STAT1
荧光素酶
分子生物学
发起人
车站3
报告基因
染色质免疫沉淀
转录因子
化学
干扰素γ
干扰素
转染
基因表达
细胞因子
生物
信号转导
基因
细胞生物学
免疫学
生物化学
作者
Annette E. Schaefer,Claudia Unterberger,Marion Frankenberger,Marion Lohrum,Karl J. Staples,Thomas Werner,Henk Stunnenberg,Loems Ziegler-Heitbrock
标识
DOI:10.1016/j.molimm.2008.11.015
摘要
Expression of the anti-inflammatory cytokine IL-10 is suppressed by the pro-inflammatory interferonγ but the mechanism of this action is unknown. We analysed activity of IL-10 promoter luciferase reporter constructs in transfected RPMI 8226.1 B cells that were treated at −2 h with IFNγ (1000 U/ml) followed by stimulation with LPS (100 ng/ml) at 0 h. IFNγ treatment suppressed LPS-induced IL-10 promoter activity in a construct carrying the −1044 promoter and also one containing the −195 promoter. The suppression was independent of the IRF-motif at −182 but involved the Stat-motif at −120. In gelshift analysis this Stat motif did bind LPS-induced Stat3 and with IFNγ treatment it did, in addition, bind Stat1. ChIP analysis for detection of transcription factor binding to chromatin in intact cells demonstrated Stat3 binding to the proximal IL-10 promoter when cells are stimulated with LPS only. Treatment with IFNγ only led to Stat1 binding in ChIP analysis and treatment with IFNγ plus LPS led to reduced Stat3 binding while Stat1 binding remained high. Finally, LPS-induced activity of the trimeric Stat-motif in front of the luciferase reporter was suppressed by IFNγ. These data demonstrate that IFNγ down-regulates expression of the IL-10 gene by a novel mechanism that involves displacement of transactiving Stat3 by IFNγ-induced Stat1.
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