miR-483-3p regulates osteogenic differentiation of bone marrow mesenchymal stem cells by targeting STAT1

被引:16
|
作者
Xiao, Ye [1 ]
Guo, Qi [1 ]
Jiang, Tie-Jian [1 ]
Yuan, Ying [1 ]
Yang, Li [1 ]
Wang, Guang-Wei [2 ]
Xiao, Wen-Feng [3 ]
机构
[1] Cent S Univ, Endocrinol Res Ctr, Dept Endocrinol, Changsha 410008, Hunan, Peoples R China
[2] Hunan Univ Med, Dept Med, Huaihua 418000, Hunan, Peoples R China
[3] Cent S Univ, Xiangya Hosp, Dept Orthopaed, 87 Xiangya Rd, Changsha 410008, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
osteogenic differentiation; microRNA-483-3p; STAT1; OSTEOBLAST DIFFERENTIATION; DISRUPTION; EXPRESSION; GENE;
D O I
10.3892/mmr.2019.10700
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) is regulated by a variety of intracellular regulatory factors including osterix, runt-related transcription factor 2 (RUNX2), bone morphogenetic proteins and transforming growth factor beta. Recent studies have shown that microRNAs (miRs) serve a crucial role in this process. In the present study, miR-483-3p levels were significantly increased during osteogenic differentiation of mouse and human BMSCs. Overexpression of miR-483-3p promoted osteogenic differentiation, whereas inhibition of miR-483-3p reversed these effects. miR-483-3p regulated osteogenic differentiation of BMSCs by targeting STAT1, and thus enhancing RUNX2 transcriptional activity and RUNX2 nuclear translocation. In vivo, overexpression of miR-483-3p using a BMSC-specific aptamer delivery system stimulated bone formation in aged mice. Therefore, the present study suggested that miR-483-3p promoted osteogenic differentiation of BMSCs by targeting STAT1, and miR-483-3 prepresent a potential therapeutic target for age-related bone loss.
引用
收藏
页码:4558 / 4566
页数:9
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