New pathogenic insights from large animal models of neurodegenerative diseases

被引:33
|
作者
Yin, Peng [1 ]
Li, Shihua [1 ]
Li, Xiao-Jiang [1 ]
Yang, Weili [1 ]
机构
[1] Jinan Univ, Guangdong Hongkong Macau Inst CNS Regenerat, Guangdong Key Lab Nonhuman Primate Res, Guangzhou 510632, Peoples R China
基金
中国国家自然科学基金;
关键词
large animal models; neurodegenerative diseases; CRISPR; Cas9; AMYOTROPHIC-LATERAL-SCLEROSIS; FRONTOTEMPORAL LOBAR DEGENERATION; PARKIN-DEFICIENT MICE; HUNTINGTONS-DISEASE; MOUSE MODELS; HUMAN BRAIN; DEPENDENT NEUROPATHOLOGY; INTRANUCLEAR INCLUSIONS; PINK1/PARKIN MITOPHAGY; PROGENITOR BEHAVIOR;
D O I
10.1007/s13238-022-00912-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Animal models are essential for investigating the pathogenesis and developing the treatment of human diseases. Identification of genetic mutations responsible for neurodegenerative diseases has enabled the creation of a large number of small animal models that mimic genetic defects found in the affected individuals. Of the current animal models, rodents with genetic modifications are the most commonly used animal models and provided important insights into pathogenesis. However, most of genetically modified rodent models lack overt neurodegeneration, imposing challenges and obstacles in utilizing them to rigorously test the therapeutic effects on neurodegeneration. Recent studies that used CRISPR/Cas9-targeted large animal (pigs and monkeys) have uncovered important pathological events that resemble neurodegeneration in the patient's brain but could not be produced in small animal models. Here we highlight the unique nature of large animals to model neurodegenerative diseases as well as the limitations and challenges in establishing large animal models of neurodegenerative diseases, with focus on Huntington disease, Amyotrophic lateral sclerosis, and Parkinson diseases. We also discuss how to use the important pathogenic insights from large animal models to make rodent models more capable of recapitulating important pathological features of neurodegenerative diseases.
引用
收藏
页码:707 / 720
页数:14
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