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Platelet morphologic changes and fibrinogen receptor localization. Initial responses in ADP-activated human platelets.

机译:血小板形态变化和纤维蛋白原受体定位。 ADP激活的人类血小板的初始反应。

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摘要

Platelet exposure to agonists results in rapid morphologic changes paralleled by fibrinogen binding and platelet aggregation. The current study used standardized stereology in conjunction with immunogold electron microscopy to correlate the initial morphologic changes with fibrinogen receptor localization on the surfaces of ADP-activated human platelets. A 45% increase in platelet circumference was observed after 3 seconds of activation (P = 0.001). Virtually all of this increase was due to a 13-fold increase in projection membrane, and the projections observed by stereo microscopy at this time were mostly blunt. Both blunt and long projections also accounted for the increase in platelet-platelet contacts at 10 seconds of activation. Immunogold electron microscopy using the monoclonal antibodies P2 and AP-2 against the fibrinogen receptor, glycoprotein IIb/IIIa (GP IIb/IIIa), showed relatively equivalent immunogold densities on projections compared with cell body during 30 seconds of activation. The activation-dependent anti-GP IIb/IIIa monoclonal antibody, 7E3, showed an immunogold density 37% greater on projections compared with cell body (P = 0.0001). Colocalization studies using 7E3 with a polyclonal antifibrinogen antibody showed bound fibrinogen in close proximity to the GP IIb/IIIa localized by 7E3 on projections. These studies support an important role for platelet projections during the earliest stages of fibrinogen binding and ADP-induced aggregation.
机译:血小板暴露于激动剂会导致快速的形态变化,并伴有纤维蛋白原结合和血小板聚集。目前的研究使用标准化的立体学技术结合免疫金电子显微镜技术,将初始形态学变化与纤维蛋白原受体在ADP激活的人类血小板表面的定位相关联。激活3秒后观察到血小板周长增加了45%(P = 0.001)。实际上,所有这些增加都是由于投射膜增加了13倍,此时通过体视显微镜观察到的投射大多是钝的。钝的和长的突起也都说明了激活10秒后血小板与血小板接触的增加。使用抗纤维蛋白原受体糖蛋白IIb / IIIa(GP IIb / IIIa)的单克隆抗体P2和AP-2进行的免疫金电子显微镜观察,在激活30秒内,与细胞体相比,投影上的免疫金密度相对相等。与细胞体相比,激活依赖性抗GP IIb / IIIa单克隆抗体7E3的免疫金密度在投影上显示高37%(P = 0.0001)。使用7E3与多克隆抗纤维蛋白原抗体的共定位研究表明,结合的纤维蛋白原与投影上7E3所定位的GP IIb / IIIa非常接近。这些研究支持在纤维蛋白原结合和ADP诱导的聚集的最早阶段对血小板投射具有重要作用。

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