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논문 기본 정보

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학술저널
저자정보
Kim, Dong Hyeok (Division of Applied Life Science, Gyeongsang National University) Ihn, Hyun-Ju (Division of Applied Life Science, Gyeongsang National University) Moon, Chaerin (Division of Applied Life Science, Gyeongsang National University) Oh, Sang-Seok (Division of Applied Life Science, Gyeongsang National University) Park, Soojong (Division of Applied Life Science, Gyeongsang National University) Kim, Suk (College of Veterinary Medicine, Gyeongsang National University) Lee, Keun Woo (Division of Applied Life Science, Gyeongsang National University) Kim, Kwang Dong (Division of Applied Life Science, Gyeongsang National University)
저널정보
한국응용약물학회 Biomolecules & Therapeutics(구 응용약물학회지) Biomolecules & therapeutics 제23권 제1호
발행연도
2015.1
수록면
71 - 76 (6page)

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Peroxisome proliferator-activated receptor gamma ($PPAR{\gamma}$) was identified as a cell-intrinsic regulator of Th17 cell differentiation. Th17 cells have been associated with several autoimmune diseases, including experimental autoimmune encephalomyelitis (EAE), inflammatory bowel disease (IBD), and collagen-induced arthritis. In this study, we confirmed $PPAR{\gamma}$-mediated inhibition of Th17 cell differentiation and cytokine production at an early stage. Treatment with ciglitazone, a $PPAR{\gamma}$ ligand, reduced both IL-$1{\beta}$-mediated enhancement of Th17 differentiation and activation of Th17 cells after polarization. For Th17 cell differentiation, we found that ciglitazone-treated cells had a relatively low proliferative activity and produced a lower amount of cytokines, regardless of the presence of IL-$1{\beta}$. The inhibitory activity of ciglitazone might be due to decrease of CCNB1 expression, which regulates the cell cycle in T cells. Hence, we postulate that a pharmaceutical $PPAR{\gamma}$ activator might be a potent candidate for treatment of Th17-mediated autoimmune disease patients.

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