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RhoB-Dependent Modulation of Postendocytic Traffic in Polarized Madin-Darby Canine Kidney Cells

机译:RhoB依赖的极化麦丁达比犬肾脏细胞内吞后交通。

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The Rho family of GTPases is implicated in the control of endocytic and biosynthetic traffic of many cell types; however, the cellular distribution of RhoB remains controversial and its function is not well understood. Using confocal microscopy, we found that endogenous RhoB and green fluorescent protein-tagged wild-type RhoB were localized to early endosomes, and to a much lesser extent to recycling endosomes, late endosomes or Golgi complex of fixed or live polarized Madin-Darby canine kidney cells. Consistent with RhoB localization to early endosomes, we observed that expression of dominant-negative RhoBN19 or dominant-active RhoBV14 altered postendocytic traffic of ligand-receptor complexes that undergo recycling, degradation or transcytosis. In vitro assays established that RhoB modulated the basolateral-to-apical transcytotic pathway by regulating cargo exit from basolateral early endosomes. Our results indicate that RhoB is localized, in part, to early endosomes where it regulates receptor egress through the early endocytic system.
机译:GTPases的Rho家族与许多细胞类型的内吞和生物合成运输有关。然而,RhoB的细胞分布仍存在争议,其功能尚不清楚。使用共聚焦显微镜,我们发现内源性RhoB和带有绿色荧光蛋白标签的野生型RhoB定位于早期内体,而循环利用内体,晚期内体或固定或存活的极化Madin-Darby犬肾的高尔基复合体的程度要小得多。细胞。与早期体内核糖体的RhoB定位一致,我们观察到显性负性RhoBN19或显性活性RhoBV14的表达改变了配体-受体复合物的内吞后运输,配体-受体复合物经历了再循环,降解或胞吞作用。体外测定表明,RhoB通过调节基底外侧早期内体的货物出口来调节基底外侧到顶端的胞吞途径。我们的结果表明,RhoB部分定位于早期的内体,在该内体中它通过早期的内吞系统调节受体的流出。

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