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血小板分离与活化检测

Platelet Isolation and Activation Assays.

作者信息

Burzynski Laura C, Pugh Nicholas, Clarke Murray C H

机构信息

Division of Cardiovascular Medicine, Department of Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.

School of Life Sciences, Anglia Ruskin University, Cambridge, UK.

出版信息

Bio Protoc. 2019 Oct 20;9(20):e3405. doi: 10.21769/BioProtoc.3405.

Abstract

Platelets regulate hemostasis and are the key determinants of pathogenic thrombosis following atherosclerotic plaque rupture. Platelets circulate in an inactive state, but become activated in response to damage to the endothelium, which exposes thrombogenic material such as collagen to the blood flow. Activation results in a number of responses, including secretion of soluble bioactive molecules via the release of alpha and dense granules, activation of membrane adhesion receptors, release of microparticles, and externalization of phosphatidylserine. These processes facilitate firm adhesion to sites of injury and the recruitment and activation of other platelets and leukocytes, resulting in aggregation and thrombus formation. Platelet activation drives the hemostatic response, and also contributes to pathogenic thrombus formation. Thus, quantification of platelet-associated responses is key to many pathophysiologically relevant processes. Here we describe protocols for isolating, counting, and activating platelets, and for the rapid quantification of cell surface proteins using flow cytometry.

摘要

血小板调节止血,并且是动脉粥样硬化斑块破裂后致病性血栓形成的关键决定因素。血小板以非活性状态循环,但会因内皮损伤而被激活,内皮损伤会使诸如胶原蛋白等促血栓形成物质暴露于血流中。激活会引发一系列反应,包括通过α颗粒和致密颗粒的释放来分泌可溶性生物活性分子、膜黏附受体的激活、微粒的释放以及磷脂酰丝氨酸的外化。这些过程有助于牢固黏附于损伤部位,并募集和激活其他血小板及白细胞,从而导致聚集和血栓形成。血小板激活驱动止血反应,也促成致病性血栓形成。因此,对血小板相关反应进行量化是许多病理生理相关过程的关键。在此,我们描述了分离、计数和激活血小板,以及使用流式细胞术快速量化细胞表面蛋白的方案。

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