Mourik Marjon, Eikenboom Jeroen
Jeroen Eikenboom, Leiden University Medical Center, Department of Thrombosis and Haemostasis, C7-61, P.O. Box 9600, 2300 RC Leiden, The Netherlands, Tel: +31 71 526 4906, E-Mail:
Hamostaseologie. 2017 Jan 31;37(1):13-24. doi: 10.5482/HAMO-16-07-0021. Epub 2016 Dec 22.
Weibel-Palade bodies (WPBs) are rod or cigar-shaped secretory organelles that are formed by the vascular endothelium. They contain a diverse set of proteins that either function in haemostasis, inflammation, or angiogenesis. Biogenesis of the WPB occurs at the Golgi apparatus in a process that is dependent on the main component of the WPB, the haemostatic protein von Willebrand Factor (VWF). During this process the organelle is directed towards the regulated secretion pathway by recruiting the machinery that responds to exocytosis stimulating agonists. Upon maturation in the periphery of the cell the WPB recruits Rab27A which regulates WPB secretion. To date several signaling pathways have been found to stimulate WPB release. These signaling pathways can trigger several secretion modes including single WPB release and multigranular exocytosis. In this review we will give an overview of the WPB lifecycle from biogenesis to secretion and we will discuss several deficiencies that affect the WPB lifecycle.
魏贝尔-帕拉德小体(WPBs)是由血管内皮细胞形成的杆状或雪茄状分泌细胞器。它们包含多种蛋白质,这些蛋白质在止血、炎症或血管生成中发挥作用。WPB的生物发生在高尔基体中进行,该过程依赖于WPB的主要成分——止血蛋白血管性血友病因子(VWF)。在此过程中,细胞器通过招募响应胞吐刺激激动剂的机制被导向调节性分泌途径。在细胞外周成熟后,WPB招募Rab27A,其调节WPB的分泌。迄今为止,已发现几种信号通路可刺激WPB释放。这些信号通路可触发多种分泌模式,包括单个WPB释放和多颗粒胞吐。在本综述中,我们将概述WPB从生物发生到分泌的生命周期,并讨论影响WPB生命周期的几种缺陷。