Vaspin Attenuates RANKL-Induced Osteoclast Formation in RAW264.7 Cells

被引:42
作者
Kamio, Noriaki [1 ,2 ]
Kawato, Takayuki [3 ,4 ]
Tanabe, Natsuko [3 ,4 ]
Kitami, Satoshi [3 ]
Morita, Toyoko [3 ,5 ]
Ochiai, Kuniyasu [1 ,2 ]
Maeno, Masao [3 ,4 ]
机构
[1] Nihon Univ, Sch Dent, Dept Microbiol, Tokyo 1018310, Japan
[2] Nihon Univ, Sch Dent, Dent Res Ctr, Div Immunol & Pathol, Tokyo 1018310, Japan
[3] Nihon Univ, Sch Dent, Dept Oral Hlth Sci, Tokyo 1018310, Japan
[4] Nihon Univ, Sch Dent, Dent Res Ctr, Div Funct Morphol, Tokyo 1018310, Japan
[5] Lion Fdn Dent Hlth, Tokyo, Japan
关键词
adipokine; osteoclastogenesis; NFATc1; MMP-9; cathepsin K; NF-KAPPA-B; GENE-EXPRESSION; RHEUMATOID-ARTHRITIS; ENDOTHELIAL-CELLS; ADIPOSE-TISSUE; CATHEPSIN-K; OBESITY; NFATC1; DIFFERENTIATION; RECEPTOR;
D O I
10.3109/03008207.2012.761978
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Visceral adipose tissue-derived serine protease inhibitor (vaspin), an adipokine that was recently identified in a rat model of type 2 diabetes, has been suggested to have an insulin-sensitizing effect. In this study, we investigated whether vaspin inhibits receptor activator of nuclear factor-kappa B ligand (RANKL)-induced osteoclastogenesis using two types of osteoclast precursors: RAW264.7 cells and bone marrow cells (BMCs). Vaspin inhibited RANKL-induced osteoclastogenesis in RAW264.7 cells and BMCs. Interestingly, vaspin also inhibited the RANKL-induced expression of nuclear factor of activated T cells c1 (NFATc1) in RAW264.7 cells and BMCs. Furthermore, it inhibited the RANKL-induced upregulation of matrix metalloproteinase-9 and cathepsin K in RAW264.7 cells. Thus, we suggest that vaspin downregulates osteoclastogenesis in part by inhibiting expression of the transcription factor NFATc1.
引用
收藏
页码:147 / 152
页数:6
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