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Correlations between both the expression levels of inflammatory mediators and growth factor in medial perimeniscal synovial tissue and the severity of medial knee osteoarthritis
Authors:Liang Ning  Muneaki Ishijima  Haruka Kaneko  Hidetake Kurihara  Eri Arikawa-Hirasawa  Mitsuaki Kubota  Lizu Liu  Zhuo Xu  Ippei Futami  Anwarjan Yusup  Katsumi Miyahara  Shouyu Xu  Kazuo Kaneko  Hisashi Kurosawa
Affiliation:1. Department of Medicine for Motor Organ, Juntendo University Graduate School of Medicine, Tokyo, Japan
2. Department of Orthopaedics, Juntendo University School of Medicine, 2-1-1, Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan
3. Sportology Center, Juntendo University Graduate School of Medicine, Tokyo, Japan
4. Department of Anatomy and Life Structure, Juntendo University Graduate School of Medicine, Tokyo, Japan
5. Research Institute for Diseases of Old Ages, Juntendo University Graduate School of Medicine, Tokyo, Japan
6. Division of Biomedical Imaging Research, Biomedical Research Center, Juntendo University Graduate School of Medicine, Tokyo, Japan
Abstract:An enhanced expression of the inflammatory mediators in the perimeniscal synovium in knee osteoarthritis (OA) has been suggested to contribute to progressive cartilage degeneration. However, whether the expression levels of these molecules correlated with the severity of OA still remained unclear. Medial perimeniscal synovial samples were obtained from 23 patients with Kellgren-Lawrence (K/L) grades 2 to 4 of medial knee OA. Immunohistochemical analysis of the synovium revealed that the MMP-1, COX-2 and IL-1β expression of the patients with K/L 4 to be significantly reduced in comparison to those with either K/L 2 or 3, while the TGF-β expression showed the opposite. The synovial expression of MMP-1 and IL-1β showed a significant negative correlation with the severity of OA, while that of TGF-β again showed the opposite. In conclusion, although synovial inflammation remained active, the MMP-1, COX-2 and IL-1β expression in synovium decreased depending upon the severity of OA, while the TGF-β expression increased.
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