The Journal of the Korean Rheumatism Association 2005; 12(2): 73-82
Published online June 30, 2005
© Korean College of Rheumatology
강영모·김성일*·김정섭*·유동완·사금희·박은주·김성욱·서재석·한승우·남언정·경희수**·김문규***·김인산†·김정철***
경북대학교 의과대학 내과학교실, 부산대학교 의과대학 내과학교실*, 경북대학교 의과대학 정형외과학교실**, 면역학교실***, 생화학교실†
Objective: To investigate the expression pattern of transforming growth factor-β-inducible gene-h3 (βig-h3) within rheumatoid synovial tissue and the regulation of βig-h3 synthesis in fibroblast-like synoviocyte (FLS). Methods: Synovial tissues obtained from patients with rheumatoid arthritis and osteoarthritis were obtained during joint replacement surgery. βig-h3 expression was evaluated with immunohistochemical stain. FLS was isolated from synovial tissues and stimulated with cytokines including TGF-β, TNF-α, IL-1β, IFN-γ, IL-6, IL-4, and IL-10. βig-h3 synthesis was measured using semiquantitative RT-PCR, ELISA, immunofluorescence stain, and flow cytometry. Results: Expression of βig-h3 was diffuse and abundant in both lining and sublining layers of rheumatoid synovium, which was more prominent than those of osteoarthritis. Production of βig-h3 in FLS was regulated by TGF-β1 in a dose-dependent manner and was highest at 5 ng/mL of TGF-β1. TNF-α and IL-1β upregulated the production of βig-h3 from FLS synergistically with TGF-β1 but other cytokines such as IL-4, IL-6, IL-10 did not affect. βig-h3 synthesis was efficiently inhibited by dexamethasone at higher dose (100 nM) but not by cyclosporine-A. Conclusion: Production of βig-h3, which is highly upregulated in rheumatoid synovitis, is differentially regulated by inflammatory cytokines.
Keywords Rheumatoid arthritis, Transforming growth factor-β-inducible gene-h3, Fibroblast-like synoviocyte
The Journal of the Korean Rheumatism Association 2005; 12(2): 73-82
Published online June 30, 2005
Copyright © Korean College of Rheumatology.
강영모·김성일*·김정섭*·유동완·사금희·박은주·김성욱·서재석·한승우·남언정·경희수**·김문규***·김인산†·김정철***
경북대학교 의과대학 내과학교실, 부산대학교 의과대학 내과학교실*, 경북대학교 의과대학 정형외과학교실**, 면역학교실***, 생화학교실†
Young Mo Kang, M.D., Sung Il Kim, M.D.*, Jeong Seup Kim, M.S.*, Dong Wan You, Kheum Hee Sa, M.S., Eun Ju Park, B.S., Sung Uk Kim, M.D., Jae Seok Seo, M.D., Seung Woo Han, M.D., Eon Jeong Nam, M.D., Hee-Soo Kyung, M.D.**, Moon Gyu Kim, M.D.***, In San Kim, M.D.†, Jung Chol Kim, M.D.***
Department of Internal Medicine, Kyungpook National University School of Medicine, Daegu, Department of Internal Medicine, Pusan National University School of Medicine*, Busan, Departments of Orthopedic Surgery**, Immunology***, Biochemistry†, Kyungpook National University School of Medicine, Daegu, Korea
Objective: To investigate the expression pattern of transforming growth factor-β-inducible gene-h3 (βig-h3) within rheumatoid synovial tissue and the regulation of βig-h3 synthesis in fibroblast-like synoviocyte (FLS). Methods: Synovial tissues obtained from patients with rheumatoid arthritis and osteoarthritis were obtained during joint replacement surgery. βig-h3 expression was evaluated with immunohistochemical stain. FLS was isolated from synovial tissues and stimulated with cytokines including TGF-β, TNF-α, IL-1β, IFN-γ, IL-6, IL-4, and IL-10. βig-h3 synthesis was measured using semiquantitative RT-PCR, ELISA, immunofluorescence stain, and flow cytometry. Results: Expression of βig-h3 was diffuse and abundant in both lining and sublining layers of rheumatoid synovium, which was more prominent than those of osteoarthritis. Production of βig-h3 in FLS was regulated by TGF-β1 in a dose-dependent manner and was highest at 5 ng/mL of TGF-β1. TNF-α and IL-1β upregulated the production of βig-h3 from FLS synergistically with TGF-β1 but other cytokines such as IL-4, IL-6, IL-10 did not affect. βig-h3 synthesis was efficiently inhibited by dexamethasone at higher dose (100 nM) but not by cyclosporine-A. Conclusion: Production of βig-h3, which is highly upregulated in rheumatoid synovitis, is differentially regulated by inflammatory cytokines.
Keywords: Rheumatoid arthritis, Transforming growth factor-β-inducible gene-h3, Fibroblast-like synoviocyte
Eon Jeong Nam, Eun Joo Song, Ji Min Kim, Jae Seok Seo, Keum Hee Sa, Hyung Jung Cho, Jae Yong Park, Hee-Soo Kyung, In San Kim, Young Mo Kang
The Journal of the Korean Rheumatism Association 2008; 15(3): 222-229Roshan Subedi, M.D., Afrah Misbah, M.D., Adnan Al Najada, M.D., Anthony James Ocon, M.D., Ph.D.
J Rheum Dis -0001; ():Hee Jun Kim, R.N., Ph.D., Ju-Yang Jung, M.D., Ph.D., Ji-Won Kim, M.D., Chang-Hee Suh, M.D., Ph.D., Hyoun-Ah Kim, M.D., Ph.D.
J Rheum Dis -0001; ():