The overexpression of SIRT1 inhibited osteoarthritic gene expression changes induced by interleukin-1β in human chondrocytes

被引:114
作者
Matsushita, Takehiko [1 ]
Sasaki, Hiroshi [1 ]
Takayama, Koji [1 ]
Ishida, Kazunari [1 ]
Matsumoto, Tomoyuki [1 ]
Kubo, Seiji [1 ]
Matsuzaki, Tokio [1 ]
Nishida, Kotaro [1 ]
Kurosaka, Masahiro [1 ]
Kuroda, Ryosuke [1 ]
机构
[1] Kobe Univ, Grad Sch Med, Dept Orthopaed Surg, Chuo Ku, Kobe, Hyogo 6500017, Japan
关键词
SIRT1; overexpression; osteoarthritis; chondrocytes; IL-1; beta; FACTOR-KAPPA-B; CELL-SURVIVAL; DEPENDENT TRANSCRIPTION; ARTICULAR CHONDROCYTES; CARTILAGE; APOPTOSIS; PATHOGENESIS; MODULATION; ACTIVATION; ADAMTS5;
D O I
10.1002/jor.22268
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
摘要
In this study, we examined the effects of overexpression of SIRT1 on IL-1-induced gene expression changes in human chondrocytes to explore a protective role of SIRT1 in human chondrocytes. SIRT1 was overexpressed in human chondrocytes by expression plasmid under stimulation with IL-1. SIRT1 was also inhibited by siRNA under stimulation with IL-1. Gene expression changes were examined by real-time PCR. The interaction of SIRT1 and p65 (NF-B) were examined by Western blotting. SIRT1, MMP-13, and ADAMTS-5 expressions in human cartilage were examined by immunohistochemistry. IL-1 stimulation significantly up-regulated MMP-1, 2, 9, and 13 and ADAMTS-5. Overexpression of SIRT1 significantly inhibited the up-regulation of those genes caused by IL-1 while the inhibition of SIRT1 further increased them. In addition, the overexpression of SIRT1 markedly reduced the IL-1-induced acetylation of p65. SIRT1 expression was clearly detected in the non-OA cartilage while MMP-13 and ADAMTS-5 were undetectable. In contrast, in the OA cartilage, SIRT1 expression was decreased while MMP-13 and ADAMTS-5 were increased. Our observations suggested that SIRT1 can play a protective role by suppressing IL-1-induced expressions of cartilage-degrading enzymes partially through the modulation of the NF-B pathway. SIRT1 overexpression might be a new therapeutic approach for OA. (c) 2012 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 31: 531537, 2013
引用
收藏
页码:531 / 537
页数:7
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