Induced Pluripotent Stem Cells and Disorders of the Nervous System: Progress, Problems, and Prospects

被引:8
作者
Faiz, Maryam [1 ]
Nagy, Andras [1 ,2 ,3 ]
机构
[1] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5T 3H7, Canada
[2] Univ Toronto, Dept Obstet & Gynecol, Toronto, ON, Canada
[3] Univ Toronto, Inst Med Sci, Toronto, ON, Canada
关键词
induced pluripotent stem cells (IPSC); reprogramming; neurodegenerative disease; direct cell fate conversion; FAMILIAL ALZHEIMERS-DISEASE; DIRECT CONVERSION; DOPAMINERGIC-NEURONS; MOUSE FIBROBLASTS; COPY NUMBER; DIRECTED DIFFERENTIATION; ES CELLS; IDENTIFICATION; GENERATION; PHENOTYPES;
D O I
10.1177/1073858413493148
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Advances in cellular reprograming have shown that the delivery of specific transcription factors can result in the shift of one cell type to another. Brief forced expression of the four Yamanaka reprogramming factors (Klf4, Sox2, c-Myc, and Oct4) is able to convert many cell types into induced pluripotent stem cells, whereas some lineage specific transcription factors can convert cells from one type directly to another. Numerous strategies have already been developed for deriving neural cell types, with the hopes of better understanding/alleviating neurodegenerative disease. These cells facilitate drug discovery and constitute an autologous source of cells for brain repair, thus, avoiding rejection issues faced by allografts derived from embryonic stem cells. However, proper characterization of the various types of reprogrammed cells and an understanding of how these cells acquire neural fate is necessary before their translation into the clinic. Here, we review the progress, problems, and prospects with reprogrammed cell types with regards to neurodegenerative disease.
引用
收藏
页码:567 / 577
页数:11
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