The Journal of the Korean Rheumatism Association 2009; 16(2): 123-132
Published online June 30, 2009
© Korean College of Rheumatology
허양미1ㆍ박성환2ㆍ박미경1ㆍ오혜좌1ㆍ강귀영2ㆍ조미라1
가톨릭대학교 의과학연구원 류마티스 연구센터1, 가톨릭대학교 의과대학 류마티스내과학교실2
Correspondence to : Sung-Hwan Park
Objective: Rheumatoid arthritis (RA) is a chronic autoimmune disease. Macrophage migration inhibitory factor (MIF) has been shown to be an important pro-inflammatory cytokine in RA. The aim of this study was to determine if the engagement of toll-like receptor 3 (TLR3) induces the production of MIF in the fibroblast-like synoviocytes (FLS) of patients with RA. Methods: The expression of inflammatory cytokines (e.g. MIF, IL-6, IL-1Ղ and TNFՁ) and toll-like receptors (e.g. TLR2, TLR3 and TLR4) in the synovial tissue were quantified by immunohistochemistry. FLS were isolated from the synovial tissues of patients with RA and stimulated with TLR-3 ligand polyI:C, in the presence of a neutralizing antibody against IL-6. The concentrations of MIF and IL-6 in the culture supernatants from the FLS were measured using sandwich ELISA. Results: The engagement of TLR3 with PolyI:C increased the production of MIF in FLS. The stimulatory effect of these TLR ligands showed a dose-dependent trend. The combination of TLR3 and TLR4 synergistically increased the level of MIF and IL-6 production. The addition of neutralizing antibodies against IL-6 abrogated the stimulatory effect of the ligands of TLR3 and TLR4 on the production of MIF. Conclusion: These results show that TLR3 engagement stimulates the production of MIF and IL-6. Therefore, the TLRs help perpetuate of RA pathogenesis through production of MIF from the FLS in patients with RA, and might provide a new therapeutic approach for the treatment of rheumatoid arthritis.
Keywords Rheumatoid arthritis, Fibroblast-like synoviocytes, Macrophage migration inhibitory factor, Toll-like receptor engagement
The Journal of the Korean Rheumatism Association 2009; 16(2): 123-132
Published online June 30, 2009
Copyright © Korean College of Rheumatology.
허양미1ㆍ박성환2ㆍ박미경1ㆍ오혜좌1ㆍ강귀영2ㆍ조미라1
가톨릭대학교 의과학연구원 류마티스 연구센터1, 가톨릭대학교 의과대학 류마티스내과학교실2
Yang Mi Her1, Sung-Hwan Park2, Mi Kyung Park1, Hye-Jwa Oh1, Kwi Young Kang2, Mi-La Cho1
The Rheumatism Resarch Center, Catholic Research Institute of Medical Science1, Division of Rheumatology, Department of Internal Medicine, College of Medicine2, The Catholic University of Korea, Seoul, Korea
Correspondence to:Sung-Hwan Park
Objective: Rheumatoid arthritis (RA) is a chronic autoimmune disease. Macrophage migration inhibitory factor (MIF) has been shown to be an important pro-inflammatory cytokine in RA. The aim of this study was to determine if the engagement of toll-like receptor 3 (TLR3) induces the production of MIF in the fibroblast-like synoviocytes (FLS) of patients with RA. Methods: The expression of inflammatory cytokines (e.g. MIF, IL-6, IL-1Ղ and TNFՁ) and toll-like receptors (e.g. TLR2, TLR3 and TLR4) in the synovial tissue were quantified by immunohistochemistry. FLS were isolated from the synovial tissues of patients with RA and stimulated with TLR-3 ligand polyI:C, in the presence of a neutralizing antibody against IL-6. The concentrations of MIF and IL-6 in the culture supernatants from the FLS were measured using sandwich ELISA. Results: The engagement of TLR3 with PolyI:C increased the production of MIF in FLS. The stimulatory effect of these TLR ligands showed a dose-dependent trend. The combination of TLR3 and TLR4 synergistically increased the level of MIF and IL-6 production. The addition of neutralizing antibodies against IL-6 abrogated the stimulatory effect of the ligands of TLR3 and TLR4 on the production of MIF. Conclusion: These results show that TLR3 engagement stimulates the production of MIF and IL-6. Therefore, the TLRs help perpetuate of RA pathogenesis through production of MIF from the FLS in patients with RA, and might provide a new therapeutic approach for the treatment of rheumatoid arthritis.
Keywords: Rheumatoid arthritis, Fibroblast-like synoviocytes, Macrophage migration inhibitory factor, Toll-like receptor engagement
Young-Eun Park, Sung-Il Kim, Seong-Hu Park, Seung-Hoon Baek, Hye-Jwa Oh, Yang-Mi Heo, Mi-La Cho
The Journal of the Korean Rheumatism Association 2010; 17(3): 238-245Yong-Jin Kwon, Soo-Jin Chung, Tae-Yeon Kim, Min-Chan Park
The Journal of the Korean Rheumatism Association 2010; 17(2): 153-161Ju Kyoung Song, M.D., Hyun Young Shin, M.D., You Sun Lee, M.D., Jae Hee Hwang, M.D., Yang Sook Kwon, M.D.*, Yeon Ju Jeong, M.D.*, Yun Jong Lee, M.D.**, Seong Wook Kang, M.D.
The Journal of the Korean Rheumatism Association 2005; 12(2): 108-115