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首页> 外文期刊>Molecular biology of the cell >Endocytosed Cation-Independent Mannose 6-Phosphate Receptor Traffics via the Endocytic Recycling Compartment en Route to the trans-Golgi Network and a Subpopulation of Late Endosomes
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Endocytosed Cation-Independent Mannose 6-Phosphate Receptor Traffics via the Endocytic Recycling Compartment en Route to the trans-Golgi Network and a Subpopulation of Late Endosomes

机译:通过内吞再循环室的内吞细胞阳离子独立的甘露糖6-磷酸受体运输途中到反高尔基网络和后期的内体亚群。

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摘要

Although the distribution of the cation-independent mannose 6-phosphate receptor (CI-MPR) has been well studied, its intracellular itinerary and trafficking kinetics remain uncertain. In this report, we describe the endocytic trafficking and steady-state localization of a chimeric form of the CI-MPR containing the ecto-domain of the bovine CI-MPR and the murine transmembrane and cytoplasmic domains expressed in a CHO cell line. Detailed confocal microscopy analysis revealed that internalized chimeric CI-MPR overlaps almost completely with the endogenous CI-MPR but only partially with individual markers for the trans -Golgi network or other endosomal compartments. After endocytosis, the chimeric receptor first enters sorting endosomes, and it then accumulates in the endocytic recycling compartment. A large fraction of the receptors return to the plasma membrane, but some are delivered to the trans -Golgi network and/or late endosomes. Over the course of an hour, the endocytosed receptors achieve their steady-state distribution. Importantly, the receptor does not start to colocalize with late endosomal markers until after it has passed through the endocytic recycling compartment. In CHO cells, only a small fraction of the receptor is ever detected in endosomes bearing substrates destined for lysosomes (kinetically defined late endosomes). These data demonstrate that CI-MPR takes a complex route that involves multiple sorting steps in both early and late endosomes.
机译:尽管已经很好地研究了不依赖阳离子的甘露糖6-磷酸受体(CI-MPR)的分布,但其细胞内行程和运输动力学仍然不确定。在此报告中,我们描述了包含牛CI-MPR的胞外域以及在CHO细胞系中表达的鼠跨膜和胞质域的CI-MPR嵌合形式的内吞运输和稳态定位。详细的共聚焦显微镜分析显示,内化的嵌合CI-MPR与内源CI-MPR几乎完全重叠,但与反式-高尔基体网络或其他内体区室的单个标记仅部分重叠。内吞后,嵌合受体首先进入分选的内体,然后在内吞回收区积累。大部分受体返回质膜,但有些则被传递至反-高尔基体网络和/或晚期内体。在一个小时的过程中,内吞的受体达到了稳态分布。重要的是,该受体直到其通过内吞循环室后才开始与后期的内体标记物共定位。在CHO细胞中,在携带有溶酶体底物的内体中(在动力学上定义为晚期内体),仅检测到一小部分受体。这些数据表明,CI-MPR采用复杂的途径,涉及早期和晚期内体的多个分选步骤。

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