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Regulation of desmosome assembly in MDCK epithelial cells: coordination of membrane core and cytoplasmic plaque domain assembly at the plasma membrane

机译:MDCK上皮细胞中桥粒组装的调节:质膜上的膜核心和细胞质斑块域组装的协调

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摘要

Desmosomes are major components of the intercellular junctional complex in epithelia. They consist of at least eight different cytoplasmic and integral membrane proteins that are organized into two biochemically and structurally distinct domains: the cytoplasmic plaque and membrane core. We showed previously that in MDCK epithelial cells major components of the cytoplasmic plaque (desmoplakin I and II; DPI/II) and membrane core domains (desmoglein I; DGI) initially enter a pool of proteins that is soluble in buffers containing Triton X-100, and then titrate into an insoluble pool before their arrival at the plasma membrane (Pasdar, M., and W. J. Nelson. 1988. J. Cell Biol. 106:677- 685; Pasdar. M., and W. J. Nelson. 1989. J. Cell Biol. 109:163-177). We have now examined whether either the soluble or insoluble pool of these proteins represents an intracellular site for assembly and interactions between the domains before their assembly into desmosomes at the plasma membrane. Interactions between the Triton X-100-soluble pools of DPI/II and DGI were analyzed by sedimentation of extracted proteins in sucrose gradients. Results show distinct differences in the sedimentation profiles of these proteins, suggesting that they are not associated in the Triton X-100-soluble pool of proteins; this was also supported by the observation that DGI and DPI/II could not be coimmunoprecipitated in a complex with each other from sucrose gradient fractions. Immunofluorescence analysis of the insoluble pools of DPI/II and DGI, in cells in which desmosome assembly had been synchronized, showed distinct differences in the spatial distributions of these proteins. Furthermore, DPI/II and DGI were found to be associated with different elements of cytoskeleton; DPI/II were located along cytokeratin intermediate filaments, whereas DGI appeared to be associated with microtubules. The regulatory role of cytoskeletal elements in the intracellular organization and assembly of the cytoplasmic plaque and membrane core domains, and their integration into desmosomes on the plasma membrane is discussed.
机译:桥粒是上皮细胞间连接复合物的主要成分。它们由至少八种不同的细胞质和整合膜蛋白组成,这些蛋白被组织成两个在生化和结构上不同的域:细胞质斑块和膜核心。先前我们表明,在MDCK上皮细胞中,细胞质斑块的主要成分(去粘蛋白I和II; DPI / II)和膜核心结构域(去粘蛋白I; DGI)最初进入的蛋白质池可溶于含Triton X-100的缓冲液中,然后滴定到不溶性溶液中,然后到达质膜(Pasdar,M.和WJ Nelson。1988. J. Cell Biol。106:677-685; Pasdar。M.和WJ Nelson。1989. J. (Cell Biol.109:163-177)。现在我们已经检查了这些蛋白质的可溶或不可溶池是否代表细胞内的组装位点,以及在结构域组装成质膜上的桥粒之前这些结构域之间的相互作用。通过在蔗糖梯度中沉淀提取的蛋白质来分析DPI / II和DGI的Triton X-100可溶性库之间的相互作用。结果显示这些蛋白质的沉降曲线存在明显差异,这表明它们与Triton X-100可溶性蛋白质库无关。这也得到以下观察结果的支持:DGI和DPI / II无法通过蔗糖梯度馏分彼此复合形成共免疫沉淀。在已经进行了桥粒组装的细胞中,对DPI / II和DGI的不溶池进行的免疫荧光分析表明,这些蛋白质的空间分布存在明显差异。此外,发现DPI / II和DGI与细胞骨架的不同元素有关。 DPI / II位于细胞角蛋白中间丝,而DGI似乎与微管有关。讨论了细胞骨架成分在细胞内斑块和膜核心结构域的细胞内组织和组装中的调节作用,以及它们整合到质膜上的桥粒中的作用。

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