Expression of MicroRNA-146a in Osteoarthritis Cartilage

被引:294
作者
Yamasaki, Keiichiro
Nakasa, Tomoyuki [1 ]
Miyaki, Shigeru [2 ]
Ishikawa, Masakazu
Deie, Masataka
Adachi, Nobuo
Yasunaga, Yuji
Asahara, Hiroshi [2 ,3 ]
Ochi, Mitsuo
机构
[1] Hiroshima Univ, Dept Orthopaed Surg, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348551, Japan
[2] Scripps Res Inst, La Jolla, CA USA
[3] Natl Res Inst Child Hlth & Dev, Bethesda, MD USA
来源
ARTHRITIS AND RHEUMATISM | 2009年 / 60卷 / 04期
关键词
RHEUMATOID-ARTHRITIS; ARTICULAR-CARTILAGE; HUMAN CHONDROCYTES; SYNOVIAL TISSUE; CLASSIFICATION; CRITERIA; DISEASE; PLAYERS; LESIONS; CELLS;
D O I
10.1002/art.24404
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. A role of microRNA, which are similar to 22-nucleotide noncoding RNAs, has recently been recognized in human diseases. The objective of this study was to identify the expression pattern of microRNA-146a (miR-146a) in cartilage from patients with osteoarthritis (OA). Methods. The expression of miR-146a in cartilage from 15 patients with OA was analyzed by quantitative reverse transcription-polymerase chain reaction (RTPCR) and by in situ hybridization. Induction of the expression of miR-146a by cultures of normal human articular chondrocytes following stimulation with interieukin-1 beta (IL-1 beta) was examined by quantitative RT-PCR. Results. All cartilage samples were divided into 3 groups according to a modification of the Mankin score (grade I = mild OA scored 0-5, grade 11 = moderate OA scored 6-10, and grade III = severe OA scored 11.44). In grade I OA cartilage samples, the expression of miR-146a and COL2A1 was significantly higher than that in the other groups (P < 0.05). In grades 11 and III OA cartilage, the expression of miR-146a and COL2A1 was decreased, whereas the expression of matrix metalloproteinase 13 (MMP-13) was elevated in grade 11 OA cartilage. These data showed that miR-146a is expressed intensely in cartilage with a low Mankin grade and that miR-146a expression decreases in parallel with the level of MMP-13 expression. Tissue section in situ hybridization of primary miR-146a (pri-miR-146a) revealed that pri-miR-146a was expressed in chondrocytes residing in all tissue layers, especially in the superficial layer, where it was intensely expressed. The expression of miR-146 was markedly elevated by IL-10 stimulation in human chondrocytes in vitro. Conclusion. This study shows that miR-146 is intensely expressed in low-grade OA cartilage and that its expression is induced by stimulation of IL-1 beta. Thus, miR-146 might play a role in OA cartilage pathogenesis.
引用
收藏
页码:1035 / 1041
页数:7
相关论文
共 35 条
[1]  
ADAMS ME, 1989, J RHEUMATOL, V16, P818
[2]   Il-1β and BMPS -: Interactive players of cartilage matrix degradation and regeneration [J].
Aigner, Thomas ;
Soeder, Stephan ;
Haag, Jochen .
EUROPEAN CELLS & MATERIALS, 2006, 12 :49-56
[3]   THE AMERICAN-COLLEGE-OF-RHEUMATOLOGY CRITERIA FOR THE CLASSIFICATION AND REPORTING OF OSTEOARTHRITIS OF THE HIP [J].
ALTMAN, R ;
ALARCON, G ;
APPELROUTH, D ;
BLOCH, D ;
BORENSTEIN, D ;
BRANDT, K ;
BROWN, C ;
COOKE, TD ;
DANIEL, W ;
FELDMAN, D ;
GREENWALD, R ;
HOCHBERG, M ;
HOWELL, D ;
IKE, R ;
KAPILA, P ;
KAPLAN, D ;
KOOPMAN, W ;
MARINO, C ;
MCDONALD, E ;
MCSHANE, DJ ;
MEDSGER, T ;
MICHEL, B ;
MURPHY, WA ;
OSIAL, T ;
RAMSEYGOLDMAN, R ;
ROTHSCHILD, B ;
WOLFE, F .
ARTHRITIS AND RHEUMATISM, 1991, 34 (05) :505-514
[4]   DEVELOPMENT OF CRITERIA FOR THE CLASSIFICATION AND REPORTING OF OSTEOARTHRITIS - CLASSIFICATION OF OSTEOARTHRITIS OF THE KNEE [J].
ALTMAN, R ;
ASCH, E ;
BLOCH, D ;
BOLE, G ;
BORENSTEIN, D ;
BRANDT, K ;
CHRISTY, W ;
COOKE, TD ;
GREENWALD, R ;
HOCHBERG, M ;
HOWELL, D ;
KAPLAN, D ;
KOOPMAN, W ;
LONGLEY, S ;
MANKIN, H ;
MCSHANE, DJ ;
MEDSGER, T ;
MEENAN, R ;
MIKKELSEN, W ;
MOSKOWITZ, R ;
MURPHY, W ;
ROTHSCHILD, B ;
SEGAL, M ;
SOKOLOFF, L ;
WOLFE, F .
ARTHRITIS AND RHEUMATISM, 1986, 29 (08) :1039-1049
[5]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[6]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[7]  
BHAUMIK D, 2008, ONCOGENE
[8]  
BLANCO FJ, 1995, AM J PATHOL, V146, P75
[9]   The developmental genetics of congenital heart disease [J].
Bruneau, Benoit G. .
NATURE, 2008, 451 (7181) :943-948
[10]  
BULSTRA SK, 1989, CLIN ORTHOP RELAT R, P294