| Literature DB >> 30266770 |
Yue Li1, Weiren Liu1, Xiaqun Guan1, Jamie Truscott2, John W Creemers3, Hung-Lin Chen1, Marko Pesu4,5, Rami G El Abiad1, Bahri Karacay2, Joseph F Urban6, David E Elliott1, Mark H Kaplan7, Bruce R Blazar8, M Nedim Ince9,10.
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.Entities:
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Year: 2018 PMID: 30266770 PMCID: PMC6200631 DOI: 10.4049/jimmunol.1700808
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422