SOCS3
JAK-STAT信号通路
Janus激酶1
细胞因子信号抑制因子1
细胞因子受体
细胞因子信号抑制因子
SOCS5型
受体
细胞生物学
生物
斯达
SOCS6系列
细胞因子
贾纳斯激酶
SOCS2
信号转导
状态4
STAT1
STAT蛋白
状态5
癌症研究
车站3
Janus激酶2
细胞信号
磷酸化
免疫学
抑制器
基因
受体酪氨酸激酶
遗传学
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2007-03-01
卷期号:178 (5): 2623-2629
被引量:1028
标识
DOI:10.4049/jimmunol.178.5.2623
摘要
Abstract Universal and essential to cytokine receptor signaling, the JAK-STAT pathway is one of the best understood signal transduction cascades. Almost 40 cytokine receptors signal through combinations of four JAK and seven STAT family members, suggesting commonality across the JAK-STAT signaling system. Despite intense study, there remain substantial gaps in understanding how the cascades are activated and regulated. Using the examples of the IL-6 and IL-10 receptors, I will discuss how diverse outcomes in gene expression result from regulatory events that effect the JAK1-STAT3 pathway, common to both receptors. I also consider receptor preferences by different STATs and interpretive problems in the use of STAT-deficient cells and mice. Finally, I consider how the suppressor of cytokine signaling (SOCS) proteins regulate the quality and quantity of STAT signals from cytokine receptors. New data suggests that SOCS proteins introduce additional diversity into the JAK-STAT pathway by adjusting the output of activated STATs that alters downstream gene activation.
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