凝胶素控制着血小板中磷脂酰丝氨酸(PS)阳性微囊泡(MV)的释放。

IF 4.4 2区 生物学 Q2 CELL BIOLOGY Cellular signalling Pub Date : 2024-09-24 DOI:10.1016/j.cellsig.2024.111433
Manoj Paul , Felix Hong , Hervé Falet , Hugh Kim
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引用次数: 0

摘要

血小板被血管损伤或细胞外激动剂激活后,会迅速改变形状,这一过程受肌动蛋白细胞骨架和附属蛋白的调节。伴随血小板形状改变的是其细胞内颗粒分泌止血因子和免疫调节细胞因子,以及释放含有促炎细胞因子和促凝血剂磷脂酰丝氨酸(PS)的微囊泡(MV)。然而,肌动蛋白动力学在 MV 生成中的作用仍不清楚。在这项研究中,我们发现用细胞松弛素 D 阻断肌动蛋白聚合可减轻凝血酶或钙离子诱导剂 A23187 刺激的人血小板中 PS 阳性 MV 的释放。肌动蛋白分裂蛋白凝胶溶蛋白(Gsn)能促进活化血小板中肌动蛋白丝的正常周转。与对照组小鼠的血小板相比,Gsn缺陷(Gsn-/-)小鼠的血小板显示出MV释放减少。这些研究结果表明,肌动蛋白细胞骨架的正常动态对血小板中中微粒的生成至关重要,这对血小板的促炎和促凝血功能有影响。
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Gelsolin controls the release of phosphatidylserine (PS)-positive microvesicles (MVs) from platelets
Upon activation by vascular injury or extracellular agonists, platelets undergo rapid change shape, a process regulated by the actin cytoskeleton and accessory proteins. Platelet shape change is accompanied by the secretion of hemostatic factors and immunomodulatory cytokines from their intracellular granules, as well as the release of microvesicles (MVs) containing pro-inflammatory cytokines and procoagulant phosphatidylserine (PS). However, the role of actin dynamics in MV generation remains unclear. In this study, we found that blocking actin polymerization with cytochalasin D attenuated the release of PS-positive MVs in human platelets stimulated by thrombin or the calcium ionophore A23187. The actin-severing protein gelsolin (Gsn) facilitates normal actin filament turnover in activated platelets. Platelets from Gsn-deficient (Gsn−/−) mice showed reduced MV release compared to platelets from control mice. These findings indicate that the proper dynamics of the actin cytoskeleton are essential for MV generation in platelets, which has implications for their pro-inflammatory and procoagulant functions.
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来源期刊
Cellular signalling
Cellular signalling 生物-细胞生物学
CiteScore
8.40
自引率
0.00%
发文量
250
审稿时长
27 days
期刊介绍: Cellular Signalling publishes original research describing fundamental and clinical findings on the mechanisms, actions and structural components of cellular signalling systems in vitro and in vivo. Cellular Signalling aims at full length research papers defining signalling systems ranging from microorganisms to cells, tissues and higher organisms.
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