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白细胞介素-4通过依赖和不依赖信号转导子和转录激活子6的机制抑制肿瘤坏死因子-α和白细胞介素-12的产生。

IL-4 inhibits the production of TNF-alpha and IL-12 by STAT6-dependent and -independent mechanisms.

作者信息

Levings M K, Schrader J W

机构信息

The Biomedical Research Centre, University of British Columbia, Vancouver, Canada.

出版信息

J Immunol. 1999 May 1;162(9):5224-9.

Abstract

IL-4 promotes allergic responses and inhibits the production of proinflammatory cytokines by monocytes and macrophages. The promotion of allergic responses by IL-4 has been shown to be absolutely dependent on the transcription factor STAT6. We report here that the inhibitory effects of IL-4 on the production of TNF-alpha or IL-12 by macrophages had both STAT6-dependent and -independent components, depending on the stimuli. IL-4 failed to inhibit the release of TNF-alpha or IL-12 from STAT6 null macrophages stimulated with LPS alone. However, IL-4 still induced significant inhibition of the production of TNF-alpha and IL-12 from STAT6 null macrophages that were stimulated with the more physiologically relevant combination of LPS and IFN-gamma. These data show that STAT6 is required for the IL-4-mediated inhibition of the production of TNF-alpha and IL-12 stimulated by LPS alone, but that IL-4 also activates distinct, STAT6 independent mechanism(s) that inhibit the IFN-gamma-mediated enhancement of IL-12 and TNF-alpha production.

摘要

白细胞介素-4促进过敏反应,并抑制单核细胞和巨噬细胞产生促炎细胞因子。白细胞介素-4对过敏反应的促进作用已被证明完全依赖于转录因子信号转导子和转录激活子6(STAT6)。我们在此报告,白细胞介素-4对巨噬细胞产生肿瘤坏死因子-α(TNF-α)或白细胞介素-12(IL-12)的抑制作用具有依赖于STAT6和不依赖于STAT6的成分,这取决于刺激因素。白细胞介素-4不能抑制单独用脂多糖(LPS)刺激的STAT6缺陷巨噬细胞释放TNF-α或IL-12。然而,白细胞介素-4仍然能显著抑制用更符合生理情况的LPS和γ干扰素(IFN-γ)组合刺激的STAT6缺陷巨噬细胞产生TNF-α和IL-12。这些数据表明,STAT6是白细胞介素-4介导的抑制单独由LPS刺激产生TNF-α和IL-12所必需的,但白细胞介素-4也激活了不同的、不依赖于STAT6的机制,这些机制抑制IFN-γ介导的IL-12和TNF-α产生的增强。

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