Suppressor of cytokine signaling-1 selectively inhibits LPS-induced IL-6 production by regulating JAK-STAT

被引:145
作者
Kimura, A
Naka, T
Muta, T
Takeuchi, O
Akira, S
Kawase, I
Kishimoto, T
机构
[1] Osaka Univ, Microbial Dis Res Inst, Lab Immune Regulat, Grad Sch Frontier Biosci, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Microbial Dis Res Inst, Dept Mol Med, Grad Sch Med, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Microbial Dis Res Inst, Dept Host Defense, Suita, Osaka 5650871, Japan
[4] Kyushu Univ, Grad Sch Med Sci, Dept Mol & Cellular Biochem, Fukuoka 8128582, Japan
关键词
innate immunity; JAK2; STAT5; toll-like receptor signal;
D O I
10.1073/pnas.0508517102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Suppressor of cytokine signaling-1 (SOCS-1) is one of the negative-feedback regulators of Janus kinase (JAK)-signal transducer and activator of transcription (STAT) signaling. We previously showed that SOCS-1 participates in LPS signaling, but it is not entirely clear yet how SOCS-1 suppresses LPS signaling. In this study, we demonstrate that SOCS-1 selectively inhibits LPS-induced IL-6 production through regulation of JAK-STAT but not production of TNF-alpha, granulocyte colony-stimulating factor, IFN-beta, and other cytokines. We found that LPS directly activated Jak2 and Stat5, whereas SOCS-1 inhibited LPS-induced Jak2 and Stat5 activation. Furthermore, AG490, a Jak-specific inhibitor, and dominant negative Stat5 only reduced LPS-induced IL-6 production. Additionally, Stat5 interacted with p50, resulting in recruitment of Stat5 to the IL-6 promoter together with p50 in response to LPS stimulation. These findings suggest that the JAK-STAT pathway participates in LPS-induced IL-6 production and that SOCS-1 suppresses LIPS signaling by regulating JAK-STAT.
引用
收藏
页码:17089 / 17094
页数:6
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