Liscovitch M
Department of Hormone Research, Weizmann Institute of Science, Rehovot, Israel.
J Biol Chem. 1989 Jan 25;264(3):1450-6.
12-O-Tetradecanoylphorbol-13-acetate (TPA) stimulates the release of free choline from intact NG108-15 cells into the medium, without affecting the release of phosphocholine (Liscovitch, M., Blusztajn, J.K., Freese, A., and Wurtman, R.J. (1987) Biochem. J. 241, 81-86). To test the hypothesis that this response reflects activation of cellular phospholipase D, via protein kinase C (Ca2+/phospholipid-dependent enzyme), I examined in NG108-15 cells the biosynthesis of the abnormal phospholipid phosphatidylethanol, produced by phospholipase D in the presence of ethanol by transphosphatidylation. Phosphatidylethanol production was quantitated by measuring the incorporation of phosphatidyl moieties (prelabeled metabolically with [3H]oleic acid) into phosphatidylethanol. The production of phosphatidylethanol in NG108-15 cells was virtually dependent on stimulation by TPA, in a time- and concentration-dependent manner (EC50 = 18 nM). The rate of 3H-phosphatidylethanol formation reached a peak after 10 min of incubation with TPA and declined gradually thereafter. The levels of 3H-phosphatidylethanol in TPA-treated cells were directly related to ethanol concentration in the physiologically attainable range (20-80 mM). Phosphatidylethanol production was activated only by phorbol derivatives that are activators of protein kinase C (i.e. TPA, 4 beta-phorbol-12,13-dibutyrate, and 4 beta-phorbol-12,13-didecanoate) and could be mimicked by a cell-permeant diacylglycerol, 1,2-dioctanoyl-sn-glycerol, in a nonadditive manner. The effect of TPA was inhibited by the protein kinase C inhibitor 1-(5-isoquinolinesulfonyl)-2-methylpiperazine (0.1 mM) by 70% but not by N-(2-guanidinoethyl)-5-isoquinolinesulfonamide. Phosphatidylethanol formation was completely abolished in cells in which protein kinase C was down-regulated by pretreatment of the cells with TPA. These results indicate that phosphatidylethanol biosynthesis in NG108-15 cells depends largely on activation of protein kinase C. In contrast to its effects on the release of free choline and on the accumulation of phosphatidylethanol, TPA did not affect the levels of phosphatidic acid in NG108-15 cells. It is therefore proposed that protein kinase C selectively activates the phosphatidyl transferase activity of phospholipase D, reflecting a signal termination mechanism which may be operative in phospholipase D-mediated signal transduction cascades.
12 - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)可刺激完整的NG108 - 15细胞将游离胆碱释放到培养基中,而不影响磷酸胆碱的释放(利斯科维奇,M.,布卢斯塔伊恩,J.K.,弗里斯,A.,和沃尔特曼,R.J.(1987年)《生物化学杂志》241卷,81 - 86页)。为了检验这一反应反映细胞磷脂酶D通过蛋白激酶C(钙/磷脂依赖性酶)被激活的假说,我在NG108 - 15细胞中检测了异常磷脂磷脂酰乙醇的生物合成,磷脂酰乙醇是由磷脂酶D在乙醇存在下通过转磷脂酰基作用产生的。通过测量磷脂酰部分(用[³H]油酸进行代谢预标记)掺入磷脂酰乙醇中的量来定量磷脂酰乙醇的产生。NG108 - 15细胞中磷脂酰乙醇的产生实际上依赖于TPA的刺激,呈时间和浓度依赖性(半数有效浓度=18 nM)。与TPA孵育10分钟后,³H - 磷脂酰乙醇的形成速率达到峰值,此后逐渐下降。TPA处理的细胞中³H - 磷脂酰乙醇的水平与生理可达到范围内的乙醇浓度直接相关(20 - 80 mM)。只有作为蛋白激酶C激活剂的佛波醇衍生物(即TPA、4β - 佛波醇 - 12,13 - 二丁酸酯和4β - 佛波醇 - 12,13 - 二癸酸酯)能激活磷脂酰乙醇的产生,并且可被细胞可渗透的二酰基甘油1,2 - 二辛酰 - sn - 甘油以非累加方式模拟。蛋白激酶C抑制剂1 - (5 - 异喹啉磺酰基) - 2 - 甲基哌嗪(0.1 mM)可使TPA的作用抑制70%,但N - (2 - 胍基乙基) - 5 - 异喹啉磺酰胺则无此作用。在用TPA预处理使蛋白激酶C下调的细胞中,磷脂酰乙醇的形成完全被消除。这些结果表明,NG108 - 15细胞中磷脂酰乙醇的生物合成在很大程度上依赖于蛋白激酶C的激活。与它对游离胆碱释放和磷脂酰乙醇积累的影响相反,TPA不影响NG108 - 15细胞中磷脂酸的水平。因此有人提出,蛋白激酶C选择性地激活磷脂酶D的磷脂转移酶活性,这反映了一种可能在磷脂酶D介导的信号转导级联反应中起作用的信号终止机制。