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Inhibition of osteoclast differentiation by overexpression of NDRG2 in monocytes

Authors
Kang, KyeongahNam, SorimKim, BomiLim, Ji HyunYang, YoungLee, Myeong-SokLim, Jong-Seok
Issue Date
Dec-2015
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
NDRG2; Osteoclastic cytokines; U937 cells; Osteoclastogenesis
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.468, no.4, pp 611 - 616
Pages
6
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
468
Number
4
Start Page
611
End Page
616
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/10158
DOI
10.1016/j.bbrc.2015.10.167
ISSN
0006-291X
1090-2104
Abstract
N-Myc downstream-regulated gene 2 (NDRG2), a member of the NDRG family of differentiation-related genes, has been characterized as a regulator of dendritic cell differentiation from monocytes, CD34(+) progenitor cells, and myelomonocytic leukemic cells. In this study, we show that NDRG2 overexpression inhibits the differentiation of 1.1937 cells into osteoclasts in response to stimulation with a combination of macrophage colony-stimulating factor (M-CSF) and soluble receptor activator of NF-kappa B ligand (RANKL). U937 cells stably expressing NDRG2 are unable to differentiate into multinucleated osteoclast-like cells and display reduced tartrate-resistant acid phosphatase (TRAP) activity and resorption pit formation. Furthermore, NDRG2 expression significantly suppresses the expression of genes that are crucial for the proliferation, survival, differentiation, and function of osteoclasts, including c-Fos, Atp6v0d2, RANK, and OSCAR. The activation of ERK1/2 and p38 is also inhibited by NDRG2 expression during osteoclastogenesis, and the inhibition of osteoclastogenesis by NDRG2 correlates with the down-regulation of the expression of the transcription factor PU.1. Taken together, our results suggest that the expression of NDRG2 potentially inhibits osteoclast differentiation and plays a role in modulating the signal transduction pathway responsible for osteoclastogenesis. (C) 2015 Elsevier Inc. All rights reserved.
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