The molecular details of cytokine signaling via the JAK/STAT pathway

被引:689
作者
Morris, Rhiannon [1 ,2 ]
Kershaw, Nadia J. [1 ,2 ]
Babon, Jeffrey J. [1 ,2 ]
机构
[1] Walter & Eliza Hall Inst Med Res, 1G Royal Parade, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Dept Med Biol, Parkville, Vic 3050, Australia
基金
英国医学研究理事会;
关键词
cytokine; Cytokine Signaling; JAK/STAT; SOCS; cytokine receptor; hematopoiesis; PROTEIN-TYROSINE-PHOSPHATASE; LEUKEMIA-INHIBITORY FACTOR; MICE LACKING SUPPRESSOR; INTERFERON-ALPHA RECEPTOR; GENOME-WIDE ANALYSIS; CRYSTAL-STRUCTURE; PSEUDOKINASE-DOMAIN; STRUCTURAL BASIS; GROWTH-HORMONE; DNA-BINDING;
D O I
10.1002/pro.3519
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
More than 50 cytokines signal via the JAK/STAT pathway to orchestrate hematopoiesis, induce inflammation and control the immune response. Cytokines are secreted glycoproteins that act as intercellular messengers, inducing proliferation, differentiation, growth, or apoptosis of their target cells. They act by binding to specific receptors on the surface of target cells and switching on a phosphotyrosine-based intracellular signaling cascade initiated by kinases then propagated and effected by SH2 domain-containing transcription factors. As cytokine signaling is proliferative and often inflammatory, it is tightly regulated in terms of both amplitude and duration. Here we review molecular details of the cytokine-induced signaling cascade and describe the architectures of the proteins involved, including the receptors, kinases, and transcription factors that initiate and propagate signaling and the regulatory proteins that control it.
引用
收藏
页码:1984 / 2009
页数:26
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