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首页> 外文期刊>Arteriosclerosis, thrombosis, and vascular biology >Orchestration of Primary Hemostasis by Platelet and Endothelial Lysosome-Related Organelles
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Orchestration of Primary Hemostasis by Platelet and Endothelial Lysosome-Related Organelles

机译:血小板和内皮溶酶体相关细胞器的原发性止血的康体

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Megakaryocyte-derived platelets and endothelial cells store their hemostatic cargo in α- and δ-granules and Weibel-Palade bodies, respectively. These storage granules belong to the lysosome-related organelles (LROs), a heterogeneous group of organelles that are rapidly released following agonist-induced triggering of intracellular signaling pathways. Following vascular injury, endothelial Weibel-Palade bodies release their content into the vascular lumen and promote the formation of long VWF (von Willebrand factor) strings that form an adhesive platform for platelets. Binding to VWF strings as well as exposed subendothelial collagen activates platelets resulting in the release of α- and δ-granules, which are crucial events in formation of a primary hemostatic plug. Biogenesis and secretion of these LROs are pivotal for the maintenance of proper hemostasis. Several bleeding disorders have been linked to abnormal generation of LROs in megakaryocytes and endothelial cells. Recent reviews have emphasized common pathways in the biogenesis and biological properties of LROs, focusing mainly on melanosomes. Despite many similarities, LROs in platelet and endothelial cells clearly possess distinct properties that allow them to provide a highly coordinated and synergistic contribution to primary hemostasis by sequentially releasing hemostatic cargo. In this brief review, we discuss in depth the known regulators of α- and δ-granules in megakaryocytes/platelets and Weibel-Palade bodies in endothelial cells, starting from transcription factors that have been associated with granule formation to protein complexes that promote granule maturation. In addition, we provide a detailed view on the interplay between platelet and endothelial LROs in controlling hemostasis as well as their dysfunction in LRO related bleeding disorders.
机译:巨核细胞衍生的血小板和内皮细胞分别在α-和δ-颗粒和Weibel-Palade体中储存它们的止血货物。这些储存颗粒属于溶酶体相关的细胞器(LROS),一种不均匀的细胞器组,其迅速释放在诱导的细胞内信号传导途径的触发后迅速释放。在血管损伤后,内皮尾焊体均可将其含量释放到血管内腔中,并促进形成长VWF(Von Willebrand因子)字符串,形成血小板的粘合剂平台。与VWF串以及暴露的下属胶原蛋白结合,激活血小板,导致α-和δ-颗粒的释放,这是形成初级止血塞的关键事件。这些LRO的生物发生和分泌是为了维持适当的止血的枢转。几种出血障碍已与巨核细胞和内皮细胞的异常产生相连。最近的评价强调了LRO生物发生和生物学性质的常见途径,主要关注黑色素。尽管存在许多相似之处,但血小板和内皮细胞中的LRO清楚地具有明显的性质,使它们通过顺序释放止血货物来为初级止血提供高度协调和协同贡献。在这篇简短的综述中,我们在深度中讨论了甲状腺细胞/血小板和内皮细胞中的α-和δ-颗粒的已知调节因子,从促进颗粒成熟的蛋白质复合物相关的转录因子开始。此外,我们提供了对控制止血和内皮LRO之间的相互作用的详细视图,以及它们在联系相关出血障碍中的功能障碍。

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