Modeling neurological diseases using patient-derived induced pluripotent stem cells

被引:31
|
作者
Juopperi, Tarja A. [1 ]
Song, Hongjun [1 ,2 ,3 ]
Ming, Guo-li [1 ,2 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD USA
关键词
disease modeling; human induced pluripotent stem cell; neurobiology; neurodegenerative; neurodevelopmental;
D O I
10.2217/FNL.11.14
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Reprogramming of somatic cells to an embryonic-like state has dramatically changed the landscape of stem cell research. Although still in its formative stages, the field of induced pluripotent stem cells (iPSCs) has the potential to advance the study of neurodegenerative and neurodevelopmental disorders at the molecular and cellular levels. The iPSC technology could be employed to establish in vitro experimental model systems for the identification of molecular lesions and to aid in the discovery of therapeutic targets and effective compounds. The derivation of patient-specific iPSCs has also opened up the possibility of generating disease-relevant cells for toxicity screening and for cellular therapy. In this article, we review the recent progress in the use of disease-specific iPSCs for in vitro and in vivo modeling of neurological diseases.
引用
收藏
页码:363 / 373
页数:11
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