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- W2108703764 abstract "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-κB 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." @default.
- W2108703764 created "2016-06-24" @default.
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- W2108703764 date "2013-01-16" @default.
- W2108703764 modified "2023-10-11" @default.
- W2108703764 title "Vaspin Attenuates RANKL-Induced Osteoclast Formation in RAW264.7 Cells" @default.
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- W2108703764 doi "https://doi.org/10.3109/03008207.2012.761978" @default.
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