Cited by 187Cytokine Signaling Pathways and InteractionsNF-κB Signaling PathwaysT-cell and B-cell Immunology

Cutting Edge: A Transcriptional Repressor and Corepressor Induced by the STAT3-Regulated Anti-Inflammatory Signaling Pathway

El Kasmi, Karim C, Smith, Amber M, Williams, Lynn, Neale, Geoffrey, Panopolous, Athanasia, Watowich, Stephanie S, Häcker, Hans, Foxwell, Brian M J +1 more·2007·The Journal of Immunology

Abstract

IL-10 regulates anti-inflammatory signaling via the activation of STAT3, which in turn controls the induction of a gene expression program whose products execute inhibitory effects on proinflammatory mediator production. In this study we show that IL-10 induces the expression of an ETS family transcriptional repressor, ETV3, and a helicase family corepressor, Strawberry notch homologue 2 (SBNO2), in mouse and human macrophages. IL-10-mediated induction of ETV3 and SBNO2 expression was dependent upon both STAT3 and a stimulus through the TLR pathway. We also observed that ETV3 expression was strongly induced by the STAT3 pathway regulated by IL-10 but not by STAT3 signaling activated by IL-6, which cannot activate the anti-inflammatory signaling pathway. ETV3 and SBNO2 repressed NF-kappaB- but not IFN regulatory factor 7 (IRF7)-activated transcriptional reporters. Collectively our data suggest that ETV3 and SBNO2 are components of the pathways that contribute to the downstream anti-inflammatory effects of IL-10.

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Crossref · 10.4049/jimmunol.179.11.7215

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Authors
El Kasmi, K. C., Smith, A. M., Williams, L., Neale, G., Panopolous, A., Watowich, S. S., Häcker, H., Foxwell, B. M. J., & Murray, P. J.
Affiliations
  • Department of Infectious Diseases, St. Jude Children’s Research Hospital , Memphis, TN 38105
  • St. Jude Children's Research Hospital (US)
  • Imperial College London (GB)
  • The University of Texas MD Anderson Cancer Center (US)
Venue
The Journal of Immunology
Published
2007-12-01
Volume
179
Issue
11
Pages
7215-7219
ISSN
  • 0022-1767 (ISSN-L)
  • 1550-6606
OpenAlex
W2127303484
Cited by
182
References
30
Citations by year
2026: 5 · 2025: 10 · 2024: 13 · 2023: 15 · 2022: 9 · 2021: 15 · 2020: 8 · 2019: 8 · 2018: 8 · 2017: 5 · 2016: 8 · 2015: 10 · 2014: 6 · 2013: 11 · 2012: 14
FWCI
4.89
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Immunology (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Cancer Institute (T32CA009598, P 30CA 21765, P30CA021765, T32 CA09598-16)
Topics
  • Health Sciences › Medicine › Oncology › Cytokine Signaling Pathways and Interactions
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
Keywords
IL-10, STAT3 signaling, transcriptional repressor, corepressors, anti-inflammatory signaling, macrophages, NF-κB, IRF7, interleukin-6
MeSH terms
Animals, Anti-Inflammatory Agents, Non-Steroidal, Cell Line, Gene Expression Regulation, Humans, Macrophages, Mice, Inbred C57BL, Repressor Proteins, RNA, Messenger, Time Factors, Transcription Factors, Signal Transduction, Interleukin-10, Mice, Knockout, RNA, Small Interfering, Proto-Oncogene Proteins c-ets, STAT3 Transcription Factor, Mice

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