MicroRNA-124 regulates osteoclast differentiation

被引:136
作者
Lee, Youngkyun [1 ]
Kim, Hyo Jeong [1 ]
Park, Cheol Kyu [2 ]
Kim, Yong-Gun [3 ]
Lee, Heon-Jin [4 ]
Kim, Jae-Young [1 ]
Kim, Hong-Hee [2 ]
机构
[1] Kyungpook Natl Univ, Dept Biochem, Sch Dent, Taegu 700412, South Korea
[2] Seoul Natl Univ, Dept Cell & Dev Biol, Sch Dent, Seoul 110749, South Korea
[3] Kyungpook Natl Univ, Dept Periodontol, Sch Dent, Taegu 700412, South Korea
[4] Kyungpook Natl Univ, Dept Microbiol, Sch Dent, Taegu 700412, South Korea
基金
新加坡国家研究基金会;
关键词
Osteoclast; miR-124; NFATc1; Differentiation; GLYCOGEN-SYNTHASE KINASE-3; BONE-RESORPTION; HEPATOCELLULAR-CARCINOMA; NEURITE OUTGROWTH; RAW264.7; CELLS; NF-ATC; NFATC1; EXPRESSION; RANKL; INVOLVEMENT;
D O I
10.1016/j.bone.2013.07.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Osteoclasts are specialized cells for bone-resorption originated from precursors of macrophage/monocyte lineage. The receptor activator of NF kappa B ligand (RANKL) initiates osteoclast differentiation, in which nuclear factor of activated T cell cytoplasmic 1 (NFATc1) plays a key role as a master transcription factor. In the present report, we show that microRNA-124 (miR-124) regulates osteoclastogenesis of mouse bone marrow macrophages (BMMs) by suppressing NFATc1 expression. On the other hand, synthetic inhibitor that binds specifically to miR-124 enhanced osteoclast differentiation and NFATc1 expression. The overexpression of a constitutively active form of NFATc1 prevented the inhibitory effect of miR-124 on osteoclastogenesis. Finally, miR-124 also affected the proliferation and motility of osteoclast precursors, the latter coinciding with the reduced expression of RhoA and Rac1. These findings not only reveal unprecedented role of miR-124 in osteoclastogenesis but also suggest a novel mode of regulation of NFATc1 in osteoclasts. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:383 / 389
页数:7
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