MiR-124 promotes bone marrow mesenchymal stem cells differentiation into neurogenic cells for accelerating recovery in the spinal cord injury

被引:31
|
作者
Zhao, Yong [1 ]
Jiang, Hui [1 ]
Liu, Xin-Wei [2 ]
Xiang, Liang-Bi [2 ]
Zhou, Da-Peng [2 ]
Chen, Jian-Ting [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Orthoped, Guangzhou 510515, Guangdong, Peoples R China
[2] Chinese PLA, Shenyang Mil Area Command, Gen Hosp, Rescue Ctr Severe Wound & Trauma,Dept Orthoped, Shenyang 110016, Liaoning, Peoples R China
来源
TISSUE & CELL | 2015年 / 47卷 / 02期
关键词
microRNA; Bone marrow; MSCs; Neurogenic cells; NUCLEAR RECEPTOR TLX; NEURONAL DIFFERENTIATION; REGULATORY LOOP; GENE DELIVERY; IN-VITRO; LIVER; LUNG; RATS; TRANSPLANTATION; EXPRESSION;
D O I
10.1016/j.tice.2015.01.007
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
In this research, mouse BMMSCs were isolated from bone marrow, induced to differentiate into neurogenic cells in vitro, and transplanted into the injured spinal cord after over-expression of miR-124. The results showed that the BMMSCs could induce the differentiation to neurogenic cells under the special condition medium, but when the miR-124 was over-expressed, the differentiation efficiency of neurogenic cells from BMMSCs could be promoted. This reason was demonstrated that polypyrimidine tract-binding protein 1 (PTBP1) showed a repressor for polypyrimidine tract-binding protein 2 (PTBP2) during neuronal differentiation, miR-124 reduces PTBP1 levels, leading to the accumulation of correctly spliced PTBP2 mRNA and a dramatic increase in PTBP2 protein. miR-124 promoted neurogenic cells from BMMSCs were successful colonized into injured spinal cord for participation in tissue-repair. In conclusion, our research shows that the miR-124 promoted the differentiation of neuronal cells from BMMSCs, and this mechanism was miR-124 reduced the expression of PTBP1, increased the expression of PTBP2. Copyright (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:140 / 146
页数:7
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