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The secretion of von Willebrand factor from endothelial cells; an increasingly complicated story

机译:从血管内皮细胞分泌血管性假血友病因子;一个越来越复杂的故事

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摘要

von Willebrand factor (VWF) plays key roles in both primary and secondary hemostasis by capturing platelets and chaperoning clotting factor VIII, respectively. It is stored within the Weibel–Palade bodies (WPBs) of endothelial cells as a highly prothrombotic protein, and its release is thus necessarily under tight control. Regulating the secretion of VWF involves multiple layers of cellular machinery that act together at different stages, leading to the exocytic fusion of WPBs with the plasma membrane and the consequent release of VWF. This review aims to provide a snapshot of the current understanding of those components, in particular the members of the Rab family, acting in the increasingly complex story of VWF secretion.
机译:血管性血友病因子(VWF)通过分别捕获血小板和伴侣凝血因子VIII在原发性和继发性止血中起关键作用。它以高血栓前蛋白的形式存储在内皮细胞的Weibel-Palade体(WPB)中,因此其释放必须受到严格控制。调节VWF的分泌涉及在不同阶段共同起作用的多层细胞机器,从而导致WPB与质膜的胞外融合,并最终释放VWF。这篇综述旨在提供对这些成分,特别是Rab家族成员,在越来越复杂的VWF分泌故事中起作用的最新了解。

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