[The role of adhesive proteins and membrane interactions in the processes of thrombocyte aggregation].

N V Belitser, M G Anishchuk, T M Pozdniakova, O V Gorkun, V I Veklich, T R Smekhova
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Abstract

The reported data concerning the role of fibrinogen in platelet aggregation are reviewed and compared to the authors' experimental data obtained by electron microscopy and cytochemical techniques. Using fibrinogen and fibrinogen antibodies bound to colloidal gold, it has been shown that the presence of fibrinogen bridged between the adjoining cells is not necessary for primary platelet microaggregation stimulated by ADP or thrombin. The formation of direct interplatelet contacts resembling "pentalaminar membranes" has been shown to participate in that process. Some mechanisms are proposed to explain the enhanced adhesiveness of the activated platelet surfaces. Redistribution of phospholipids in the membrane bilayer leading to the exposure of negatively charged phospholipids may underlie that phenomenon. The clustering and internalization of "occupied" membrane receptors may also contribute to the formation of close contacts between platelets stimulated by primary agonists in the presence of exogenous fibrinogen and other adhesive proteins.

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[粘附蛋白和膜相互作用在血小板聚集过程中的作用]。
本文回顾了纤维蛋白原在血小板聚集中的作用,并与作者通过电镜和细胞化学技术获得的实验数据进行了比较。利用与胶体金结合的纤维蛋白原和纤维蛋白原抗体,已经证明相邻细胞之间桥接的纤维蛋白原的存在对于ADP或凝血酶刺激的原发性血小板微聚集不是必需的。类似于“五层膜”的血小板间直接接触的形成已被证明参与了这一过程。提出了一些机制来解释活化血小板表面的粘附性增强。磷脂在膜双分子层中的重新分配导致带负电荷的磷脂暴露可能是这种现象的基础。在外源性纤维蛋白原和其他粘附蛋白存在的情况下,“占位”膜受体的聚集和内化也可能有助于在初级激动剂刺激下血小板之间形成密切接触。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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