Suppressor of cytokine signaling-1 is an IL-4-inducible gene in macrophages and feedback inhibits IL-4 signaling

被引:68
作者
Dickensheets, H.
Vazquez, N.
Sheikh, F.
Gingras, S.
Murray, P. J.
Ryan, J. J.
Donnelly, R. P.
机构
[1] US FDA, Div Therapeut Prot, Ctr Drug Evaluat & Res, Rockville, MD 20852 USA
[2] St Jude Childrens Res Hosp, Dept Biochem, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Infect Dis, Memphis, TN 38105 USA
[4] Virginia Commonwealth Univ, Dept Biol, Richmond, VA 23284 USA
关键词
SOCS; STAT6; macrophages; interleukin-4;
D O I
10.1038/sj.gene.6364352
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Interferon-gamma and interleukin-4 (IL-4) induce distinct gene expression profiles in macrophages by differentially activating signal transducers and activators of transcription ( STAT) 1 and STAT6, respectively. The role of suppressor of cytokine signaling (SOCS)-1 as a negative regulator of IFN-gamma signaling is well established. However, its potential role as a negative regulator of IL-4 signaling has not been explored. We found that IL-4, like IFN-gamma, induces rapid de novo expression of SOCS-1 in primary macrophages. Induction of SOCS-1 gene expression by IL-4 is STAT6- dependent, whereas induction of SOCS-1 by IFN-gamma is STAT1-dependent. Unlike their common ability to induce expression of SOCS-1, IL-4 also induced expression of SOCS-2 but not SOCS-3 in macrophages, whereas IFN-gamma induced expression of SOCS-3 but not SOCS-2. Forced expression of SOCS-1 or SOCS-3, but not SOCS-2, inhibited activation of STAT6 by IL-4. Moreover, SOCS-1 appears to serve as an endogenous regulator of IL-4 signaling in macrophages because the magnitude and duration of STAT6 activation as well as IL-4-mediated gene expression were much greater in SOCS-1-deficient (SOCS-1(-/-)) macrophages than in wild-type macrophages. Our findings demonstrate that, like IFN-gamma, IL-4 also induces expression of SOCS-1 in macrophages, and SOCS-1 feedback inhibits expression of STAT6- responsive genes.
引用
收藏
页码:21 / 27
页数:7
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