号通路。我们在此证明,鞘氨醇以及其他一些长链碱基可激活神经源性NG108-15细胞中的磷脂酶D。鞘氨醇强烈刺激磷脂酸的产生,并且在乙醇存在的情况下,刺激磷脂酰乙醇的形成。(磷脂酰乙醇是一种非生理性磷脂,其特征是在乙醇存在下由磷脂酶D产生。)磷脂酸水平升高伴随着磷脂酰肌醇和磷脂酰甘油产量的增加以及二酰基甘油水平的降低。鞘氨醇以时间和浓度依赖性方式刺激磷脂酶D活性。长脂肪链和游离2-氨基是鞘氨醇相关分子激活磷脂酶D的重要结构要求。我们提出,在生理和病理情况下,磷脂酶D可能构成鞘氨醇作用的重要细胞靶点。