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Phase coexistence and connectivity in the apical membrane of polarized epithelial cells

机译:极化上皮细胞顶膜中的相位共存和连通性

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Although it is well described in model membranes, little is known about phase separation in biological membranes. Here, we provide evidence for a coexistence of at least two different lipid bilayer phases in the apical plasma membrane of epithelial cells. Phase connectivity was assessed by measuring long-range diffusion of several membrane proteins by fluorescence recovery after photo-bleaching in two polarized epithelial cell lines and one fibroblast cell line. In contrast to the fibroblast plasma membrane, in which all of the proteins diffused with similar characteristics, in the apical membrane of epithelial cells the proteins could be divided into two groups according to their diffusion characteristics. At room temperature ( ≈ 25℃), one group showed fast diffusion and complete recovery. The other diffused three to four times slower and, more importantly, displayed only partial recovery. Only the first group comprises proteins that are believed to be associated with lipid rafts. The partial recovery is not caused by topological constraints (microvilli, etc.), cytoskeletal constraints, or protein-protein interactions, because all proteins show 100% recovery in fluorescence recovery after photobleaching experiments at 37℃. In addition, the raft-associated proteins cannot be coclustered by antibodies on the apical membrane at 12℃. The interpretation that best fits these data is that the apical membrane of epithelial cells is a phase-separated system with a continuous (percolating) raft phase < 25℃ in which isolated domains of the nonraft phase are dispersed, whereas at 37℃ the nonraft phase becomes the continuous phase with isolated domains of the raft phase dispersed in it.
机译:尽管在模型膜中已有很好的描述,但对于生物膜中的相分离知之甚少。在这里,我们提供了上皮细胞顶质膜中至少两个不同的脂质双层相共存的证据。在两个极化的上皮细胞系和一个成纤维细胞系中进行光漂白后,通过荧光恢复测量几种膜蛋白的远距离扩散来评估相连接性。与成纤维细胞质膜(其中所有蛋白质均以相似的特性扩散)相反,在上皮细胞的顶膜中,根据其扩散特性,蛋白质可分为两组。在室温(≈25℃)下,一组显示出快速扩散并完全恢复。另一个扩散速度慢了三到四倍,更重要的是,仅显示出部分恢复。仅第一组包含被认为与脂质筏相关的蛋白质。部分回收不是由拓扑约束(微绒毛等),细胞骨架约束或蛋白质-蛋白质相互作用引起的,因为在37℃的光漂白实验后,所有蛋白质在荧光回收中均显示100%的回收。此外,在12℃下,与筏相关的蛋白质不能被顶膜上的抗体结合。最适合这些数据的解释是上皮细胞的顶膜是一个相分离的系统,具有连续的(渗流)筏相<25℃,其中非筏相的分离域分散,而在37℃时非筏相变成连续相,其中筏相的隔离域分散在其中。

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