Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/4588
Title: Mechanism of Interferon-gamma mediated down-regulation of Interleukin-10 gene expression
Authors: Schaefer, Annette
Unterberger, Claudia
Frankenberger, Marion
Lohrum, Marion
Staples, Karl J.
Werner, Thomas
Stunnenberg, Henk
Ziegler-Heitbrock, Loems
First Published: Apr-2009
Publisher: Elsevier
Citation: Molecular Immunology, 2009, 46 (7), pp. 1351-1359.
Abstract: 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.
DOI Link: 10.1016/j.molimm.2008.11.015
ISSN: 0161-5890
Links: http://www.sciencedirect.com/science/article/pii/S0161589008007724
http://hdl.handle.net/2381/4588
Type: Article
Rights: This is the author's final draft of the paper published as Molecular Immunology, 2009, 46 (7), pp. 1351-1359. The final version is available from http://www.sciencedirect.com. Doi: 10.1016/j.molimm.2008.11.015
Appears in Collections:Published Articles, Dept. of Infection, Immunity and Inflammation

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