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细胞因子信号转导抑制因子1是巨噬细胞中一种白细胞介素4诱导基因,可反馈抑制白细胞介素4信号转导。

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

作者信息

Dickensheets H, Vazquez N, Sheikh F, Gingras S, Murray P J, Ryan J J, Donnelly R P

机构信息

Division of Therapeutic Proteins, Center for Drug Evaluation and Research, Food and Drug Administration, Bethesda, MD, USA.

出版信息

Genes Immun. 2007 Jan;8(1):21-7. doi: 10.1038/sj.gene.6364352. Epub 2006 Nov 9.

DOI:10.1038/sj.gene.6364352
PMID:17093501
Abstract

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.

摘要

干扰素-γ和白细胞介素-4(IL-4)分别通过差异激活信号转导子和转录激活子(STAT)1和STAT6,在巨噬细胞中诱导不同的基因表达谱。细胞因子信号转导抑制因子(SOCS)-1作为干扰素-γ信号的负调节因子的作用已得到充分证实。然而,其作为IL-4信号负调节因子的潜在作用尚未被探索。我们发现,与干扰素-γ一样,IL-4在原代巨噬细胞中诱导SOCS-1的快速从头表达。IL-4诱导SOCS-1基因表达依赖于STAT6,而干扰素-γ诱导SOCS-1则依赖于STAT1。与它们诱导SOCS-1表达的共同能力不同,IL-4还诱导巨噬细胞中SOCS-2的表达,但不诱导SOCS-3的表达,而干扰素-γ诱导SOCS-3的表达,但不诱导SOCS-2的表达。强制表达SOCS-1或SOCS-3,而不是SOCS-2,可抑制IL-4对STAT6的激活。此外,SOCS-1似乎作为巨噬细胞中IL-4信号的内源性调节因子,因为在SOCS-1缺陷(SOCS-1(-/-))巨噬细胞中,STAT6激活的幅度和持续时间以及IL-4介导的基因表达比野生型巨噬细胞中要大得多。我们的研究结果表明,与干扰素-γ一样,IL-4也在巨噬细胞中诱导SOCS-1的表达,并且SOCS-1反馈抑制STAT6反应性基因的表达。

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