Price B D, Morris J D, Hall A
Institute of Cancer Research, Chester Beatty Laboratories, London, U.K.
Biochem J. 1989 Dec 1;264(2):509-15. doi: 10.1042/bj2640509.
The effect of a number of growth factors on phosphatidylcholine (PtdCho) turnover in Swiss-3T3 cells was studied. Phorbol 12-myristate 13-acetate (PMA), bombesin, platelet-derived growth factor (PDGF) and vasopressin rapidly stimulated PtdCho hydrolysis, diacylglycerol (DAG) production, and PtdCho synthesis. Insulin and prostaglandin F2 alpha (PGF2 alpha) stimulated PtdCho synthesis, but not its breakdown, whereas epidermal growth factor (EGF) and bradykinin were without effect. Stimulation of PtdCho hydrolysis by the above ligands resulted in increased production of phosphocholine and DAG (due to phospholipase C activity) and significant amounts of choline, suggesting activation of a phospholipase D as well. CDP-choline and glycerophosphocholine levels were unchanged. Down-regulation of protein kinase C with PMA (400 nM, 40 h) abolished the stimulation of PtdCho hydrolysis and PtdCho synthesis by PMA, bombesin, PDGF and vasopressin, but not the stimulation of PtdCho synthesis by insulin and PGF2 alpha. PtdCho hydrolysis therefore occurs predominantly by activation of protein kinase C (either by PMA or PtdIns hydrolysis) leading to elevation of DAG levels derived from non-PtdIns(4,5)P2 sources. PtdCho synthesis occurs by both a protein kinase C-dependent pathway (stimulated by PMA, PDGF, bombesin and vasopressin) and a protein kinase C-independent pathway (stimulated by insulin and PGF2 alpha). DAG production from PtdCho hydrolysis is not the primary signal to activate protein kinase C, but may contribute to long-term activation of this kinase.
研究了多种生长因子对瑞士3T3细胞中磷脂酰胆碱(PtdCho)周转的影响。佛波酯12-肉豆蔻酸酯13-乙酸酯(PMA)、蛙皮素、血小板衍生生长因子(PDGF)和血管加压素迅速刺激PtdCho水解、二酰基甘油(DAG)生成以及PtdCho合成。胰岛素和前列腺素F2α(PGF2α)刺激PtdCho合成,但不刺激其分解,而表皮生长因子(EGF)和缓激肽则无作用。上述配体对PtdCho水解的刺激导致磷酸胆碱和DAG产量增加(由于磷脂酶C活性)以及大量胆碱生成,这表明磷脂酶D也被激活。CDP-胆碱和甘油磷酸胆碱水平未发生变化。用PMA(400 nM,40小时)下调蛋白激酶C可消除PMA、蛙皮素、PDGF和血管加压素对PtdCho水解和PtdCho合成的刺激,但不能消除胰岛素和PGF2α对PtdCho合成的刺激。因此,PtdCho水解主要通过激活蛋白激酶C(通过PMA或磷脂酰肌醇水解)发生,导致源自非磷脂酰肌醇(4,5)二磷酸(PtdIns(4,5)P2)来源的DAG水平升高。PtdCho合成通过蛋白激酶C依赖性途径(由PMA、PDGF、蛙皮素和血管加压素刺激)和蛋白激酶C非依赖性途径(由胰岛素和PGF2α刺激)发生。PtdCho水解产生的DAG不是激活蛋白激酶C的主要信号,但可能有助于该激酶的长期激活。