Putney J W, Takemura H, Hughes A R, Horstman D A, Thastrup O
Laboratory of Cellular and Molecular Pharmacology, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709.
FASEB J. 1989 Jun;3(8):1899-905. doi: 10.1096/fasebj.3.8.2542110.
Activation of a variety of cell surface receptors results in the phospholipase C-catalyzed hydrolysis of the minor plasma membrane phospholipid phosphatidylinositol 4,5-bisphosphate, with concomitant formation of inositol 1,4,5-trisphosphate and diacylglycerol. There is strong evidence that inositol 1,4,5-trisphosphate stimulates Ca2+ release from intracellular stores. The Ca2+-releasing actions of inositol 1,4,5-trisphosphate are terminated by its metabolism through two distinct pathways. Inositol 1,4,5-trisphosphate is dephosphorylated by a 5-phosphatase to inositol 1,4-bisphosphate; alternatively, inositol 1,4,5-trisphosphate can also be phosphorylated to inositol 1,3,4,5-tetrakisphosphate by a 3-kinase. Although the mechanism of Ca2+ mobilization is understood, the precise mechanisms involved in Ca2+ entry are not known; the proposal that inositol 1,4,5-trisphosphate secondarily elicits Ca2+ entry by emptying an intracellular Ca2+ pool is considered.
多种细胞表面受体的激活会导致磷脂酶C催化水解少量质膜磷脂磷脂酰肌醇4,5 - 二磷酸,同时形成肌醇1,4,5 - 三磷酸和二酰基甘油。有充分证据表明,肌醇1,4,5 - 三磷酸会刺激细胞内储存库释放Ca2+。肌醇1,4,5 - 三磷酸的Ca2+释放作用通过两条不同途径的代谢而终止。肌醇1,4,5 - 三磷酸被5 - 磷酸酶去磷酸化为肌醇1,4 - 二磷酸;另外,肌醇1,4,5 - 三磷酸也可被3 - 激酶磷酸化为肌醇1,3,4,5 - 四磷酸。虽然Ca2+动员的机制已为人所知,但Ca2+进入所涉及的精确机制尚不清楚;有人认为肌醇1,4,5 - 三磷酸通过排空细胞内Ca2+池而继发引起Ca2+进入。