Lapetina E G, Watson S P
Nouv Rev Fr Hematol (1978). 1985;27(4):235-8.
Activation of platelets is correlated with phospholipase C-induced degradation of phosphatidylinositol 4,5-bisphosphate and the rapid formation of 1,2-diacylglycerol and myo-inositol 1,4,5-trisphosphate. Both products are considered second messengers and they, respectively, stimulate protein kinase C and Ca2+ mobilization. Mobilization of Ca2+ leads to activation of a Ca2+/calmodulin-dependent myosin light chain kinase and phospholipases A2 which liberate arachidonic acid from phospholipids. Arachidonate is then immediately converted to active endoperoxides and thromboxanes which are released and activate further platelets again through phospholipase C. The levels of phosphatidic acid and lysophosphatidic acid are also increased following receptor-stimulated hydrolysis of the inositol phospholipids. Lysophosphatidic acid might have a direct action on the opening of Ca2+-channels.
血小板的激活与磷脂酶C诱导的磷脂酰肌醇4,5-二磷酸降解以及1,2-二酰基甘油和肌醇1,4,5-三磷酸的快速形成相关。这两种产物均被视为第二信使,它们分别刺激蛋白激酶C和钙离子动员。钙离子动员导致钙/钙调蛋白依赖性肌球蛋白轻链激酶和磷脂酶A2激活,后者从磷脂中释放花生四烯酸。花生四烯酸随后立即转化为活性内过氧化物和血栓素,它们被释放并通过磷脂酶C再次激活更多血小板。在受体刺激的肌醇磷脂水解后,磷脂酸和溶血磷脂酸水平也会升高。溶血磷脂酸可能对钙离子通道的开放有直接作用。