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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Effect of fibrinogen, fibrin, and fibrin degradation products on transendothelial migration of leukocytes
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Effect of fibrinogen, fibrin, and fibrin degradation products on transendothelial migration of leukocytes

机译:纤维蛋白原,纤维蛋白和纤维蛋白降解产物对白细胞颅骨迁移的影响

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摘要

In spite of numerous studies on the involvement of fibrinogen in transendothelial migration of leukocytes and thereby inflammation, there is still no clear understanding of which fibrin(ogen) species can stimulate leukocyte transmigration. Although we have previously proposed that interaction of fibrin with the VLDL receptor (VLDLR) promotes leukocyte transmigration, there is no direct experimental evidence for the involvement of fibrin in this process. To address these questions, we performed systematic studies of interaction of VLDLR with fibrinogen, fibrin, and their isolated recombinant B beta N- and beta N-domains, respectively, and the effect of various fibrin(ogen) species on transendothelial migration of leukocytes. The results obtained revealed that freshly purified fibrinogen does not interact with VLDLR in solution and has practically no effect on leukocyte transmigration. They also indicate that the VLDLR-binding site is cryptic in fibrinogen and becomes accessible upon its adsorption onto a surface or upon its conversion into fibrin. We also found that the D-D:E-1 complex and higher molecular mass fibrin degradation products, as well as soluble fibrin and fibrin polymers (clots) anchored to the endothelial monolayer, promote leukocyte transmigration mainly through the VLDL receptor-dependent pathway. Thus, the results of the present study suggest that fibrin degradation products and soluble fibrin that may be present in the circulation in vivo, as well as fibrin clots that may be deposited on the surface of inflamed endothelium, promote leukocyte transmigration. These findings further clarify the molecular mechanisms underlying the fibrin-VLDLR-dependent pathway of leukocyte transmigration and provide an explanation for a possible (patho) physiological role of this pathway.
机译:尽管有许多关于纤维蛋白原在白细胞颅脑迁移的纤维蛋白原的参与以及炎症的研究中,但仍然没有明确了解哪种纤维蛋白(ELING)物种可以刺激白细胞迁移。虽然我们先前已经提出了用VLDL受体(VLDLR)的纤维蛋白的相互作用促进白细胞迁移,但没有直接的实验证据参与纤维蛋白在该过程中。为了解决这些问题,我们对VLDLR与纤维蛋白原,纤维蛋白及其分离的重组BβN-和βN-结构域的相互作用进行了系统研究,以及各种纤维蛋白(ELIGON)物种对白细胞骨间迁移的影响。得到的结果表明,新鲜纯化的纤维蛋白原在溶液中没有与VLDLR相互作用,并且几乎没有对白细胞迁移的影响。它们还表明VLDLR结合位点在纤维蛋白原中是神秘的,并且在其吸附到表面上或转化为纤维蛋白时变得可进入。我们还发现D-D:E-1复合物和较高的分子量纤维蛋白降解产物,以及锚定到内皮单层的可溶性纤维蛋白和纤维蛋白聚合物(凝块),主要通过VLDL受体依赖性途径促进白细胞迁移。因此,本研究的结果表明,纤维蛋白降解产物和可溶性纤维蛋白可以存在于体内循环中,以及可沉积在发炎内皮表面的纤维蛋白凝聚,促进白细胞迁移。这些发现进一步阐明了白细胞迁移型纤维蛋白-VLDLR依赖性途径的分子机制,并对该途径的可能(PATO)生理作用提供了解释。

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