Kometani M, Sato T, Fujii T
Thromb Res. 1986 Mar 15;41(6):801-9. doi: 10.1016/0049-3848(86)90378-6.
We investigated the role of cytoskeletal components in platelet activation under conditions in which changes in the shape of platelets, their secreting reaction, or both, would occur. When rabbit platelets were stimulated with 0.1 U/ml thrombin, they changed their shape, secreted serotonin, and incorporated actin-binding protein (ABP), myosin, and actin into their cytoskeletons. Platelets treated with 2 microM cytochalasin E and stimulated with 0.1 U/ml thrombin secreted serotonin and assembled myosin and actin into their cytoskeletons, but did not change in shape. Stimulation with a low dose of thrombin (0.001 U/ml) or ADP (10 microM) caused a change in shape and incorporation of ABP, myosin, and actin, but not serotonin secretion. These results suggest that the assembly of myosin and actin into platelet cytoskeletons is related to the secreting reaction, and that ABP, myosin, and actin are all involved in the changes in platelet shape.
我们研究了细胞骨架成分在血小板活化过程中的作用,在此过程中血小板的形状会发生变化,其分泌反应也会发生变化,或者两者兼而有之。当用0.1 U/ml凝血酶刺激兔血小板时,它们会改变形状、分泌5-羟色胺,并将肌动蛋白结合蛋白(ABP)、肌球蛋白和肌动蛋白整合到其细胞骨架中。用2 microM细胞松弛素E处理的血小板,再用0.1 U/ml凝血酶刺激,会分泌5-羟色胺,并将肌球蛋白和肌动蛋白组装到其细胞骨架中,但形状没有改变。用低剂量凝血酶(0.001 U/ml)或ADP(10 microM)刺激会导致形状改变以及ABP、肌球蛋白和肌动蛋白的整合,但不会引起5-羟色胺分泌。这些结果表明,肌球蛋白和肌动蛋白组装到血小板细胞骨架中与分泌反应有关,并且ABP、肌球蛋白和肌动蛋白均参与血小板形状的变化。