Direct Reprogramming of Mouse and Human Fibroblasts into Multipotent Neural Stem Cells with a Single Factor

被引:424
|
作者
Ring, Karen L. [1 ,3 ]
Tong, Leslie M. [1 ,3 ]
Balestra, Maureen E. [1 ,2 ]
Javier, Robyn [1 ,3 ]
Andrews-Zwilling, Yaisa [1 ,4 ]
Li, Gang [1 ]
Walker, David [1 ,2 ]
Zhang, William R. [1 ]
Kreitzer, Anatol C. [1 ,3 ,4 ]
Huang, Yadong [1 ,2 ,3 ,4 ,5 ]
机构
[1] Gladstone Inst Neurol Dis, San Francisco, CA 94158 USA
[2] Gladstone Inst Cardiovasc Dis, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Biomed Sci Grad Program, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
ADULT HUMAN FIBROBLASTS; HUMAN SOMATIC-CELLS; DIRECT CONVERSION; DOPAMINERGIC-NEURONS; FUNCTIONAL-NEURONS; DIFFERENTIATION; PLURIPOTENCY; GENERATION; INDUCTION; EXPRESSION;
D O I
10.1016/j.stem.2012.05.018
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The generation of induced pluripotent stem cells (iPSCs) and induced neuronal cells (iNCs) from somatic cells provides new avenues for basic research and potential transplantation therapies for neurological diseases. However, clinical applications must consider the risk of tumor formation by iPSCs and the inability of iNCs to self-renew in culture. Here we report the generation of induced neural stem cells (iNSCs) from mouse and human fibroblasts by direct reprogramming with a single factor, Sox2. iNSCs express NSC markers and resemble wild-type NSCs in their morphology, self-renewal, ability to form neurospheres, and gene expression profiles. Cloned iNSCs differentiate into several types of mature neurons, as well as astrocytes and oligodendrocytes, indicating multipotency. Implanted iNSCs can survive and integrate in mouse brains and, unlike iPSC-derived NSCs, do not generate tumors. Thus, self-renewable and multipotent iNSCs without tumorigenic potential can be generated directly from fibroblasts by reprogramming.
引用
收藏
页码:100 / 109
页数:10
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