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趋化因子受体的内吞转运。

Endocytic trafficking of chemokine receptors.

机构信息

Department of Pharmacology, Health Sciences Division, Loyola University Chicago, Maywood, IL 60153, United States.

出版信息

Curr Opin Cell Biol. 2014 Apr;27:72-7. doi: 10.1016/j.ceb.2013.11.011. Epub 2013 Dec 14.

Abstract

Chemokine receptors belong to the super family of G protein-coupled receptors (GPCRs). The cognate ligands for chemokine receptors are small circulating proteins known as chemokines. Upon binding to their cognate chemokines, receptors are rapidly desensitized, internalized onto early endosomes and sorted either into a recycling pathway or degradative pathway. Chemokine receptor trafficking is essential because it limits the magnitude and duration of signaling by removing receptors from the cell surface thereby limiting access to their ligands, but it also delivers bound chemokines to lysosomes for degradation. Receptor sorting into the recycling pathway contributes to resensitization of receptor signaling, whereas sorting into the degradative pathway leads to long-term attenuation of signaling. Recent studies have revealed some key information regarding the molecular determinants mediating chemokine receptor internalization and have shed light on the mechanisms dictating sorting into either the recycling or degradative pathways. Here I discuss our current understanding of the mechanisms mediating chemokine receptor trafficking with a focus primarily on recent findings for the chemokine receptor CXCR4.

摘要

趋化因子受体属于 G 蛋白偶联受体 (GPCRs) 的超家族。趋化因子受体的同源配体是已知的小循环蛋白趋化因子。与同源趋化因子结合后,受体迅速脱敏,被内吞到早期内体,并被分拣到再循环途径或降解途径。趋化因子受体的运输是必不可少的,因为它通过从细胞表面去除受体来限制信号的幅度和持续时间,从而限制了对其配体的获取,但它也将结合的趋化因子递送到溶酶体进行降解。受体再循环途径的分拣有助于受体信号的重新敏化,而分拣到降解途径则导致信号的长期衰减。最近的研究揭示了一些关于介导趋化因子受体内化的分子决定因素的关键信息,并阐明了决定分拣到再循环或降解途径的机制。在这里,我主要讨论我们对介导趋化因子受体运输的机制的理解,重点是最近关于趋化因子受体 CXCR4 的发现。

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