首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Deposition of fibrinogen on the surface of in vitro thrombi prevents platelet adhesion
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Deposition of fibrinogen on the surface of in vitro thrombi prevents platelet adhesion

机译:纤维蛋白原沉积在体外血栓表面可防止血小板粘附

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摘要

The initial accumulation of platelets after vessel injury is followed by thrombin-mediated generation of fibrin which is deposited around the plug. While numerous in vitro studies have shown that fibrin is highly adhesive for platelets, the surface of experimental thrombi in vivo contains very few platelets suggesting the existence of natural anti-adhesive mechanisms protecting stabilized thrombi from platelet accumulation and continuous thrombus propagation. We previously showed that adsorption of fibrinogen on pure fibrin clots results in the formation of a nonadhesive matrix, highlighting a possible role of this process in surface-mediated control of thrombus growth. However, the deposition of fibrinogen on the surface of blood clots has not been examined. In this study, we investigated the presence of intact fibrinogen on the surface of fibrin-rich thrombi generated from flowing blood and determined whether deposited fibrinogen is nonadhesive for platelets. Stabilized fibrin-rich thrombi were generated using a flow chamber and the time that platelets spend on the surface of thrombi was determined by video recording. The presence of fibrinogen and fibrin on the surface of thrombi was analyzed by confocal microscopy using specific antibodies. Examination of the spatial distribution of two proteins revealed the presence of intact fibrinogen on the surface of stabilized thrombi. By manipulating the surface of thrombi to display either fibrin or intact fibrinogen, we found that platelets adhere to fibrin-but not to fibrinogen-coated thrombi. These results indicate that the fibrinogen matrix assembled on the outer layer of stabilized in vitro thrombi protects them from platelet adhesion. (C) 2015 Elsevier Ltd. All rights reserved.
机译:血管损伤后血小板的最初积累,随后是凝血酶介导的纤维蛋白生成,其沉积在栓塞周围。尽管大量的体外研究表明血纤蛋白对血小板具有很高的粘附性,但体内实验性血栓的表面却含有很少的血小板,这表明存在天然的抗粘附机制,可保护稳定的血栓免受血小板的积累和血栓的持续传播。我们以前表明,血纤蛋白原在纯血纤蛋白凝块上的吸附会导致形成非粘性基质,从而突出了该过程在血栓生长的表面介导控制中的可能作用。然而,尚未检查纤维蛋白原在血块表面上的沉积。在这项研究中,我们调查了从流动的血液中产生的富含纤维蛋白的血栓表面上完整纤维蛋白原的存在,并确定沉积的纤维蛋白原是否对血小板无粘附力。使用流动室产生稳定的富含纤维蛋白的血栓,并通过视频记录确定血小板在血栓表面的停留时间。使用特异性抗体通过共聚焦显微镜分析血栓表面纤维蛋白原和纤维蛋白的存在。检查两种蛋白质的空间分布表明稳定的血栓表面存在完整的纤维蛋白原。通过操纵血栓的表面以显示血纤蛋白或完整的血纤蛋白原,我们发现血小板粘附在血纤蛋白上,而不粘附在血纤蛋白原包被的血栓上。这些结果表明,组装在稳定的体外血栓外层上的纤维蛋白原基质可保护其免受血小板粘附。 (C)2015 Elsevier Ltd.保留所有权利。

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