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Development of a method to quantify platelet adhesion and aggregation under static conditions

机译:开发一种在静态条件下定量血小板粘附和聚集的方法

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摘要

Platelets are important players in hemostasis and thrombosis. Thus, accurate assessment of platelet function is crucial for identifying platelet function disorders and measuring the efficacy of antiplatelet therapies. We have developed a novel platelet aggregation technique that utilizes the physical parameter of platelet concentration in conjunction with volume and mass measurements to evaluate platelet adhesion and aggregation. Platelet aggregates were formed by incubating purified platelets on fibrinogen- or fibrillar collagen-coated surfaces at platelet concentrations ranging from 20,000 to 500,000 platelets/ L. Platelets formed aggregates under static conditions in a platelet concentration-dependent manner, with significantly greater mean volume and mass at higher platelet concentrations ( 400,000 platelets/ L). We show that a platelet glycoprotein IIb/IIIa inhibitor abrogated platelet-platelet aggregation, which significantly reduced the volume and mass of the platelets on the collagen surface. This static platelet aggregation technique is amenable to standardization and represents a useful tool to investigate the mechanism of platelet activation and aggregation under static conditions.
机译:血小板是止血和血栓形成的重要参与者。因此,准确评估血小板功能对于识别血小板功能障碍和测量抗血小板疗法的疗效至关重要。我们开发了一种新颖的血小板聚集技术,该技术利用血小板浓度的物理参数结合体积和质量测量来评估血小板粘附和聚集。血小板聚集物是通过在纤维蛋白原或原纤维胶原蛋白包被的表面上以20,000至500,000血小板/ L的血小板浓度孵育纯化的血小板而形成的。血小板在静态条件下以血小板浓度依赖的方式形成聚集体,平均体积和质量明显更高较高的血小板浓度(400,000血小板/ L)。我们表明,血小板糖蛋白IIb / IIIa抑制剂消除了血小板-血小板凝集,从而显着降低了胶原蛋白表面血小板的体积和质量。这种静态血小板聚集技术适合标准化,是研究静态条件下血小板活化和聚集机制的有用工具。

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