Hannah Matthew J, Williams Ross, Kaur Jasber, Hewlett Lindsay J, Cutler Daniel F
MRC Laboratory for Molecular Cell Biology, Cell Biology Unit, University College London, Gower Street, WC1E 6BT, London, UK.
Semin Cell Dev Biol. 2002 Aug;13(4):313-24. doi: 10.1016/s1084-9521(02)00061-7.
Weibel-Palade bodies (WPBs) are the lysosome-related secretory organelles of endothelial cells. Their content protein von Willebrand factor, plays a key role in haemostasis, whilst P-selectin in the membranes is critical in the initiation of inflammation. Biogenesis of these rod-shaped structures is driven by von Willebrand factor, since its heterologous expression leads to formation of organelles morphologically indistinguishable from bona fide WPBs. The two main membrane proteins of WPBs, CD63 and P-selectin, have complex itineraries controlled largely by cytoplasmic targeting signals. We are only just beginning to understand the way in which these three proteins come together to form mature WPBs.
魏贝尔-帕拉德小体(WPBs)是内皮细胞中与溶酶体相关的分泌细胞器。其所含蛋白质血管性血友病因子在止血过程中起关键作用,而膜上的P-选择素在炎症起始中至关重要。这些杆状结构的生物发生由血管性血友病因子驱动,因为其异源表达会导致形成在形态上与真正的WPBs无法区分的细胞器。WPBs的两种主要膜蛋白CD63和P-选择素具有复杂的行程,主要由细胞质靶向信号控制。我们才刚刚开始了解这三种蛋白质如何聚集在一起形成成熟的WPBs。