1. Academic Validation
  2. Cutting edge: A transcriptional repressor and corepressor induced by the STAT3-regulated anti-inflammatory signaling pathway

Cutting edge: A transcriptional repressor and corepressor induced by the STAT3-regulated anti-inflammatory signaling pathway

  • J Immunol. 2007 Dec 1;179(11):7215-9. doi: 10.4049/jimmunol.179.11.7215.
Karim C El Kasmi 1 Amber M Smith Lynn Williams Geoffrey Neale Athanasia D Panopoulos Stephanie S Watowich Hans Häcker Brian M J Foxwell Peter J Murray
Affiliations

Affiliation

  • 1 Department of Infectious Diseases, St Jude Children's Research Hospital, Memphis, TN 38105, USA.
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.

Figures