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趋化因子受体网络的调控机制

Mechanisms of Regulation of the Chemokine-Receptor Network.

作者信息

Stone Martin J, Hayward Jenni A, Huang Cheng, E Huma Zil, Sanchez Julie

机构信息

Infection and Immunity Program, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.

Department of Biochemistry and Molecular Biology, Monash University, Clayton, VIC 3800, Australia.

出版信息

Int J Mol Sci. 2017 Feb 7;18(2):342. doi: 10.3390/ijms18020342.

Abstract

The interactions of chemokines with their G protein-coupled receptors promote the migration of leukocytes during normal immune function and as a key aspect of the inflammatory response to tissue injury or infection. This review summarizes the major cellular and biochemical mechanisms by which the interactions of chemokines with chemokine receptors are regulated, including: selective and competitive binding interactions; genetic polymorphisms; mRNA splice variation; variation of expression, degradation and localization; down-regulation by atypical (decoy) receptors; interactions with cell-surface glycosaminoglycans; post-translational modifications; oligomerization; alternative signaling responses; and binding to natural or pharmacological inhibitors.

摘要

趋化因子与其G蛋白偶联受体的相互作用在正常免疫功能期间促进白细胞迁移,并且是对组织损伤或感染的炎症反应的关键方面。本综述总结了趋化因子与趋化因子受体相互作用的主要细胞和生化调节机制,包括:选择性和竞争性结合相互作用;基因多态性;mRNA剪接变异;表达、降解和定位的变化;非典型(诱饵)受体的下调;与细胞表面糖胺聚糖的相互作用;翻译后修饰;寡聚化;替代信号反应;以及与天然或药理学抑制剂的结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fd4/5343877/22ef2be51c62/ijms-18-00342-g001.jpg

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