MicroRNA-125b regulates the expression of aggrecanase-1 (ADAMTS-4) in human osteoarthritic chondrocytes

被引:88
|
作者
Matsukawa, Tetsuya [1 ,2 ]
Sakai, Tadahiro [1 ]
Yonezawa, Tomo [2 ,3 ]
Hiraiwa, Hideki [1 ]
Hamada, Takashi [1 ]
Nakashima, Motoshige [1 ]
Ono, Yohei [1 ]
Ishizuka, Shinya [1 ]
Nakahara, Hiroyuki [2 ]
Lotz, Martin K. [2 ]
Asahara, Hiroshi [2 ,4 ]
Ishiguro, Naoki [1 ]
机构
[1] Nagoya Univ, Grad Sch Med, Dept Orthopaed Surg, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
[3] Tokyo Med & Dent Univ, Dept Syst Biomed, Bunkyo Ku, Tokyo 1138510, Japan
[4] Natl Res Inst Child Hlth & Dev, Dept Syst Biomed, Setagaya Ku, Tokyo 1578535, Japan
基金
日本学术振兴会;
关键词
NECROSIS-FACTOR-ALPHA; CARTILAGE; INTERLEUKIN-1; COLLAGEN; BIOGENESIS; INHIBITOR; APOPTOSIS; ROLES; MODEL; RNAS;
D O I
10.1186/ar4164
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Increased expression of aggrecanase-1 (ADAMTS-4) has emerged as an important factor in osteoarthritis (OA) and other joint diseases. This study aimed to determine whether the expression of ADAMTS-4 in human chondrocytes is regulated by miRNA. Methods: MiRNA targets were identified using bioinformatics. Chondrocytes were isolated from knee cartilage and treated with interleukin-1 beta (IL-1 beta). Gene expression was quantified using TaqMan assays and protein production was determined by immunoblotting. Luciferase reporter assay was used to verify interaction between miRNA and target messenger RNA (mRNA). Results: In silico analysis predicted putative target sequence of miR-125b on ADAMTS-4. MiR-125b was expressed in both normal and OA chondrocytes, with significantly lower expression in OA chondrocytes than in normal chondrocytes. Furthermore, IL-1 beta-induced upregulation of ADAMTS-4 was suppressed by overexpression of miR-125b in human OA chondrocytes. In the luciferase reporter assay, mutation of the putative miR-125b binding site in the ADAMTS-4 3'UTR abrogated the suppressive effect of miR125. Conclusions: Our results indicate that miR-125b plays an important role in regulating the expression of ADAMTS-4 in human chondrocytes and this identifies miR-125b as a novel therapeutic target in OA.
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页数:11
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