New transgenic models of Parkinson's disease using genome editing technology

被引:3
作者
Cota-Coronado, J. A. [1 ]
Sandoval-Avila, S. [1 ]
Gaytan-Davila, Y. P. [1 ]
Diaz, N. F. [2 ]
Vega-Ruiz, B. [3 ]
Padilla-Camberos, E. [1 ]
Diaz-Martinez, N. E. [1 ]
机构
[1] Ctr Invest & Asistencia Tecnol & Diseno Estado Ja, Biotecnol Med & Farmaceut, Guadalajara, Jalisco, Mexico
[2] Inst Nacl Perinatol, Dept Biol Celular, Ciudad De Mexico, Mexico
[3] Univ Guadalajara, Ctr Univ Ciencias Salud, Dept Neurociencias, Guadalajara, Jalisco, Mexico
来源
NEUROLOGIA | 2020年 / 35卷 / 07期
关键词
Transgenic models; Parkinson's disease; Neurodegeneration; Dopaminergic neurons; CRISPR/Cas9; IPSC; PLURIPOTENT STEM-CELLS; MIDBRAIN DOPAMINERGIC-NEURONS; ZINC-FINGER NUCLEASES; ALPHA-SYNUCLEIN; MOUSE MODEL; GENE; CRISPR-CAS9; GENERATION; NEURODEGENERATION; DYSFUNCTION;
D O I
10.1016/j.nrl.2017.08.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Parkinson's disease (PD) is the second most common neurodegenerative disorder. It is characterised by selective loss of dopaminergic neurons in the substantia nigra pars compacta, which results in dopamine depletion, leading to a number of motor and non-motor symptoms. Development: In recent years, the development of new animal models using nuclease-based genome-editing technology (ZFN, TALEN, and CRISPR/Cas9 nucleases) has enabled the introduction of custom-made modifications into the genome to replicate key features of PD, leading to significant advances in our understanding of the pathophysiology of the disease. Conclusions: We review the most recent studies on this new generation of in vitro and in vivo PD models, which replicate the most relevant symptoms of the disease and enable better understanding of the aetiology and mechanisms of PD. This may be helpful in the future development of effective treatments to halt or slow disease progression. (C) 2017 Sociedad Espanola de Neurologia. Published by Elsevier Espana, S.L.U.
引用
收藏
页码:486 / 499
页数:14
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