Generation of neural progenitor cells by chemical cocktails and hypoxia

被引:182
作者
Cheng, Lin [1 ]
Hu, Wenxiang [1 ]
Qiu, Binlong [1 ]
Zhao, Jian [1 ]
Yu, Yongchun [2 ,3 ]
Guan, Wuqiang [2 ,3 ]
Wang, Min [2 ,3 ]
Yang, Wuzhou [2 ,3 ]
Pei, Gang [1 ,4 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, State Key Lab Cell Biol, Shanghai 200031, Peoples R China
[2] Fudan Univ, Inst Neurobiol, Inst Brain Sci, Shanghai 200032, Peoples R China
[3] Fudan Univ, State Key Lab Med Neurobiol, Shanghai 200032, Peoples R China
[4] Tongji Univ, Sch Life Sci & Technol, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
lineage conversion; neural progenitor cells; chemical cocktails; hypoxia; PLURIPOTENT STEM-CELLS; MOUSE FIBROBLASTS; DIRECT CONVERSION; SOMATIC-CELLS; ACTIVATION; GENES; FATE; INDUCTION; OXYGEN;
D O I
10.1038/cr.2014.32
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neural progenitor cells (NPCs) can be induced from somatic cells by defined factors. Here we report that NPCs can be generated from mouse embryonic fibroblasts by a chemical cocktail, namely VCR (V, VPA, an inhibitor of HDACs; C, CHIR99021, an inhibitor of GSK-3 kinases and R, Repsox, an inhibitor of TGF-beta pathways), under a physiological hypoxic condition. These chemical-induced NPCs (ciNPCs) resemble mouse brain-derived NPCs regarding their proliferative and self-renewing abilities, gene expression profiles, and multipotency for different neuroectodermal lineages in vitro and in vivo. Further experiments reveal that alternative cocktails with inhibitors of histone deacetylation, glycogen synthase kinase, and TGF-beta pathways show similar efficacies for ciNPC induction. Moreover, ciNPCs can also be induced from mouse tail-tip fibroblasts and human urinary cells with the same chemical cocktail VCR. Thus our study demonstrates that lineage-specific conversion of somatic cells to NPCs could be achieved by chemical cocktails without introducing exogenous factors.
引用
收藏
页码:665 / 679
页数:15
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