TY - JOUR
T1 - Mechanism of Interferon-gamma mediated down-regulation of Interleukin-10 gene expression
AU - Schaefer, Annette
AU - Unterberger, Claudia
AU - Frankenberger, Marion
AU - Lohrum, Marion
AU - Staples, Karl J.
AU - Werner, Thomas
AU - Stunnenberg, Henk
AU - Ziegler-Heitbrock, Loems
N1 - Funding Information:
This work was supported by grants from MediSearch, Leicester, UK, from DFG, Bonn, Germany (FR154) and BBSRC, UK (91-C19230). We thank Dr. Wieland Wolf Rentschler Biotechnologie, Laupheim, Germany for generous provision of INFγ and Dr. Sabine Ehrt and Carl Nathan, Weill Medical College of Cornell University, New York, USA, for providing the detailed information on IFNγ-regulated genes in mouse macrophages.
PY - 2009/4
Y1 - 2009/4
N2 - 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.
AB - 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.
KW - Interferon-gamma
KW - Interleukin-10
KW - Stat3
UR - http://www.scopus.com/inward/record.url?scp=62549083836&partnerID=8YFLogxK
U2 - 10.1016/j.molimm.2008.11.015
DO - 10.1016/j.molimm.2008.11.015
M3 - Article
C2 - 19124156
AN - SCOPUS:62549083836
SN - 0161-5890
VL - 46
SP - 1351
EP - 1359
JO - Molecular Immunology
JF - Molecular Immunology
IS - 7
ER -