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High extracellular calcium-induced NFATc3 regulates the expression of receptor activator of NF-kappa B ligand in osteoblasts

Cited 25 time in Web of Science Cited 26 time in Scopus
Authors
Lee, Hye-Lim; Bae, On-Yu; Baek, Kyung Hwa; Kwon, Arang; Qadir, Abdul S.; Woo, Kyung Mi; Baek, Jeong-Hwa; Ryoo, Hyun-Mo; Park, Hyun-Jung; Hwang, Hyo Rin
Issue Date
2011-08
Publisher
ELSEVIER SCIENCE INC
Citation
BONE; Vol.49, No.2, pp.242-249
Keywords
OsteoblastsHigh extracellular calciumCalcineurinRANKLNFATc3NFATc1
Abstract
Nuclear factor of activated T cell (NFAT) is a key transcription factor for receptor activator of NF-kappa B ligand (RANKL)-induced osteoclast differentiation. However, it is unclear whether NFAT plays a role in the expression of RANKL in osteoblasts. High extracellular calcium ([Ca(2+)](o)) increases intracellular calcium, enhances RANKL expression in osteoblasts/stromal cells, and induces osteoclastogenesis in a coculture of osteoblasts and hematopoietic bone marrow cells. Because intracellular calcium signaling activates the calcineurin/NFAT pathway, we examined the role of NFAT activation on high [Ca(2+)](o)-induced RANKL expression in MC3T3-E1 subclone 4 (MC4) cells. Among the family of NFAT transcription factors, expression of NFATc1 and NFATc3, but not NFATc2, NFATc4 or NFAT5, was observed in MC4 cells. High [Ca(2+)](o) increased the expression levels of NFATc1, NFATc3 and RANKL. Cyclosporin A and FK506, inhibitors of calcineurin phosphatase, blocked high [Ca(2+)](o)-induced expression of NFAT and RANKL. Knockdown of NFATc1 and NFATc3 by siRNA prevented high [Ca(2+)](o)-induced RANKL expression, whereas overexpression of NFATc1 and NFATc3 induced RANKL expression. Furthermore, overexpressed NFATc1 upregulated NFATc3 expression, but NFATc1 knockdown decreased NFATc3 expression. Chromatin immunoprecipitation and reporter assay results showed that NFATc3, but not NFATc1, directly binds to the RANKL promoter and stimulates RANKL expression. In summary, these results demonstrate that high [Ca(2+)](o) increases expression of RANKL via activation of the calcineurin/NFAT pathway in osteoblasts. In addition, high [Ca(2+)](o) induces the activation and expression of NFATc1; NFATc3 expression and activity are subsequently increased; and NFATc3 directly binds to the RANKL promoter to increase its expression. (C) 2011 Elsevier Inc. All rights reserved.
ISSN
8756-3282
Language
English
URI
http://hdl.handle.net/10371/80435
DOI
https://doi.org/10.1016/j.bone.2011.04.006
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College of Dentistry/School of Dentistry (치과대학/치의학대학원)Dept. of Dentistry (치의학과)Journal Papers (저널논문_치의학과)
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