Trim33 mediates the proinflammatory function of Th17 cells

J Exp Med. 2018 Jul 2;215(7):1853-1868. doi: 10.1084/jem.20170779. Epub 2018 Jun 21.

Abstract

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 Il17a and Il10 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Chromatin / metabolism
  • Genetic Loci
  • Genome
  • Histones / metabolism
  • Humans
  • Inflammation / immunology*
  • Inflammation / pathology*
  • Interleukin-10 / metabolism
  • Interleukin-17 / metabolism
  • Mice, Inbred C57BL
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / metabolism
  • Protein Processing, Post-Translational
  • Smad2 Protein / metabolism
  • Smad4 Protein / metabolism
  • T-Lymphocytes, Regulatory / immunology
  • Th17 Cells / immunology*
  • Transcription Factors / deficiency
  • Transcription Factors / metabolism*
  • Up-Regulation

Substances

  • Chromatin
  • Histones
  • Interleukin-17
  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • Smad2 Protein
  • Smad4 Protein
  • Transcription Factors
  • Trim33 protein, mouse
  • Interleukin-10