George J N, Lewis P C
J Lab Clin Med. 1978 Feb;91(2):301-6.
DD125ISA, which binds to platelet surface glycoproteins, is lost more rapidly from double-labeled circulating rabbit platelets than is 51Cr, a label of platelet cytoplasm. Treatment of rabbits with aspirin and dipyridamole to diminish platelet function did not affect 51Cr survival but inhibited DD125ISA loss so that it disappeared from the circulation at the same rate as 51Cr . Intravenous thrombin infusion increased DD125ISA loss relative to 51Cr loss. Therefore surface glycoprotein loss was prevented by agents which inhibit platelet function and was accelerated by intravascular coagulation. These observations support the hypothesis that platelet surface glycoprotein loss is a continuous process in the normal circulation which may occur during reversible contact interactions in the process of hemostasis and thrombosis.
DD125ISA可与血小板表面糖蛋白结合,相较于作为血小板细胞质标记物的51Cr,它从双标记循环兔血小板中消失得更快。用阿司匹林和双嘧达莫处理兔子以降低血小板功能,这并未影响51Cr的存活,但抑制了DD125ISA的丢失,使其从循环中消失的速率与51Cr相同。静脉输注凝血酶相对于51Cr的丢失增加了DD125ISA的丢失。因此,抑制血小板功能的药物可防止表面糖蛋白丢失,而血管内凝血则加速这种丢失。这些观察结果支持这样一种假说,即血小板表面糖蛋白丢失是正常循环中的一个持续过程,可能发生在止血和血栓形成过程中的可逆接触相互作用期间。