Regulation of mechanical stress-induced MMP-13 and ADAMTS-5 expression by RUNX-2 transcriptional factor in SW1353 chondrocyte-like cells

被引:122
作者
Tetsunaga, T. [2 ]
Nishida, K. [1 ]
Furumatsu, T. [2 ]
Naruse, K. [3 ]
Hirohata, S. [4 ]
Yoshida, A. [2 ]
Saito, T. [2 ]
Ozaki, T. [2 ]
机构
[1] Okayama Univ, Dept Human Morphol, Grad Sch Med Dent & Pharmaceut Sci, Okayama 7008558, Japan
[2] Okayama Univ, Dept Orthopaed Surg, Grad Sch Med Dent & Pharmaceut Sci, Okayama 7008558, Japan
[3] Okayama Univ, Dept Cardiovasc Physiol, Grad Sch Med Dent & Pharmaceut Sci, Okayama 7008558, Japan
[4] Okayama Univ, Dept Mol Biol & Biochem, Grad Sch Med Dent & Pharmaceut Sci, Okayama 7008558, Japan
关键词
Chondrocyte; Mechanical stress; RUNX-2; ADAMTS; Aggrecanase; HUMAN ARTICULAR-CARTILAGE; CYCLIC TENSILE STRAIN; GENE-EXPRESSION; MATRIX-METALLOPROTEINASE; IN-VITRO; CHONDROSARCOMA CELLS; DYNAMIC COMPRESSION; ONCOSTATIN-M; OSTEOARTHRITIS; AGGRECANASE;
D O I
10.1016/j.joca.2010.11.004
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Objective: To investigate the mechanism of mechanical stress-induced expression and regulation of aggrecanases and examine the role of runt-related transcription factor 2 (RUNX-2) in chondrocyte-like cells. Methods: SW1353 cells were seeded onto stretch chambers at a concentration of 5 x 10(4) cells/chamber, and a uni-axial cyclic tensile strain (CTS) (0.5 Hz, 10% stretch) was applied for 30 min. Total RNA was extracted, reverse transcribed, and analyzed by polymerase chain reaction (PCR) and real-time PCR. RUNX-2 overexpression and small interfering RNA (siRNA) targeting RUNX-2 were used to investigate the role of RUNX-2 in CTS-induced gene expression. The involvement of diverse mitogen-activated protein kinase (MAPK) pathways in the activation of RUNX-2, MMP-13 and ADAMTS-5 during CTS was examined by Western blotting. Results: CTS induced expression of RUNX-2, MMP-13, ADAMTS-4, -5, and -9. Overexpression of RUNX-2 up-regulated expression of MMP-13 and ADAMTS-5, whereas RUNX-2 siRNA resulted in significant down-regulation of mechanically-induced MMP-13 and ADAMTS-5 expression. CTS induced activation of p38 MAPK, and CTS induction of RUNX-2. MMP-13 and ADAMTS-5 mRNA was down-regulated by the selective p38 MAPK inhibitor SB203580 but not by the p44/42 MAPK inhibitor U0126, or the JNK MAPK inhibitor JNK inhibitor II. Conclusions: RUNX-2 might have a role as a key downstream mediator of p38's ability to regulate mechanical stress-induced MMP-13 and ADAMTS-5 expression. (C) 2010 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:222 / 232
页数:11
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