STAT6
肿瘤坏死因子α
白细胞介素4
促炎细胞因子
免疫学
细胞因子
化学
细胞生物学
生物
炎症
作者
Megan K. Levings,John W. Schrader
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:1999-05-01
卷期号:162 (9): 5224-5229
被引量:96
标识
DOI:10.4049/jimmunol.162.9.5224
摘要
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-α 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-α or IL-12 from STAT6 null macrophages stimulated with LPS alone. However, IL-4 still induced significant inhibition of the production of TNF-α and IL-12 from STAT6 null macrophages that were stimulated with the more physiologically relevant combination of LPS and IFN-γ. These data show that STAT6 is required for the IL-4-mediated inhibition of the production of TNF-α and IL-12 stimulated by LPS alone, but that IL-4 also activates distinct, STAT6 independent mechanism(s) that inhibit the IFN-γ-mediated enhancement of IL-12 and TNF-α production.
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