STAT6 and Furin Are Successive Triggers for the Production of TGF-β by T Cells

J Immunol. 2018 Nov 1;201(9):2612-2623. doi: 10.4049/jimmunol.1700808. Epub 2018 Sep 28.

Abstract

Production of TGF-β by T cells is key to various aspects of immune homeostasis, with defects in this process causing or aggravating immune-mediated disorders. The molecular mechanisms that lead to TGF-β generation by T cells remain largely unknown. To address this issue, we take advantage of the fact that intestinal helminths stimulate Th2 cells besides triggering TGF-β generation by T lymphocytes and regulate immune-mediated disorders. We show that the Th2 cell-inducing transcription factor STAT6 is necessary and sufficient for the expression of TGF-β propeptide in T cells. STAT6 is also necessary for several helminth-triggered events in mice, such as TGF-β-dependent suppression of alloreactive inflammation in graft-versus-host disease. Besides STAT6, helminth-induced secretion of active TGF-β requires cleavage of propeptide by the endopeptidase furin. Thus, for the immune regulatory pathway necessary for TGF-β production by T cells, our results support a two-step model, composed of STAT6 and furin.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Furin / immunology*
  • Furin / metabolism
  • Graft vs Host Disease / immunology
  • Mice
  • STAT6 Transcription Factor / immunology*
  • STAT6 Transcription Factor / metabolism
  • Strongylida Infections / immunology
  • T-Lymphocytes / immunology*
  • Transforming Growth Factor beta / biosynthesis*

Substances

  • STAT6 Transcription Factor
  • Stat6 protein, mouse
  • Transforming Growth Factor beta
  • Furin