CNS disease models with human pluripotent stem cells in the CRISPR age

被引:14
|
作者
Muffat, Julien [1 ]
Li, Yun [1 ]
Jaenisch, Rudolf [1 ]
机构
[1] Whitehead Inst Biomed Res, 9 Cambridge Ctr, Cambridge, MA 02142 USA
关键词
ALZHEIMERS-DISEASE; CEREBRAL ORGANOIDS; HUMAN ES; GENERATION; NEURONS; OLIGODENDROCYTES; FIBROBLASTS; INSIGHTS; DYNAMICS; REVEALS;
D O I
10.1016/j.ceb.2016.10.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In vitro differentiation of human pluripotent stem cells provides a systematic platform to investigate the physiological development and function of the human nervous system, as well as the etiology and consequence when these processes go awry. Recent development in three-dimensional (3D) organotypic culture systems allows modeling of the complex structure formation of the human CNS, and the intricate interactions between various resident neuronal and glial cell types. Combined with an ever-expanding genome editing and regulation toolkit such as CRISPR/Cas9, it is now a possibility to study human neurological disease in the relevant molecular, cellular and anatomical context. In this article, we review recent progress in 3D neural culture and the implications for disease modeling.
引用
收藏
页码:96 / 103
页数:8
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