<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xu J</submitter><funding>NIAID NIH HHS</funding><pagination>6226-36</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2834209</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>182(10)</volume><pubmed_abstract>IL-10 production by Th17 cells is critical for limiting autoimmunity and inflammatory responses. Gene array analysis on Stat6 and T-bet double-deficient Th17 cells identified the Th2 transcription factor c-Maf to be synergistically up-regulated by IL-6 plus TGFbeta and associated with Th17 IL-10 production. Both c-Maf and IL-10 induction during Th17 polarization depended on Stat3, but not Stat6 or Stat1, and mechanistically differed from IL-10 regulation by Th2 or IL-27 signals. TGFbeta was also synergistic with IL-27 to induce c-Maf, and it induced Stat1-independent IL-10 expression in contrast to IL-27 alone. Retroviral transduction of c-Maf was able to induce IL-10 expression in Stat6-deficient CD4 and CD8 T cells, and c-Maf directly transactivated IL-10 gene expression through binding to a MARE (Maf recognition element) motif in the IL-10 promoter. Taken together, these data reveal a novel role for c-Maf in regulating T effector development, and they suggest that TGFbeta may antagonize Th17 immunity by IL-10 production through c-Maf induction.</pubmed_abstract><journal>Journal of immunology (Baltimore, Md. : 1950)</journal><pubmed_title>c-Maf regulates IL-10 expression during Th17 polarization.</pubmed_title><pmcid>PMC2834209</pmcid><funding_grant_id>R01 AI062855</funding_grant_id><funding_grant_id>R01 AI 62855</funding_grant_id><funding_grant_id>R01 AI041428</funding_grant_id><funding_grant_id>AI 41428</funding_grant_id><funding_grant_id>R56 AI041428</funding_grant_id><funding_grant_id>R21 AI041428</funding_grant_id><funding_grant_id>R01 AI062855-01A1</funding_grant_id><pubmed_authors>Wu Z</pubmed_authors><pubmed_authors>Qiu G</pubmed_authors><pubmed_authors>Lal G</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Ding Y</pubmed_authors><pubmed_authors>Bromberg JS</pubmed_authors><pubmed_authors>Levy DE</pubmed_authors><pubmed_authors>Ochando JC</pubmed_authors><pubmed_authors>Xu J</pubmed_authors></additional><is_claimable>false</is_claimable><name>c-Maf regulates IL-10 expression during Th17 polarization.</name><description>IL-10 production by Th17 cells is critical for limiting autoimmunity and inflammatory responses. Gene array analysis on Stat6 and T-bet double-deficient Th17 cells identified the Th2 transcription factor c-Maf to be synergistically up-regulated by IL-6 plus TGFbeta and associated with Th17 IL-10 production. Both c-Maf and IL-10 induction during Th17 polarization depended on Stat3, but not Stat6 or Stat1, and mechanistically differed from IL-10 regulation by Th2 or IL-27 signals. TGFbeta was also synergistic with IL-27 to induce c-Maf, and it induced Stat1-independent IL-10 expression in contrast to IL-27 alone. Retroviral transduction of c-Maf was able to induce IL-10 expression in Stat6-deficient CD4 and CD8 T cells, and c-Maf directly transactivated IL-10 gene expression through binding to a MARE (Maf recognition element) motif in the IL-10 promoter. Taken together, these data reveal a novel role for c-Maf in regulating T effector development, and they suggest that TGFbeta may antagonize Th17 immunity by IL-10 production through c-Maf induction.</description><dates><release>2009-01-01T00:00:00Z</release><publication>2009 May</publication><modification>2020-11-19T12:49:45Z</modification><creation>2019-06-06T21:55:36Z</creation></dates><accession>S-EPMC2834209</accession><cross_references><pubmed>19414776</pubmed><doi>10.4049/jimmunol.0900123</doi></cross_references></HashMap>