c-Maf Regulates IL-10 Expression during Th17 Polarization

Jiangnan Xu(Cell and Gene Therapy Catapult), Yu Yang(Mount Sinai Hospital), Guixing Qiu(Chinese Academy of Medical Sciences & Peking Union Medical College), Girdhari Lal(Cell and Gene Therapy Catapult), Zhihong Wu(Chinese Academy of Medical Sciences & Peking Union Medical College), David E. Levy(New York University), Jordi Ochando(Instituto de Salud Carlos III), Jonathan S. Bromberg(Mount Sinai Hospital), Yaozhong Ding(Mount Sinai Hospital)
The Journal of Immunology
May 1, 2009
Cited by 228Open Access
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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.


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