信号转导
细胞因子受体
细胞生物学
JAK-STAT信号通路
斯达
生物
酪氨酸磷酸化
细胞因子
SH2域
SOCS3
转录因子
SOCS5型
细胞因子信号抑制因子
糖蛋白130
酪氨酸激酶
基因
车站3
遗传学
作者
Robyn Starr,Tracy A. Willson,Elizabeth M. Viney,Leecia J. Murray,John R Rayner,Brendan J. Jenkins,Thomas J. Gonda,Warren S. Alexander,D Metcalf,Nicos A. Nicola,Douglas J. Hilton
出处
期刊:Nature
[Nature Portfolio]
日期:1997-06-26
卷期号:387 (6636): 917-921
被引量:2077
摘要
Cytokines are secreted proteins that regulate important cellular responses such as proliferation and differentiation1. Key events in cytokine signal transduction are well defined: cytokines induce receptor aggregation, leading to activation of members of the JAK family of cytoplasmic tyrosine kinases. In turn, members of theSTAT family of transcription factors are phosphorylated, dimerize and increase the transcription of genes with STAT recognition sites in their promoters1,2,3,4. Less is known of how cytokine signal transduction is switched off. We have cloned a complementary DNA encoding a protein SOCS-1, containing an SH2-domain, by its ability to inhibit the macrophage differentiation of M1 cells in response to interleukin-6. Expression of SOCS-1 inhibited both interleukin-6-induced receptor phosphorylation and STAT activation. We have also cloned two relatives of SOCS-1, named SOCS-2 and SOCS-3, which together with the previously described CIS (ref. 5) form a new family of proteins. Transcription of all four SOCS genes is increased rapidly in response to interleukin-6, in vitro and in vivo, suggesting they may act in a classic negative feedback loop to regulate cytokine signal transduction.
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