Mouillac B, Balestre M N, Guillon G
Centre CNRS-INSERM de Pharmacologie-Endocrinologie, Montpellier, France.
Biochem Biophys Res Commun. 1989 Mar 31;159(3):953-60. doi: 10.1016/0006-291x(89)92201-8.
In the rat mammary tumoral cell line (WRK1 cells), vasopressin was previously described to stimulate a phospholipase C. In this study, we have analysed the effect of vasopressin both on intracellular calcium mobilization and on the accumulation of inositol phosphates. Maximal concentration of vasopressin simultaneously induces an accumulation of Ins(1,4,5)P3 and a rise of intracellular calcium concentration. Both these two phenomena are transient and exhibit similar kinetics. A sustained accumulation of InsP2, Ins(1,3,4)P3 and InsP are observed later. Yet no stimulation of InsP4 can be objectified. These results indicate that Ins(1,4,5)P3 is the major inositol phosphate involved in intracellular calcium mobilization.
在大鼠乳腺肿瘤细胞系(WRK1细胞)中,先前已描述血管加压素可刺激磷脂酶C。在本研究中,我们分析了血管加压素对细胞内钙动员和肌醇磷酸积累的影响。血管加压素的最大浓度同时诱导Ins(1,4,5)P3的积累和细胞内钙浓度的升高。这两种现象都是短暂的,并且表现出相似的动力学。随后观察到InsP2、Ins(1,3,4)P3和InsP的持续积累。然而,未观察到对InsP4的刺激作用。这些结果表明,Ins(1,4,5)P3是参与细胞内钙动员的主要肌醇磷酸。