miR-146a-5p targets Sirt1 to regulate bone mass

被引:18
|
作者
Zheng, Mingxia [1 ,2 ]
Tan, Junlong [1 ,2 ]
Liu, Xiangning [1 ,2 ]
Jin, Fujun [1 ,2 ,3 ]
Lai, Renfa [1 ,2 ]
Wang, Xiaogang [1 ,2 ,3 ]
机构
[1] Jinan Univ, Affiliated Hosp 1, Clin Res Platform Interdiscipline Stomatol, Guangzhou 510632, Guangdong, Peoples R China
[2] Jinan Univ, Dept Stomatol, Coll Stomatol, Guangzhou 510632, Guangdong, Peoples R China
[3] Beihang Univ, Sch Biol Sci & Med Engn, Beijing Adv Innovat Ctr Big Data Based Precis Med, Beijing 100000, Peoples R China
来源
BONE REPORTS | 2021年 / 14卷
基金
中国国家自然科学基金;
关键词
miR-146a-5p; Sirt1; Osteogenesis; Osteoporosis; MicroRNAs; MICRORNA-146A; CELLS; SCLEROSTIN; ACTIVATION; EXPRESSION; MATURATION; CARTILAGE; PATHWAY; LUPUS;
D O I
10.1016/j.bonr.2021.101013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
MicroRNAs (miRNAs) have been proven to serve as key post-transcriptional regulators, affecting diverse biological processes including osteogenic differentiation and bone formation. Recently, it has been reported that miR-146a-5p affects the activity of both osteoblasts and osteoclasts. However, the target genes of miR-146a-5p in these procedures remain unknown. Here we identify miR-146a-5p as a critical suppressor of osteoblastogenesis and bone formation. We found that miR-146a-5p knockout mice exhibit elevated bone formation and enhanced bone mass in vivo. Consistently, we also found that miR-146a-5p inhibited the osteoblast differentiation of bone marrow mesenchymal stem cells (BMSCs) in vitro. Importantly, we further demonstrated that miR-146a-5p directly targeted Sirt1 to inhibit osteoblast activity. Additionally, we showed that the expression of miR-146a-5p gradually increased in femurs with age not only in female mice but also in female patients, and miR-146a-5p deletion protected female mice from age-induced bone loss. These data suggested that miR-146a-5p has a crucial role in suppressing the bone formation and that inhibition of miR-146a-5p may be a strategy for ameliorating osteoporosis.
引用
收藏
页数:9
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