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Localization of VE-cadherin in plasmalemmal cholesterol rich microdomains and the effects of cholesterol depletion on VE-cadherin mediated cell-cell adhesion

机译:VE-钙粘着蛋白在血浆中富含胆固醇的微区中的定位以及胆固醇耗竭对VE-钙粘着蛋白介导的细胞粘附的影响

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VE-cadherin is the predominant adhesion molecule in vascular endothelial cells being responsible for maintenance of the endothelial barrier function by forming adhesive contacts (adherens junctions) to neighbouring cells. We found by use of single molecule fluorescence microscopy that VE-cadherin is localised in preformed clusters when not inside adherens junctions. These clusters depend on the integrity of the actin cytoskeleton and are localised in cholesterol rich microdomains of mature endothelial cells as found by membrane fractionation. The ability to form and maintain VE-cadherin based junctions was probed using the laser tweezer technique, and we found that cholesterol depletion has dramatical effects on VE-cadherin mediated adhesion. While a 30% reduction of the cholesterol-level results in an increase of adhesion, excessive cholesterol depletion by about 60% leads to an almost complete loss of VE-cadherin function. Nevertheless, the cadherin concentration in the membrane and the single molecule kinetic parameters of the cadherin are not changed. Our results suggest that the actin cytoskeleton, junction-associated proteins and protein-lipid assemblies in cholesterol-rich microdomains mutually stabilise each other to form functional adhesion contacts. (C) 2014 Elsevier B.V. All rights reserved.
机译:VE-钙粘着蛋白是血管内皮细胞中的主要粘附分子,负责通过与邻近细胞形成粘附性接触(粘附连接)来维持内皮屏障功能。通过使用单分子荧光显微镜,我们发现VE-钙粘着蛋白位于粘附簇结内时位于局部簇中。这些簇取决于肌动蛋白细胞骨架的完整性,并且位于成熟内皮​​细胞的富含胆固醇的微区中,如通过膜分离所发现的。使用激光镊子技术探讨了形成和维持基于VE-钙黏着蛋白的连接的能力,并且我们发现胆固醇的消耗对VE-钙黏着蛋白介导的粘附具有显着影响。胆固醇水平降低30%会导致粘连增加,而胆固醇过度消耗约60%会导致VE-钙粘蛋白功能几乎完全丧失。然而,膜中的钙黏着蛋白浓度和钙黏着蛋白的单分子动力学参数没有改变。我们的研究结果表明,富含胆固醇的微区中的肌动蛋白细胞骨架,连接相关蛋白和蛋白-脂质组装体相互稳定,形成功能性粘附接触。 (C)2014 Elsevier B.V.保留所有权利。

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