Transient folate deprivation in combination with small-molecule compounds facilitates the generation of somatic cell-derived pluripotent stem cells in mice.
10.1007/s11596-014-1249-5
- Author:
Wen-tao HU
1
;
Qiu-yue YAN
;
Yu FANG
;
Zhan-dong QIU
;
Su-ming ZHANG
Author Information
1. Department of Neurology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China, zz01hwt@163.com.
- Publication Type:Journal Article
- MeSH:
Amides;
pharmacology;
Animals;
Butyric Acid;
pharmacology;
Cell Differentiation;
drug effects;
Cell Line;
Cell Proliferation;
drug effects;
Extraembryonic Membranes;
cytology;
drug effects;
Folic Acid;
pharmacology;
Induced Pluripotent Stem Cells;
cytology;
drug effects;
Kruppel-Like Transcription Factors;
metabolism;
Mice;
Octamer Transcription Factor-3;
metabolism;
Proto-Oncogene Proteins c-myc;
metabolism;
Pyrazoles;
pharmacology;
Pyridines;
pharmacology;
Pyrimidines;
pharmacology;
SOXB1 Transcription Factors;
metabolism;
Thiocarbamates;
pharmacology;
Thiosemicarbazones
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2014;34(2):151-156
- CountryChina
- Language:English
-
Abstract:
Induced pluripotent stem cells (iPSCs) can be propagated indefinitely, while maintaining the capacity to differentiate into all cell types in the body except for the extra-embryonic tissues. This iPSC technology not only represents a new way to use individual-specific stem cells for regenerative medicine but also constitutes a novel method to obtain large numbers of disease-specific cells for biomedical research. However, the low efficiency of reprogramming and genomic integration of oncogenes and viral vectors limit the potential application of iPSCs. Chemical-induced reprogramming offers a novel approach to generating iPSCs. In this study, a new combination of small-molecule compounds (SMs) (sodium butyrate, A-83-01, CHIR99021, Y-27632) under conditions of transient folate deprivation was used to generate iPSC. It was found that transient folate deprivation combined with SMs was sufficient to permit reprogramming from mouse embryonic fibroblasts (MEFs) in the presence of transcription factors, Oct4 and Klf4, within 25 days, replacing Sox2 and c-Myc, and accelerated the generation of mouse iPSCs. The resulting cell lines resembled mouse embryonic stem (ES) cells with respect to proliferation rate, morphology, pluripotency-associated markers and gene expressions. Deprivation of folic acid, combined with treating MEFs with SMs, can improve the inducing efficiency of iPSCs and reduce their carcinogenicity and the use of exogenous reprogramming factors.
