Molecular and Clinical Sciences Research Institute, St George's, University of London, London SW18 ORE, UK.
MRC National Institute for Medical Research, London NW7 1AA, UK.
J Cell Sci. 2019 Feb 15;132(5):jcs221952. doi: 10.1242/jcs.221952.
Elevations of intracellular free Ca concentration ([Ca]) are a potent trigger for Weibel-Palade body (WPB) exocytosis and secretion of von Willebrand factor (VWF) from endothelial cells; however, the identity of WPB-associated Ca-sensors involved in transducing acute increases in [Ca] into granule exocytosis remains unknown. Here, we show that synaptotagmin 5 (SYT5) is expressed in human umbilical vein endothelial cells (HUVECs) and is recruited to WPBs to regulate Ca-driven WPB exocytosis. Western blot analysis of HUVECs identified SYT5 protein, and exogenously expressed SYT5-mEGFP localised almost exclusively to WPBs. shRNA-mediated knockdown of endogenous SYT5 (shSYT5) reduced the rate and extent of histamine-evoked WPB exocytosis and reduced secretion of the WPB cargo VWF-propeptide (VWFpp). The shSYT5-mediated reduction in histamine-evoked WPB exocytosis was prevented by expression of shRNA-resistant SYT5-mCherry. Overexpression of SYT5-EGFP increased the rate and extent of histamine-evoked WPB exocytosis, and increased secretion of VWFpp. Expression of a Ca-binding defective SYT5 mutant (SYT5-Asp197Ser-EGFP) mimicked depletion of endogenous SYT5. We identify SYT5 as a WPB-associated Ca sensor regulating Ca-dependent secretion of stored mediators from vascular endothelial cells.
细胞内游离钙浓度 ([Ca]) 的升高是威伯尔-帕拉德体 (WPB) 胞吐和血管内皮细胞中 von Willebrand 因子 (VWF) 分泌的有效触发因素;然而,参与将 [Ca] 的急性增加转化为颗粒胞吐的 WPB 相关钙传感器的身份尚不清楚。在这里,我们表明突触结合蛋白 5 (SYT5) 在人脐静脉内皮细胞 (HUVEC) 中表达,并被募集到 WPB 以调节 Ca 驱动的 WPB 胞吐作用。HUVEC 的 Western blot 分析鉴定了 SYT5 蛋白,并且外源性表达的 SYT5-mEGFP 几乎仅定位于 WPB。内源性 SYT5 (shSYT5) 的 shRNA 介导敲低降低了组胺诱导的 WPB 胞吐作用的速率和程度,并降低了 WPB 货物 VWF 前肽 (VWFpp) 的分泌。表达 shRNA 抗性 SYT5-mCherry 可防止 shSYT5 介导的组胺诱导的 WPB 胞吐减少。SYT5-EGFP 的过表达增加了组胺诱导的 WPB 胞吐作用的速率和程度,并增加了 VWFpp 的分泌。表达钙结合缺陷的 SYT5 突变体 (SYT5-Asp197Ser-EGFP) 模拟了内源性 SYT5 的耗竭。我们确定 SYT5 是一种 WPB 相关的钙传感器,调节血管内皮细胞中储存介质的 Ca 依赖性分泌。