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Monocarboxylate Transporter 4, Associated With the Acidification of Synovial Fluid, Is a Novel Therapeutic Target for Inflammatory Arthritis
Author(s) -
Fujii Wataru,
Kawahito Yutaka,
Nagahara Hidetake,
Kukida Yuji,
Seno Takahiro,
Yamamoto Aihiro,
Kohno Masataka,
Oda Ryo,
Taniguchi Daigo,
Fujiwara Hiroyoshi,
Ejima Akika,
Kishida Tsunao,
Mazda Osam,
Ashihara Eishi
Publication year - 2015
Publication title -
arthritis and rheumatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.106
H-Index - 314
eISSN - 2326-5205
pISSN - 2326-5191
DOI - 10.1002/art.39270
Subject(s) - synovial fluid , gene knockdown , intracellular , chemistry , transporter , extracellular , gene silencing , apoptosis , small interfering rna , synovial membrane , arthritis , rheumatoid arthritis , inflammation , transfection , microbiology and biotechnology , osteoarthritis , cancer research , medicine , immunology , biochemistry , biology , pathology , gene , alternative medicine
Objective Synovial fluid pH is decreased in patients with rheumatoid arthritis (RA); however, the underlying mechanisms are unclear. We undertook this study to examine the mechanism by which synovial fluid pH is regulated and to explore the possibility of a therapeutic strategy by manipulating this mechanism. Methods We determined the pH and lactate concentration in synovial fluid from 16 RA patients. Cultured synovial fibroblasts (SFs) from the inflamed joints of 9 RA patients (RASFs) were examined for the expression of ion transporters that regulate intracellular and extracellular pH. The ion transporter up‐regulated in RASF lines was then suppressed in RASFs by small interfering RNA (siRNA), and the effect of transfection on viability and proliferation was investigated. Finally, we examined the therapeutic effect of electrotransfer of monocarboxylate transporter 4 (MCT4)–specific siRNA into the articular synovium of mice with collagen‐induced arthritis (CIA). Results Synovial fluid pH correlated inversely with both the Disease Activity Score in 28 joints using the C‐reactive protein level and the synovial fluid lactate levels. RASFs exhibited up‐regulated transcription of MCT4 messenger RNA. MCT4 exported intracellular lactate into the extracellular space. RASFs had significantly higher MCT4 protein levels than did SFs from patients with osteoarthritis. Knockdown of MCT4 induced intrinsic apoptosis of RASFs, thereby inhibiting their proliferation. Moreover, electrotransfer of MCT4‐specific siRNA into the articular synovium of mice with CIA significantly reduced the severity of arthritis. Conclusion RA activity correlated with decreased synovial fluid pH. This may be due to increased MCT4 expression in RASFs. Silencing MCT4 induced apoptosis in RASFs and reduced the severity of CIA, suggesting that MCT4 is a potential therapeutic target for inflammatory arthritis.