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J Immunol ; 201(9): 2612-2623, 2018 11 01.
Article in English | MEDLINE | ID: mdl-30266770

ABSTRACT

Production of TGF-ß 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-ß 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-ß 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-ß propeptide in T cells. STAT6 is also necessary for several helminth-triggered events in mice, such as TGF-ß-dependent suppression of alloreactive inflammation in graft-versus-host disease. Besides STAT6, helminth-induced secretion of active TGF-ß requires cleavage of propeptide by the endopeptidase furin. Thus, for the immune regulatory pathway necessary for TGF-ß production by T cells, our results support a two-step model, composed of STAT6 and furin.


Subject(s)
Furin/immunology , STAT6 Transcription Factor/immunology , T-Lymphocytes/immunology , Transforming Growth Factor beta/biosynthesis , Animals , Furin/metabolism , Graft vs Host Disease/immunology , Mice , STAT6 Transcription Factor/metabolism , Strongylida Infections/immunology
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