MRC Laboratory of Molecular Cell Biology, University College London, Gower Street, London, WC1E6BT, UK.
MRC Laboratory of Molecular Cell Biology, University College London, Gower Street, London, WC1E6BT, UK
J Cell Sci. 2017 Nov 1;130(21):3611-3617. doi: 10.1242/jcs.208033.
The vascular environment can rapidly alter, and the speed with which responses to both physiological and pathological changes are required necessitates the existence of a highly responsive system. The endothelium can quickly deliver bioactive molecules by regulated exocytosis of its secretory granules, the Weibel-Palade bodies (WPBs). WPBs include proteins that initiate both haemostasis and inflammation, as well those that modulate blood pressure and angiogenesis. WPB formation is driven by von Willebrand factor, their most abundant protein, which controls both shape and size of WPBs. WPB are generated in a range of sizes, with the largest granules over ten times the size of the smallest. In this Cell Science at a Glance and the accompanying poster, we discuss the emerging mechanisms by which WPB size is controlled and how this affects the ability of this organelle to modulate haemostasis. We will also outline the different modes of exocytosis and their polarity that are currently being explored, and illustrate that these large secretory organelles provide a model for how elements of secretory granule biogenesis and exocytosis cooperate to support a complex and diverse set of functions.
血管环境可以迅速改变,而对生理和病理变化的反应速度则需要一个高度敏感的系统。内皮细胞可以通过其分泌颗粒(Weibel-Palade 小体,WPB)的受调控的胞吐作用快速地输送生物活性分子。WPB 包含启动止血和炎症的蛋白质,以及调节血压和血管生成的蛋白质。WPB 的形成由其最丰富的蛋白质 von Willebrand 因子驱动,该因子控制 WPB 的形状和大小。WPB 可以形成多种大小,最大的颗粒比最小的颗粒大十倍以上。在这篇《细胞科学亮点》和配套海报中,我们讨论了 WPB 大小控制的新机制,以及这如何影响该细胞器调节止血的能力。我们还将概述目前正在探索的不同胞吐作用模式及其极性,并说明这些大型分泌细胞器为分泌颗粒生物发生和胞吐作用的元素如何合作以支持一组复杂多样的功能提供了模型。