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Revealing the Topography of Cellular Membrane Domains by Combined Atomic Force Microscopy/Fluorescence Imaging

机译:结合原子力显微镜/荧光成像揭示细胞膜结构域的地形

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摘要

Simultaneous atomic force microscopy (AFM) and confocal fluorescence imaging were used to observe in aqueous buffer the three-dimensional landscape of the inner surface of membrane sheets stripped from fixed tumor mast cells. The AFM images reveal prominent, irregularly shaped raised domains that label with fluorescent markers for both resting and activated immunoglobin E receptors (FcɛRI), as well as with cholera toxin-aggregated GM1 and clathrin. The latter suggests that coated pits bud from these regions. These features are interspersed with flatter regions of membrane and are frequently surrounded and interconnected by cytoskeletal assemblies. The raised domains shrink in height by ∼50% when cholesterol is extracted with methyl-β-cyclodextrin. Based on composition, the raised domains seen by AFM correspond to the cholesterol-enriched dark patches observed in transmission electron microscopy (TEM). These patches were previously identified as sites of signaling and endocytosis based on their localization of activated FcɛRI, at least 10 associated signaling molecules, and the presence of clathrin-coated pits. Overall the data suggest that signaling and endocytosis occur in mast cells from raised membrane regions that depend on cholesterol for their integrity and may be organized in specific relationship with the cortical cytoskeleton.
机译:同时原子力显微镜(AFM)和共聚焦荧光成像用于在水性缓冲液中观察从固定的肿瘤肥大细胞剥离的膜片内表面的三维景观。 AFM图像显示突出的,不规则形状的凸起结构域,该结构域用荧光标记标记静止和激活的免疫球蛋白E受体(FcɛRI),以及霍乱毒素聚集的GM1和网格蛋白。后者表明涂层凹坑从这些区域萌芽。这些特征散布着较平坦的膜区域,并经常被细胞骨架组件包围和互连。当用甲基-β-环糊精提取胆固醇时,凸起的结构域高度缩小约50%。基于组成,AFM看到的凸起结构域对应于在透射电子显微镜(TEM)中观察到的富含胆固醇的深色斑块。根据它们在活化的FcɛRI的定位,至少10个相关的信号分子以及网格蛋白包被的凹坑的存在,先前将这些补丁鉴定为信号传导和胞吞作用的位点。总体而言,数据表明肥大细胞中的信号传导和内吞作用发生在依赖于胆固醇完整性的升高的膜区域,并且可能与皮质细胞骨架有特定的关系。

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