| Literature DB >> 28356385 |
Violeta Rus1,2, Vinh Nguyen3,2, Alexandru Tatomir2,4, Jason R Lees5, Armugam P Mekala2,4, Dallas Boodhoo2,4, Cosmin A Tegla2,4, Irina G Luzina3,2, Paul A Antony6, Cornelia D Cudrici7, Tudor C Badea8, Horea G Rus2,4.
Abstract
Th17 cells play a critical role in autoimmune diseases, including multiple sclerosis and its animal model, experimental autoimmune encephalomyelitis. Response gene to complement (RGC)-32 is a cell cycle regulator and a downstream target of TGF-β that mediates its profibrotic activity. In this study, we report that RGC-32 is preferentially upregulated during Th17 cell differentiation. RGC-32-/- mice have normal Th1, Th2, and regulatory T cell differentiation but show defective Th17 differentiation in vitro. The impaired Th17 differentiation is associated with defects in IFN regulatory factor 4, B cell-activating transcription factor, retinoic acid-related orphan receptor γt, and SMAD2 activation. In vivo, RGC-32-/- mice display an attenuated experimental autoimmune encephalomyelitis phenotype accompanied by decreased CNS inflammation and reduced frequency of IL-17- and GM-CSF-producing CD4+ T cells. Collectively, our results identify RGC-32 as a novel regulator of Th17 cell differentiation in vitro and in vivo and suggest that RGC-32 is a potential therapeutic target in multiple sclerosis and other Th17-mediated autoimmune diseases.Entities:
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Year: 2017 PMID: 28356385 PMCID: PMC6197070 DOI: 10.4049/jimmunol.1602158
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422