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Publication : Developmentally regulated GTP-binding protein 2 ameliorates EAE by suppressing the development of TH17 cells.

First Author  Ko MS Year  2014
Journal  Clin Immunol Volume  150
Issue  2 Pages  225-35
PubMed ID  24463315 Mgi Jnum  J:209442
Mgi Id  MGI:5567868 Doi  10.1016/j.clim.2013.12.004
Citation  Ko MS, et al. (2014) Developmentally regulated GTP-binding protein 2 ameliorates EAE by suppressing the development of TH17 cells. Clin Immunol 150(2):225-35
abstractText  Developmentally regulated GTP-binding protein 2 (DRG2) represents a novel subclass of GTP-binding proteins. We here report that transgenic overexpression of DRG2 in mice ameliorates experimental autoimmune encephalomyelitis (EAE), a murine model of multiple sclerosis (MS). The protective effect of DRG2 in EAE was mediated by the inhibition of the development of T(H)17 cells. DRG2 enhanced the activity of PPARgamma, which led to an inhibition of the nuclear factor kappa B (NF-kappaB) activity and IL-6 production in antigen presenting cells and an inhibition of the development of T(H)17 cells. Our results demonstrate that DRG2 is an essential modulator of EAE.
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