MicroRNA profiling analysis revealed different cellular senescence mechanisms in human mesenchymal stem cells derived from different origin

被引:27
作者
Meng, Xianhui [1 ]
Xue, Mengying [1 ]
Xu, Peng [1 ]
Hu, Feihu [1 ]
Sun, Bo [1 ]
Xiao, Zhongdang [1 ]
机构
[1] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, Nanjing 210096, Jiangsu, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
MicroRNA; Mesenchymal stem cell; Senescence; Umbilical cord; Cord blood; UMBILICAL-CORD; CANCER CELLS; BONE-MARROW; EXPRESSION; TRANSITION; DISEASE; MATRIX;
D O I
10.1016/j.ygeno.2017.02.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Mesenchymal stem cells (MSCs) from human umbilical cord (UC) and cord blood (CB) share many common properties and exhibit promising clinical potential. Cellular senescence, which induces the loss of stemcells characters and disrupts their therapeutic functions, has been demonstrated to be under the regulation of microRNAs (miRNAs). In this study, we compared the miRNA profiles in early and late passage UCMSCs and CBMSCs based on deep sequencing. 224 and 170 miRNAs were significantly altered in UCMSCs and CBMSCs respectively. A functional annotation of the predicted miRNA targets revealed a series of common senescence pathways. However, Functional enrichment analysis revealed different bioprocesses involved in cellular senescence of UC- and CBMSCs. The common miRNAs shared by the two kinds of MSCs also exert different function in terms of GO enrichment analysis. Our results supported MSCs derived from different origin may undergo senescence through different path. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:147 / 157
页数:11
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