Original Article

The Journal of the Korean Rheumatism Association 2009; 16(2): 123-132

Published online June 30, 2009

© Korean College of Rheumatology

류마티스관절염 활막세포에서 TLR3 자극에 따른 MIF 생성의 증가

허양미1ㆍ박성환2ㆍ박미경1ㆍ오혜좌1ㆍ강귀영2ㆍ조미라1

가톨릭대학교 의과학연구원 류마티스 연구센터1, 가톨릭대학교 의과대학 류마티스내과학교실2

Upregulation of Macrophage Migration Inhibitory Factor (MIF) Production by Engagement of Toll-like Receptor 3 (TLR3) on Fibroblast-like Synoviocyte (FLS) from Patients with Rheumatoid Arthritis

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

Abstract

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

Article

Original Article

The Journal of the Korean Rheumatism Association 2009; 16(2): 123-132

Published online June 30, 2009

Copyright © Korean College of Rheumatology.

류마티스관절염 활막세포에서 TLR3 자극에 따른 MIF 생성의 증가

허양미1ㆍ박성환2ㆍ박미경1ㆍ오혜좌1ㆍ강귀영2ㆍ조미라1

가톨릭대학교 의과학연구원 류마티스 연구센터1, 가톨릭대학교 의과대학 류마티스내과학교실2

Upregulation of Macrophage Migration Inhibitory Factor (MIF) Production by Engagement of Toll-like Receptor 3 (TLR3) on Fibroblast-like Synoviocyte (FLS) from Patients with Rheumatoid Arthritis

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

Abstract

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

JRD
Jan 01, 2025 Vol.32 No.1, pp. 1~7
COVER PICTURE
Cumulative growth of rheumatology members and specialists (1980~2024). Cumulative distribution of the number of the (A) Korean College of Rheumatology members and (B) rheumatology specialists. (J Rheum Dis 2025;32:63-65)

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