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趋化因子受体CCR5:对其结构、功能及调控的深入了解

Chemokine receptor CCR5: insights into structure, function, and regulation.

作者信息

Oppermann Martin

机构信息

Department of Immunology, Georg-August-University Göttingen, Kreuzbergring 57, 37075, Germany.

出版信息

Cell Signal. 2004 Nov;16(11):1201-10. doi: 10.1016/j.cellsig.2004.04.007.

Abstract

CC chemokine receptor 5 (CCR5) is a seven-transmembrane, G protein-coupled receptor (GPCR) which regulates trafficking and effector functions of memory/effector T-lymphocytes, macrophages, and immature dendritic cells. It also serves as the main coreceptor for the entry of R5 strains of human immunodeficiency virus (HIV-1, HIV-2). Chemokine binding to CCR5 leads to cellular activation through pertussis toxin-sensitive heterotrimeric G proteins as well as G protein-independent signalling pathways. Like many other GPCR, CCR5 is regulated by agonist-dependent processes which involve G protein coupled receptor kinase (GRK)-dependent phosphorylation, beta-arrestin-mediated desensitization and internalization. This review discusses recent advances in the elucidation of the structure and function of CCR5, as well as the complex mechanisms that regulate CCR5 signalling and cell surface expression.

摘要

C-C趋化因子受体5(CCR5)是一种七跨膜G蛋白偶联受体(GPCR),可调节记忆/效应T淋巴细胞、巨噬细胞和未成熟树突状细胞的运输及效应功能。它也是人类免疫缺陷病毒(HIV-1、HIV-2)R5毒株进入细胞的主要共受体。趋化因子与CCR5结合会通过百日咳毒素敏感的异源三聚体G蛋白以及不依赖G蛋白的信号通路导致细胞活化。与许多其他GPCR一样,CCR5受激动剂依赖性过程调节,这些过程涉及G蛋白偶联受体激酶(GRK)依赖性磷酸化、β-抑制蛋白介导的脱敏和内化。本文综述了CCR5结构与功能解析方面的最新进展,以及调节CCR5信号传导和细胞表面表达的复杂机制。

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