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PMID: 12591901 已发表 · ppublish 英语

A role of suppressor of cytokine signaling 3 (SOCS3/CIS3/SSI3) in CD28-mediated interleukin 2 production.

The Journal of experimental medicine ·第 197 卷 ·第 4 期 ·2003-03-20

Matsumoto Akira, Seki Yoh-ichi, Watanabe Ryosuke, Hayashi Katsuhiko, Johnston James A, Harada Yohsuke, Abe Ryo, Yoshimura Akihiko, Kubo Masato

摘要

Suppressor of cytokine signaling (SOCS)3 has been characterized as a negative feedback regulator in cytokine-mediated Janus kinase signal transducer and activator of transcription signaling. However, this study shows that T cells from transgenic mice expressing SOCS3 exhibit a significant reduction in interleukin (IL)-2 production induced by T cell receptor cross-linking when T cells are costimulated with CD28. Decreased protein expression in SOCS3(+/-) mice enhanced CD28-mediated IL-2 production, clearly indicating the correlation between expression level of SOCS3 and IL-2 production ability. The SOCS3 protein interacted with phosphorylated CD28 through its SH2 domain but not the kinase inhibitory region. In addition, a point mutation in the SOCS3 SH2 domain attenuated the inhibition of CD28 function in IL-2 promoter activation. Committed T helper (Th)2 cells exclusively expressed SOCS3 and production of Th2 cytokines, such as IL-4 and IL-5, was much less dependent on CD28 costimulation compared with interferon gamma and IL-2 production in Th1 cells. Consistent with this notion, the expression level of SOCS3 in early T cell activation influenced the ability of IL-2 production induced by CD28 costimulation. Therefore, the SOCS3 may play an alternative role in prohibiting excessive progression of CD28-mediated IL-2 production.

文献信息
期刊
The Journal of experimental medicine
期刊简称
J Exp Med
发表日期
2003-03-20
收录日期
2003-02-19
更新日期
2016-11-24
语言
英语
国家/地区
United States
NLM ID
2985109R
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