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

• Published in: Clinical immunology (Orlando, Fla.) Vol. 150; no. 2; pp. 225 - 235
• Main Authors: Ko, Myoung Seok, Kim, Hyo Jeong, Kim, Hong Kyung, Yoon, Nal Ae, Lee, Unn Hwa, Lee, Sang Chul, Chung, Dae Kyun, Lee, Byung Ju, Suh, Jae Hee, Cho, Wha Ja, Park, Jeong Woo
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.02.2014
• Subjects: Animals; Antigen-Presenting Cells - immunology; Antigen-Presenting Cells - metabolism; Cell Differentiation; Co-Repressor Proteins - metabolism; Cytokines - metabolism; DRG2; EAE; Encephalomyelitis, Autoimmune, Experimental - genetics; Encephalomyelitis, Autoimmune, Experimental - immunology; Encephalomyelitis, Autoimmune, Experimental - metabolism; Gene Expression; Genotype; GTP-Binding Proteins - genetics; GTP-Binding Proteins - metabolism; IL-6; Inflammation Mediators - metabolism; Interleukin-6 - genetics; Interleukin-6 - metabolism; Male; Mice; Mice, Transgenic; NF-kappa B - metabolism; NF-κB; PPAR gamma - metabolism; PPARγ; Promoter Regions, Genetic; Protein Binding; T-Lymphocyte Subsets - cytology; T-Lymphocyte Subsets - immunology; T-Lymphocyte Subsets - metabolism; TH17; Th17 Cells - cytology; Th17 Cells - immunology; Th17 Cells - metabolism; EAE; NF-κB; DRG2; TH17; PPARγ; IL-6; T(H)17
• ISSN: 1521-6616; 1521-7035
• DOI: 10.1016/j.clim.2013.12.004

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 TH17 cells. DRG2 enhanced the activity of PPARγ, which led to an inhibition of the nuclear factor kappa B (NF-κB) activity and IL-6 production in antigen presenting cells and an inhibition of the development of TH17 cells. Our results demonstrate that DRG2 is an essential modulator of EAE. •DRG2 interacts with PPARγ in APCs.•DRG2 enhances the sumoylation and the activity of PPARγ.•Activated PPARγ suppresses binding of NF-κB to the IL-6 promoter region.•Reduced IL-6 from APCs results in the TH17 deficiency and amelioration of EAE.