Role of microRNA-129-5p in osteoblast differentiation from bone marrow mesenchymal stem cells

被引:34
作者
Xiao, W. Z. [1 ]
Gu, X. C. [2 ]
Hu, B. [3 ]
Liu, X. W. [4 ]
Zi, Y. [5 ]
Li, M. [2 ]
机构
[1] Fudan Univ, Shanghai Pudong Hosp, Dept Neurol, Shanghai 201399, Peoples R China
[2] Second Mil Med Univ, Changhai Hosp, Dept Orthoped, Shanghai 200433, Peoples R China
[3] Shanghai Minhang Dist Hosp Tradit Chinese Med, Dept Med Oncol, Shanghai 201100, Peoples R China
[4] Shenyang Mil Area Command Chinese PLA, Dept Orthoped, Gen Hosp, Rescue Ctr Severe Wound & Trauma Chinese PLA, Shenyang 110016, Liaoning, Peoples R China
[5] PLA, Dept Emergency, Hosp 463, Shenyang 110042, Peoples R China
关键词
Bone marrow; Mesenchymal stem cells; Osteoblast differentiation; microRNA; DOWN-REGULATING STAT1; STROMAL CELLS; BMP-2; TRANSCRIPTION; PROTECT; TARGETS; RATS;
D O I
10.14715/cmb/2016.62.3.16
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Mesenchymal stem cells derived from bone marrow have the capacity to differentiate into osteoblast, chondrocyte, nerve cell and myocardial cell in vitro, which are an ideal engraft in tissue-engineered repair. Osteoblast differentiation is a vital process in maintaining bone homeostasis in which various transcriptional factors, including signaling molecules, and microRNAs (miRNAs). In this research, human bone marrow mesenchymal stem cells (hBMSCs) were induced differentiation into osteoblast in vitro after over-expression of miR-129-5p. The results showed that the hBMSCs could induce differentiation into osteoblast under the special condition medium, but when the miR-129-5p was over-expressed in hBMSCs, the differentiated efficiency and induced time of osteoblast from hBMSCs could be promoted. This reason was demonstrated that signal transducer and activator of transcription 1 (STAT1) was a transcriptional repressor of osteoblast gene (Runx 2) expression during osteoblast differentiation, miR-129-5p reduced STAT1 levels, leading to the accumulation of correctly spliced Runx 2 mRNA and a dramatic increase in Runx 2 protein.
引用
收藏
页码:95 / 99
页数:5
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