Dopaminergic differentiation using pluripotent stem cells

被引:5
|
作者
Momcilovic, Olga [1 ]
Montoya-Sack, Justine [1 ]
Zeng, Xianmin [1 ]
机构
[1] Buck Inst Res Aging, N Bay CIRM Shared Res Lab Stem Cells & Aging, Novato, CA 94945 USA
关键词
PARKINSON'S DISEASE; DOPAMINERGIC NEURONS; DIFFERENTIATION; PLURIPOTENT STEM CELLS; DISEASE MODELING; CELL THERAPY; DIRECTED DIFFERENTIATION; EFFICIENT GENERATION; NEURAL PROGENITORS; IPS CELLS; ES CELLS; NEURONS; INDUCTION; MIDBRAIN; CONVERSION; MODEL;
D O I
10.1002/jcb.24251
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Parkinson's disease (PD) is the second most common neurodegenerative disorder. The motor symptoms of PD are caused by the loss of dopaminergic (DA) neurons in the substantia nigra pars compacta of mesencephalon. The causes for death of DA neurons are not well understood, but the strongest risk factor is increasing age. There is no cure currently available for PD, and treatment is limited to management of PD symptoms in patients. Primary DA neurons are virtually unobtainable from living patients and animal studies have proven inadequate for studying the mechanism of PD development. Pluripotent stem cells (PSC) are primary self-renewing cells capable of differentiating into all cell types of an organism, including DA neurons. PSCs represent an abundant source of cells that can be genetically modified or isolated from patients with complex diseases, enabling the production of large quantities of DA neurons for disease modeling, drug screening, and gene function studies. Furthermore, since PD arises as a result of deterioration of DA neurons in a specific brain region, it has been suggested that a relatively small number of cells could restore normal function. PSCs could provide a source of DA neurons for cell replacement therapy. In this Prospects article, we focus on the development and in vitro derivation of DA neurons from PSCs, as well as current applications of the technological advances, with the emphasis on future directions and efforts in the field. J. Cell. Biochem. 113: 36103619, 2012. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:3610 / 3619
页数:10
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