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内吞再循环的定性和定量分析

Qualitative and quantitative analysis of endocytic recycling.

作者信息

Reineke James B, Xie Shuwei, Naslavsky Naava, Caplan Steve

机构信息

Department of Biochemistry and Molecular Biology and the Fred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE, USA.

出版信息

Methods Cell Biol. 2015;130:139-55. doi: 10.1016/bs.mcb.2015.04.002. Epub 2015 Jun 11.

Abstract

Endocytosis, which encompasses the internalization and sorting of plasma membrane (PM) lipids and proteins to distinct membrane-bound intracellular compartments, is a highly regulated and fundamental cellular process by which eukaryotic cells dynamically regulate their PM composition. Indeed, endocytosis is implicated in crucial cellular processes that include proliferation, migration, and cell division as well as maintenance of tissue homeostasis such as apical-basal polarity. Once PM constituents have been taken up into the cell, either via clathrin-dependent endocytosis (CDE) or clathrin-independent endocytosis (CIE), they typically have two fates: degradation through the late-endosomal/lysosomal pathway or returning to the PM via endocytic recycling pathways. In this review, we will detail experimental procedures that allow for both qualitative and quantitative assessment of endocytic recycling of transmembrane proteins internalized by CDE and CIE, using the HeLa cervical cancer cell line as a model system.

摘要

内吞作用包括将质膜(PM)脂质和蛋白质内化并分选到不同的膜结合细胞内区室,是一个高度受调控的基本细胞过程,真核细胞通过该过程动态调节其质膜组成。实际上,内吞作用涉及关键的细胞过程,包括增殖、迁移和细胞分裂,以及维持组织稳态,如顶端-基部极性。一旦质膜成分通过网格蛋白依赖性内吞作用(CDE)或网格蛋白非依赖性内吞作用(CIE)被细胞摄取,它们通常有两种命运:通过晚期内体/溶酶体途径降解,或通过内吞循环途径返回质膜。在本综述中,我们将详细介绍实验程序,该程序可以使用HeLa宫颈癌细胞系作为模型系统,对通过CDE和CIE内化的跨膜蛋白的内吞循环进行定性和定量评估。

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