Inhibition of IL-6 family cytokines by SOCS3

被引:215
作者
Babon, Jeffrey J. [1 ,2 ]
Varghese, Leila N. [1 ,2 ]
Nicola, Nicos A. [1 ,2 ]
机构
[1] Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
[2] Univ Melbourne, Parkville, Vic 3052, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会; 澳大利亚国家健康与医学研究理事会; 美国国家卫生研究院;
关键词
IL-6; Janus Kinases; SOCS; Cytokine signalling; JAK/STAT; TYROSINE KINASE-ACTIVITY; MICE LACKING SUPPRESSOR; INDUCIBLE SH2 PROTEIN; EMBRYONIC STEM-CELLS; SIGNAL-TRANSDUCTION; CRYSTAL-STRUCTURE; UBIQUITIN LIGASE; INSULIN-RECEPTOR; GROWTH-HORMONE; ERYTHROPOIETIN RECEPTOR;
D O I
10.1016/j.smim.2013.12.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
IL-6 a multi-functional cytokine with important effects in both inflammation and haematopoiesis. SOCS3 is the primary inhibitor of IL-6 signalling, interacting with gp130, the common shared chain of the IL-6 family of cytokines, and JAK1, JAK2 and TYK2 to control both the duration of signalling and the biological response. Recent biochemical and structural studies have shown SOCS3 binds to only these three JAKs, all of which are associated with IL-6 signalling, and not JAK3. This specificity is determined by a three residue "GQM" motif in the kinase domain of JAK1, JAK2 and TYK2. SOCS3 binds to JAK and gp130 simultaneously, and inhibits JAM activity in an ATP-independent manner by partially occluding the kinase's substrate binding groove with its kinase inhibitory region. We therefore propose a model in which each of gp130, JAM and SOCS3 are directly bound to the other two, allowing SOCS3 to inhibit IL6 signalling with high potency and specificity. Crown Copyright (C) 2014 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:13 / 19
页数:7
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