miR-218 Regulates Glycogen Synthase Kinase-3β and Promotes Differentiation of Human Bone Marrow Mesenchymal Stem Cells into Osteoblasts

被引:1
|
作者
Ling, Long [1 ]
Hu, Hailan [1 ]
Yadav, Ram Ishwar [1 ]
Gao, Jianliang [1 ]
Wei, Xiao [1 ]
Han, Menghu [1 ]
Cao, Yanming [1 ]
机构
[1] Guangzhou Med Univ, Dept Orthoped, Affiliated Hosp 2, Guangzhou 510260, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-218; GSK-3; beta; Wnt/beta-Catenin; Osteogenic Differentiation; SIGNALING PATHWAY; OSTEOGENESIS; CIRCUIT;
D O I
10.1166/jbt.2020.2233
中图分类号
Q813 [细胞工程];
学科分类号
摘要
miR-218 is associated with osteogenesis. Bioinformatics analysis showed a targeting relationship between miR-218 and GSK-3 beta 3'-UTR. Our study assessed whether miR-218 regulates GSK-3 beta expression and affects osteoblast differentiation of bone marrow mesenchymal stem cells (BMSCs). Osteogenic induction medium was used to induce BMSCs to differentiate into osteoblasts. miR-218, GSK-3 beta, beta-catenin and RUNX2 level was detected during D10 and D20 differentiation. BMSCs cells were divided into antagomir-NC and antagomir-218, and induced to differentiate for 20 days followed by analysis of GSK-3 beta, beta-catenin and RUNX2 level, osteogenesis and cell differentiation by the alizarin red staining. Compared with pre-differentiation, the expression of miR-218, beta-catenin and RUNX2 was gradually increased and GSK-3 beta expression was decreased during the differentiation of BMSCs into osteoblasts. There was a targeted regulation relationship between miR-218 and GSK-3 beta. Compared with the antagomir-NC group, GSK-3 beta protein expression was increased in antagomir-218 transfection group, with decreased the expression of beta-catenin and RUNX2 protein, reduced ALP activity as well as weakened staining degree of alizarin red. GSK-3 beta expression is decreased and miR-218 expression is increased during osteoblast differentiation of BMSCs. Inhibition of miR-218 expression can up-regulate GSK-3 beta expression and attenuate the ability of BMSCs to differentiate into osteoblasts.
引用
收藏
页码:176 / 181
页数:6
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