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膜蛋白通过极化的Caco-2细胞的共同顶端内体区室进行运输。

Membrane protein trafficking through the common apical endosome compartment of polarized Caco-2 cells.

作者信息

Knight A, Hughson E, Hopkins C R, Cutler D F

机构信息

Medical Research Council Laboratory for Molecular Cell Biology, University College, London.

出版信息

Mol Biol Cell. 1995 May;6(5):597-610. doi: 10.1091/mbc.6.5.597.

Abstract

By raising monoclonal antibodies to the apical surface of Caco-2 cells we have identified a membrane protein (p100) that internalizes and recycles constitutively between the apical plasma membrane and endosomes in the apical cytoplasm. By applying tracers bound to the transferrin receptor, which internalizes and recycles back to the basolateral border, we demonstrate that the apical endosomes containing p100 include a subset of multivesticular bodies (MVB), which are also accessible to proteins arriving from the basolateral endosome. Tracers bound to EGF receptors and alpha-2-macroglobulin, which internalize from the basolateral border and are degraded, probably in lysosomes, also pass through the p100-containing MVB. These studies therefore suggest that the apical cytoplasm of Caco-2 cells contains a population of MVB capable of receiving membrane proteins trafficking in from both apical and basolateral borders and then routing them to a variety of cell surface and intracellular destinations. The differential distribution of apical and basolateral tracers within the 50-nm-diameter tubules connected to these p100-positive apical MVB suggests that the destination of proteins trafficking from the MVB back to apical and basolateral surfaces is determined by the tubules to which they gain access.

摘要

通过制备针对Caco-2细胞顶端表面的单克隆抗体,我们鉴定出一种膜蛋白(p100),它在顶端质膜和顶端细胞质中的内体之间持续内化和循环。通过应用与转铁蛋白受体结合的示踪剂,转铁蛋白受体会内化并循环回到基底外侧边界,我们证明含有p100的顶端内体包括多囊泡体(MVB)的一个亚群,来自基底外侧内体的蛋白质也可进入这些多囊泡体。与表皮生长因子受体和α-2-巨球蛋白结合的示踪剂,它们从基底外侧边界内化并可能在溶酶体中降解,也会穿过含有p100的MVB。因此,这些研究表明,Caco-2细胞的顶端细胞质含有一群MVB,它们能够接收从顶端和基底外侧边界运输进来的膜蛋白,然后将它们导向各种细胞表面和细胞内目的地。与这些p100阳性顶端MVB相连的直径50纳米的小管内顶端和基底外侧示踪剂的差异分布表明,从MVB运输回顶端和基底外侧表面的蛋白质的目的地是由它们进入的小管决定的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ccb/301218/cd60750eb428/mbc00074-0121-a.jpg

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