Contribution of Human Pluripotent Stem Cell-Based Models to Drug Discovery for Neurological Disorders

被引:9
作者
Benchoua, Alexandra [1 ,2 ]
Lasbareilles, Marie [1 ,3 ]
Tournois, Johana [2 ]
机构
[1] ISTEM, CECS, AFM, Neuroplast & Therapeut, F-91100 Corbeil Essonnes, France
[2] ISTEM, CECS, AFM, High Throughput Screening Platform, F-91100 Corbeil Essonnes, France
[3] ISTEM, AFM, UEVE, UMR 861, F-91100 Corbeil Essonnes, France
关键词
pluripotent stem cells; high-throughput screening; drug discovery; precision medicine; neurodegenerative diseases; psychiatric diseases; rare diseases; neurons; glia; LESCH-NYHAN-DISEASE; ADULT HIPPOCAMPAL NEUROGENESIS; IPSC-DERIVED NEURONS; MICROGLIA-LIKE CELLS; ALPHA-SYNUCLEIN; S-ADENOSYLMETHIONINE; DIRECTED DIFFERENTIATION; DOPAMINERGIC-NEURONS; PARKINSONS-DISEASE; EFFICIENT GENERATION;
D O I
10.3390/cells10123290
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
One of the major obstacles to the identification of therapeutic interventions for central nervous system disorders has been the difficulty in studying the step-by-step progression of diseases in neuronal networks that are amenable to drug screening. Recent advances in the field of human pluripotent stem cell (PSC) biology offers the capability to create patient-specific human neurons with defined clinical profiles using reprogramming technology, which provides unprecedented opportunities for both the investigation of pathogenic mechanisms of brain disorders and the discovery of novel therapeutic strategies via drug screening. Many examples not only of the creation of human pluripotent stem cells as models of monogenic neurological disorders, but also of more challenging cases of complex multifactorial disorders now exist. Here, we review the state-of-the art brain cell types obtainable from PSCs and amenable to compound-screening formats. We then provide examples illustrating how these models contribute to the definition of new molecular or functional targets for drug discovery and to the design of novel pharmacological approaches for rare genetic disorders, as well as frequent neurodegenerative diseases and psychiatric disorders.
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页数:25
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