Pluripotent stem cells for neurodegenerative disease modeling: an expert view on their value to drug discovery

被引:9
作者
Chen, Shi-Dong [1 ,2 ]
Li, Hong-Qi [1 ,2 ]
Cui, Mei [1 ,2 ]
Dong, Qiang [1 ,2 ]
Yu, Jin-Tai [1 ,2 ]
机构
[1] Fudan Univ, Shanghai Med Coll, Huashan Hosp, Dept Neurol, 12 Wulumuqi Rd, Shanghai, Peoples R China
[2] Fudan Univ, Shanghai Med Coll, Huashan Hosp, Inst Neurol, Shanghai, Peoples R China
关键词
Human iPS cells; neurodegenerative disease; disease modeling; drug discovery; neuronal subtypes; glial cell; organoid; screening platforms; EFFICIENT NEURAL CONVERSION; HUMAN BRAIN-DEVELOPMENT; IPSC-DERIVED NEURONS; PARKINSONS-DISEASE; MOTOR-NEURONS; DOPAMINERGIC PROGENITORS; GENETIC CORRECTION; HUMAN ES; GENERATION; OLIGODENDROCYTES;
D O I
10.1080/17460441.2020.1767579
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Neurodegenerative diseases have become a major global health concern, posing a huge disease burden on patients and their families. Although there has been rapid progress in the development of therapies, a lack of accurate disease models and efficient drug screening platforms have made achieving a breakthrough difficult. The technology of human-induced pluripotent stem cells (iPSCs) shows better recapitulation of disease pathophysiology and provides a more accessible supply of patient-specific samples compared to other modeling methods. It has been a powerful tool for mechanism exploration and drug development. Areas covered: This review describes the recent use of human iPSC-derived cells for modeling neurodegenerative disorders and discovering potential drugs. Expert opinion: Model systems based on iPSC-derived cells have created a paradigm shift in drug discovery. Accuracy, consistency, translatability, and cost-effectiveness are the four major focuses of academic and industrial communities to fulfill the potential of iPSC technology for their purposes. It is the art of balance between these four factors to generate efficacious outputs with maximum efficiency. Future studies should persist in refining this technology and promote its application in this field to benefit all the disease-affected population eventually.
引用
收藏
页码:1081 / 1094
页数:14
相关论文
共 124 条
[1]   Suberoylanilide hydroxamic acid increases progranulin production in iPSC-derived cortical neurons of frontotemporal dementia patients [J].
Almeida, Sandra ;
Gao, Fuying ;
Coppola, Giovanni ;
Gao, Fen-Biao .
NEUROBIOLOGY OF AGING, 2016, 42 :35-40
[2]   2018 Alzheimer's disease facts and figures [J].
不详 .
ALZHEIMERS & DEMENTIA, 2018, 14 (03) :367-425
[3]  
[Anonymous], CELL STEM CELL, DOI DOI 10.1016/J.STEM.2012.04.027.PUBMED:22748968
[4]   Regulatory-accepted drug development tools are needed to accelerate innovative CNS disease treatments [J].
Arneric, Stephen P. ;
Kern, Volker D. ;
Stephenson, Diane T. .
BIOCHEMICAL PHARMACOLOGY, 2018, 151 :291-306
[5]   The epidemiology of Parkinson's disease: risk factors and prevention [J].
Ascherio, Alberto ;
Schwarzschild, Michael A. .
LANCET NEUROLOGY, 2016, 15 (12) :1255-1270
[6]   Alzheimer's disease [J].
Ballard, Clive ;
Gauthier, Serge ;
Corbett, Anne ;
Brayne, Carol ;
Aarsland, Dag ;
Jones, Emma .
LANCET, 2011, 377 (9770) :1019-1031
[7]   Frontotemporal dementia [J].
Bang, Jee ;
Spina, Salvatore ;
Miller, Bruce L. .
LANCET, 2015, 386 (10004) :1672-1682
[8]   Modeling psychiatric disorders at the cellular and network levels [J].
Brennand, K. J. ;
Simone, A. ;
Tran, N. ;
Gage, F. H. .
MOLECULAR PSYCHIATRY, 2012, 17 (12) :1239-1253
[9]   Phenotypic Screening Identifies Modulators of Amyloid Precursor Protein Processing in Human Stem Cell Models of Alzheimer's Disease [J].
Brownjohn, Philip W. ;
Smith, James ;
Portelius, Erik ;
Serneels, Lutgarde ;
Kvartsberg, Hlin ;
De Strooper, Bart ;
Blennow, Kaj ;
Zetterberg, Henrik ;
Livesey, Frederick J. .
STEM CELL REPORTS, 2017, 8 (04) :870-882
[10]   Dopamine oxidation mediates mitochondrial and lysosomal dysfunction in Parkinson's disease [J].
Burbulla, Lena F. ;
Song, Pingping ;
Mazzulli, Joseph R. ;
Zampese, Enrico ;
Wong, Yvette C. ;
Jeon, Sohee ;
Santos, David P. ;
Blanz, Judith ;
Obermaier, Carolin D. ;
Strojny, Chelsee ;
Savas, Jeffrey N. ;
Kiskinis, Evangelos ;
Zhuang, Xiaoxi ;
Kruger, Rejko ;
Surmeier, D. James ;
Krainc, Dimitri .
SCIENCE, 2017, 357 (6357) :1255-+