Bevers E M, Comfurius P, Zwaal R F
Biochim Biophys Acta. 1983 Dec 7;736(1):57-66. doi: 10.1016/0005-2736(83)90169-4.
Exposure of phospholipids at the outer surface of activated and control platelets was studied by incubation with a mixture of phospholipase A2 from Naja naja and bee venom, solely or in combination with sphingomyelinase from Staphylococcus aureus, using conditions under which cell lysis remained below 10%. Incubation with phospholipase A2 alone revealed a markedly increased susceptibility of the phospholipids in platelets activated by a mixture of collagen plus thrombin, by the SH-oxidizing compound diamide, or by calcium ionophore A23187, as compared to control platelets or platelets activated separately by collagen or thrombin. Collagen plus thrombin, diamide, and ionophore treated platelets revealed an increased exposure of phosphatidylserine at the outer surface accompanied by a decreased exposure of sphingomyelin, as could be concluded from incubations with a combination of phospholipase A2 and sphingomyelinase. These alterations were much less apparent in platelets activated either by thrombin or by collagen alone. The increased exposure of phosphatidylserine in activated platelets is accompanied by an increased ability of the platelets to enhance the conversion of prothrombin to thrombin by coagulation factor Xa, in the presence of factor Va and calcium. It is concluded that the altered orientation of the phospholipids in the plasma membrane of platelets activated by collagen plus thrombin, by diamide, or by calcium ionophore, is the result of a transbilayer movement. Moreover, the increased exposure of phosphatidylserine in platelets stimulated by the combined action of collagen and thrombin might be of considerable importance for the hemostatic process.
通过将来自眼镜蛇和蜂毒的磷脂酶A2单独或与来自金黄色葡萄球菌的鞘磷脂酶联合孵育,在细胞裂解率保持在10%以下的条件下,研究了活化血小板和对照血小板外表面磷脂的暴露情况。与对照血小板或单独由胶原蛋白或凝血酶激活的血小板相比,单独用磷脂酶A2孵育显示,由胶原蛋白加凝血酶混合物、SH氧化化合物二酰胺或钙离子载体A23187激活的血小板中的磷脂敏感性显著增加。从用磷脂酶A2和鞘磷脂酶联合孵育可以得出结论,胶原蛋白加凝血酶、二酰胺和离子载体处理的血小板外表面磷脂酰丝氨酸暴露增加,同时鞘磷脂暴露减少。这些改变在单独由凝血酶或胶原蛋白激活的血小板中不太明显。在因子Va和钙存在的情况下,活化血小板中磷脂酰丝氨酸暴露增加伴随着血小板增强凝血因子Xa将凝血酶原转化为凝血酶的能力增强。得出结论,由胶原蛋白加凝血酶、二酰胺或钙离子载体激活的血小板质膜中磷脂方向的改变是跨膜运动的结果。此外,胶原蛋白和凝血酶联合作用刺激的血小板中磷脂酰丝氨酸暴露增加可能对止血过程具有相当重要的意义。