Comprehensive Perspectives on Experimental Models for Parkinson's Disease

被引:28
作者
Ke, Minjing [1 ]
Chong, Cheong-Meng [1 ]
Zhu, Qi [1 ]
Zhang, Ke [1 ]
Cai, Cui-Zan [1 ]
Lu, Jia-Hong [1 ]
Qin, Dajiang [2 ,3 ]
Su, Huanxing [1 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[2] Guangzhou Med Univ, Affiliated Hosp 1, Guangzhou Regenerat Med & Hlth Guangdong Lab, Guangzhou, Peoples R China
[3] Chinese Acad Sci, Guangzhou Inst Biomed & Hlth, South China Inst Stem Cell Biol & Regenerat Med, Guangzhou, Peoples R China
关键词
Parkinson's disease; experimental model; transgenic animal; cellular model; cross-species model; MUTANT ALPHA-SYNUCLEIN; SH-SY5Y NEUROBLASTOMA-CELLS; POSTNATAL SUBSTANTIA-NIGRA; DOPAMINERGIC NEURONAL LOSS; DROSOPHILA DJ-1 MUTANTS; INDUCED ANIMAL-MODELS; COMPLEX-I INHIBITION; TRANSGENIC MICE; MOUSE MODEL; CAENORHABDITIS-ELEGANS;
D O I
10.14336/AD.2020.0331
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Parkinson's disease (PD) ranks second among the most common neurodegenerative diseases, characterized by progressive and selective loss of dopaminergic neurons. Various cross-species preclinical models, including cellular models and animal models, have been established through the decades to study the etiology and mechanism of the disease from cell lines to nonhuman primates. These models are aimed at developing effective therapeutic strategies for the disease. None of the current models can replicate all major pathological and clinical phenotypes of PD. Selection of the model for PD largely relies on our interest of study. In this review, we systemically summarized experimental PD models, including cellular and animal models used in preclinical studies, to understand the pathogenesis of PD. This review is intended to provide current knowledge about the application of these different PD models, with focus on their strengths and limitations with respect to their contributions to the assessment of the molecular pathobiology of PD and identification of the therapeutic strategies for the disease.
引用
收藏
页码:223 / 246
页数:24
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