MicroRNA-based system in stem cell reprogramming; differentiation/dedifferentiation

被引:10
|
作者
Pourrajab, Fatemeh [1 ,2 ]
Zarch, Mojtaba Babaei [1 ]
BaghiYazdi, Mohammad [1 ]
Hekmatimoghaddam, Seyedhossein [3 ]
Zare-Khormizi, Mohammad Reza [1 ]
机构
[1] Shahid Sadoughi Univ Med Sci, Sch Med, Yazd, Iran
[2] Shahid Sadoughi Univ Med Sci, Sch Med, Dept Clin Biochem & Mol Biol, Yazd, Iran
[3] Shahid Sadoughi Univ Med Sci, Sch Paramed, Yazd, Iran
关键词
STEM cell; MicroRNA; Cell reprograming; HUMAN EMBRYONIC STEM; ACUTE MYELOID-LEUKEMIA; EPITHELIAL-MESENCHYMAL TRANSITION; RETINAL-PIGMENT EPITHELIUM; TUMOR-SUPPRESSOR; CANCER-CELLS; EPIGENETIC REGULATION; DNA HYPOMETHYLATION; MIR-200; FAMILY; IN-VITRO;
D O I
10.1016/j.biocel.2014.08.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Stem cells (SCs) have self-renew ability and give rise to committed progenitors of a single or multiple lineages. Elucidating the genetic circuits that govern SCs to self-renew and to differentiate is essential to understand the roles of SCs and promise of these cells in regenerative medicine. MicroRNAs are widespread agents playing critical roles in regulatory networks of transcriptional expression and have been strongly linked with SCs for simultaneous maintenance of pluripotency properties such as self-renewal. This review aims to provide state-of-the-art presentations on microRNA-dependent molecular mechanisms contribute to the maintenance of pluripotency. Understanding the microRNA signature interactions, in conjunction with cell signaling, is critical for development of improved strategies to reprogram differentiated cells or direct differentiation of pluripotent cells. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:318 / 328
页数:11
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