Welsh C J, Cao H T, Chabbott H, Cabot M C
Lipid Biochemistry Laboratory, W. Alton Jones Cell Science Center, Inc., Lake Placid, NY 12946.
Biochem Biophys Res Commun. 1988 Apr 29;152(2):565-72. doi: 10.1016/s0006-291x(88)80075-5.
Vasopressin stimulates phosphatidylcholine hydrolysis in REF52 cells, and this phosphatidylcholine hydrolysis results in increases in choline containing metabolites in the culture medium (2.3 x control levels) and accumulation of cellular diacylglycerol (6.5 x control levels). Vasopressin is the only component of a 6-component mixture of the serum-free medium for REF52 cells that induces the phosphatidylcholine hydrolysis response. The effect of vasopressin is both time- and concentration-dependent. Maximal levels of both phosphatidyl-choline hydrolysis and accumulation of diacylglycerol are observed between 10 and 20 min after treatment with vasopressin. Effects are maximal at vasopressin concentrations of 100 ng/ml; the ED50 for vasopressin-stimulated phosphatidyl-choline hydrolysis is approximately 0.7 ng/ml. The evolution of diacylglycerol occurs in a time frame that is consistent with the diacylglycerol activating protein kinase C in a "second phase" agonist response.
血管加压素刺激REF52细胞中的磷脂酰胆碱水解,这种磷脂酰胆碱水解导致培养基中含胆碱代谢物增加(为对照水平的2.3倍)以及细胞二酰基甘油积累(为对照水平的6.5倍)。血管加压素是REF52细胞无血清培养基的六组分混合物中唯一能诱导磷脂酰胆碱水解反应的成分。血管加压素的作用具有时间和浓度依赖性。在用血管加压素处理后10至20分钟之间观察到磷脂酰胆碱水解和二酰基甘油积累的最高水平。在血管加压素浓度为100 ng/ml时作用最大;血管加压素刺激磷脂酰胆碱水解的半数有效剂量约为0.7 ng/ml。二酰基甘油的生成发生在一个与二酰基甘油在“第二阶段”激动剂反应中激活蛋白激酶C一致的时间范围内。