Stem cell models of Alzheimer's disease: progress and challenges

被引:91
作者
Arber, Charles [1 ]
Lovejoy, Christopher [1 ]
Wray, Selina [1 ]
机构
[1] UCL Inst Neurol, Dept Mol Neurosci, 1 Wakefield St, London WC1N 1PJ, England
来源
ALZHEIMERS RESEARCH & THERAPY | 2017年 / 9卷
基金
英国国家替代、减少和改良动物研究中心;
关键词
Alzheimer's disease; Induced pluripotent stem cells; Neuronal differentiation; 3D cerebral organoids; CEREBRAL-CORTEX DEVELOPMENT; GAMMA-SECRETASE ACTIVITY; INTRACELLULAR A-BETA; BLOOD-BRAIN-BARRIER; AMYLOID-BETA; DIRECTED DIFFERENTIATION; EFFICIENT DERIVATION; SELF-ORGANIZATION; COMMON VARIANTS; CULTURE MODEL;
D O I
10.1186/s13195-017-0268-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A major challenge to our understanding of the molecular mechanisms of Alzheimer's disease (AD) has been the lack of physiologically relevant in vitro models which capture the precise patient genome, in the cell type of interest, with physiological expression levels of the gene(s) of interest. Induced pluripotent stem cell (iPSC) technology, together with advances in 2D and 3D neuronal differentiation, offers a unique opportunity to overcome this challenge and generate a limitless supply of human neurons for in vitro studies. iPSC-neuron models have been widely employed to model AD and we discuss in this review the progress that has been made to date using patient-derived neurons to recapitulate key aspects of AD pathology and how these models have contributed to a deeper understanding of AD molecular mechanisms, as well as addressing the key challenges posed by using this technology and what progress is being made to overcome these. Finally, we highlight future directions for the use of iPSC-neurons in AD research and highlight the potential value of this technology to neurodegenerative research in the coming years.
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页数:17
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