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Sorting nexin 27 regulates basal and stimulated brush border trafficking of NHE3

机译:排序nexin 27调节NHE3的基础和刺激刷缘交易

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Sorting nexin 27 (SNX27) contains a PDZ domain that is phylogenetically related to the PDZ domains of the NHERF proteins. Studies on nonepithelial cells have shown that this protein is located in endosomes, where it regulates trafficking of cargo proteins in a PDZ domain–dependent manner. However, the role of SNX27 in trafficking of cargo proteins in epithelial cells has not been adequately explored. Here we show that SNX27 directly interacts with NHE3 (C-terminus) primarily through the SNX27 PDZ domain. A combination of knockdown and reconstitution experiments with wild type and a PDZ domain mutant (GYGF → GAGA) of SNX27 demonstrate that the PDZ domain of SNX27 is required to maintain basal NHE3 activity and surface expression of NHE3 in polarized epithelial cells. Biotinylation-based recycling and degradation studies in intestinal epithelial cells show that SNX27 is required for the exocytosis (not endocytosis) of NHE3 from early endosome to plasma membrane. SNX27 is also required to regulate the retention of NHE3 on the plasma membrane. The findings of the present study extend our understanding of PDZ-mediated recycling of cargo proteins from endosome to plasma membrane in epithelial cells.
机译:分类神经毒素27(SNX27)包含与NHERF蛋白的PDZ域在系统发育上相关的PDZ域。对非上皮细胞的研究表明,该蛋白位于内体中,在那里以PDZ结构域依赖性方式调节货运蛋白的运输。然而,尚未充分探讨SNX27在上皮细胞中货物蛋白运输中的作用。在这里,我们显示SNX27主要通过SNX27 PDZ域直接与NHE3(C末端)相互作用。结合野生型和SNX27的PDZ域突变体(GYGF→GAGA)进行的敲除和重组实验的组合表明,需要SNX27的PDZ域来维持基础NHE3活性和极化上皮细胞中NHE3的表面表达。对肠道上皮细胞进行基于生物素化的再循环和降解研究表明,SNX27是NHE3从早期内体到质膜的胞吐作用(而非内吞作用)所必需的。还需要SNX27来调节NHE3在质膜上的保留。本研究的发现扩展了我们对PDZ介导的货物蛋白从内体到上皮细胞质膜回收的理解。

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