Modeling Parkinson's Disease Using Patient-specific Induced Pluripotent Stem Cells

被引:31
作者
Li, Hong [1 ,2 ]
Jiang, Houbo [1 ,2 ]
Zhang, Boyang [1 ,2 ]
Feng, Jian [1 ,2 ]
机构
[1] Vet Affairs Western New York Healthcare Sys, Buffalo, NY USA
[2] SUNY Buffalo, Dept Physiol & Biophys, Buffalo, NY 14214 USA
关键词
iPSC; pluripotent; stem cells; dopaminergic neurons; parkin; alpha-synuclein; PINK1; DJ-1; LRRK2; GBA; MICROGLIA-LIKE CELLS; G51D SNCA MUTATION; XENO-FREE CULTURE; ALPHA-SYNUCLEIN; DOPAMINE NEURONS; SUBSTANTIA-NIGRA; EARLY-ONSET; ANIMAL-MODELS; FAMILIAL PARKINSONISM; GENETIC CORRECTION;
D O I
10.3233/JPD-181353
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Parkinson's disease (PD) is the second most common neurodegenerative disorder. It is characterized by the degeneration of nigral dopaminergic (DA) neurons. While over 90% of cases are idiopathic, without a clear etiology, mutations in many genes have been linked to rare, familial forms of PD. It has been quite challenging to develop effective animal models of PD that capture salient features of PD. The discovery of induced pluripotent stem cells (iPSCs) makes it possible to generate patient-specific DA neurons to study PD. Here, we review the methods for the generation of iPSCs and discuss previous studies using iPSC-derived neurons from monogenic forms of PD. These investigations have revealed several converging pathways that intersect with the unique vulnerabilities of human nigral DA neurons. With the rapid development in stem cell biology, it is possible to generate patient-specific neurons that will be increasingly similar to those in the brain of the patient. Combined with the ability to edit the genome to generate isogenic iPSCs, the generation and analysis of patient-specific midbrain DA neurons will transform PD research by providing a valuable tool for mechanistic study and drug discovery.
引用
收藏
页码:479 / 493
页数:15
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