Trim33 mediates the proinflammatory function of Th17 cells

Transforming growth factor-β (TGF-β) regulates reciprocal regulatory T cell (T reg) and T helper 17 (Th17) differentiation, the underlying mechanism of which is still not understood. Here, we report that tripartite motif-containing 33 (Trim33), a modulator of TGF-β signaling that associates with Sma...

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Veröffentlicht in:The Journal of experimental medicine 2018-07, Vol.215 (7), p.1853-1868
Hauptverfasser: Tanaka, Shinya, Jiang, Yu, Martinez, Gustavo J, Tanaka, Kentaro, Yan, Xiaowei, Kurosaki, Tomohiro, Kaartinen, Vesa, Feng, Xin-Hua, Tian, Qiang, Wang, Xiaohu, Dong, Chen
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Sprache:eng
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Zusammenfassung:Transforming growth factor-β (TGF-β) regulates reciprocal regulatory T cell (T reg) and T helper 17 (Th17) differentiation, the underlying mechanism of which is still not understood. Here, we report that tripartite motif-containing 33 (Trim33), a modulator of TGF-β signaling that associates with Smad2, regulates the proinflammatory function of Th17 cells. Trim33 deficiency in T cells ameliorated an autoimmune disease in vivo Trim33 was required for induction in vitro of Th17, but not T reg cells. Moreover, Smad4 and Trim33 play contrasting roles in the regulation of IL-10 expression; loss of Trim33 enhanced IL-10 production. Furthermore, Trim33 was recruited to the and gene loci, dependent on Smad2, and mediated their chromatin remodeling during Th17 differentiation. Trim33 thus promotes the proinflammatory function of Th17 cells by inducing IL-17 and suppressing IL-10 expression.
ISSN:0022-1007
1540-9538
DOI:10.1084/jem.20170779