Chemical reprogramming and transdifferentiation

被引:73
|
作者
Xie, Xin [1 ,2 ]
Fu, Yanbin [2 ]
Liu, Jian [1 ]
机构
[1] Chinese Acad Sci, CAS Key Lab Receptor Res, Natl Ctr Drug Screening, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
[2] Tongji Univ, Shanghai Key Lab Signaling & Dis Res, Lab Receptor Based Biomed, Sch Life Sci & Technol, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
PLURIPOTENT STEM-CELLS; MOUSE SOMATIC-CELLS; DIRECT CONVERSION; SMALL MOLECULES; HUMAN FIBROBLASTS; EPITHELIAL-CELLS; PROGENITOR CELLS; INDUCTION; GENERATION; CARDIOMYOCYTES;
D O I
10.1016/j.gde.2017.07.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The revolutionizing somatic cell reprogramming/ transdifferentiation technologies provide a new path for cell replacement therapies and drug screening. The original method for reprogramming involves the delivery of exogenous transcription factors, leading to the safety concerns about the possible genome integration. Many efforts have been taken to avoid genetic alteration in somatic cell reprogramming/ transdifferentiation by using non-integrating gene delivery approaches, cell membrane permeable proteins, and small molecule compounds. Compared to other methods, smallmolecule compounds have several unique advantages, such as structural versatility and being easy to control in a timedependent and concentration-dependent way. More importantly, small molecules have been used as drugs to treat human diseases for thousands of years. So the small molecule approach to reprogramming might be more acceptable in clinical-related uses. In the past few years, small molecule approaches have made significant progresses in inducing pluripotent or functional differentiated cells from somatic cells. Here we review the recent achievements of chemical reprogramming/transdifferentiation and discuss the advantages and challenges facing this strategy in future applications.
引用
收藏
页码:104 / 113
页数:10
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