TY - JOUR
T1 - Cutting edge
T2 - A transcriptional repressor and corepressor induced by the STAT3-regulated anti-inflammatory signaling pathway
AU - El Kasmi, Karim C.
AU - Smith, Amber M.
AU - Williams, Lynn
AU - Neale, Geoffrey
AU - Panopolous, Athanasia
AU - Watowich, Stephanie S.
AU - Häcker, Hans
AU - Foxwell, Brian M.J.
AU - Murray, Peter J.
PY - 2007/12/1
Y1 - 2007/12/1
N2 - 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-κB- 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.
AB - 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-κB- 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.
UR - http://www.scopus.com/inward/record.url?scp=38849147783&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=38849147783&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.179.11.7215
DO - 10.4049/jimmunol.179.11.7215
M3 - Article
C2 - 18025162
AN - SCOPUS:38849147783
SN - 0022-1767
VL - 179
SP - 7215
EP - 7219
JO - Journal of Immunology
JF - Journal of Immunology
IS - 11
ER -