Kirk C J, Bone E A, Palmer S, Michell R H
J Recept Res. 1984;4(1-6):489-504. doi: 10.3109/10799898409042569.
The activation of Ca2+-mobilising receptors on hepatocytes and many other cells leads to a prompt reduction in the cellular content of inositol phospholipids. The primary event which underlies these changes is, most probably, a phospholipase C-catalysed attack upon phosphatidylinositol 4,5 bisphosphate. The receptor-mediated breakdown of this lipid in stimulated cells is: (i) not mediated by an increase in cytosol [Ca2+] and (ii) closely coupled to receptor occupation. Phosphatidylinositol 4,5 bisphosphate degradation may be studied by measuring the appearance of the water-soluble product, inositol trisphosphate (and its metabolites: inositol bisphosphate and inositol monophosphate), in stimulated cells. Recent evidence indicates that inositol trisphosphate and the lipid soluble product of phosphatidylinositol 4,5 bisphosphate breakdown, 1,2 diacylglycerol, may act as 'second messengers' which mediate the effects of many extracellular signals in stimulated cells.
肝细胞及许多其他细胞上钙动员受体的激活会导致肌醇磷脂的细胞含量迅速减少。这些变化背后的主要事件很可能是磷脂酶C催化对磷脂酰肌醇4,5 -二磷酸的攻击。在受刺激细胞中,这种脂质的受体介导分解:(i)不受胞质溶胶[Ca2+]增加的介导,(ii)与受体占据紧密偶联。磷脂酰肌醇4,5 -二磷酸的降解可通过测量受刺激细胞中水溶性产物肌醇三磷酸(及其代谢产物:肌醇二磷酸和肌醇一磷酸)的出现来研究。最近的证据表明,肌醇三磷酸和磷脂酰肌醇4,5 -二磷酸分解的脂溶性产物1,2 -二酰甘油可能作为“第二信使”,介导受刺激细胞中许多细胞外信号的作用。