Department of Public Health and Caring Sciences, Molecular Geriatrics, Uppsala University, Uppsala, Sweden.
Krembil Brain Institute, University Health Network, Toronto, Ontario, Canada.
Brain Behav. 2022 Jul;12(7):e2628. doi: 10.1002/brb3.2628. Epub 2022 Jun 1.
Intracellular deposition of alpha-synuclein (α-syn) as Lewy bodies and Lewy neurites is a central event in the pathogenesis of Parkinson's disease (PD) and other α-synucleinopathies. Transgenic mouse models overexpressing human α-syn, are useful research tools in preclinical studies of pathogenetic mechanisms. Such mice develop α-syn inclusions as well as neurodegeneration with a topographical distribution that varies depending on the choice of promoter and which form of α-syn that is overexpressed. Moreover, they display motor symptoms and cognitive disturbances that to some extent resemble the human conditions.
One of the main motives for assessing behavior in these mouse models is to evaluate the potential of new treatment strategies, including their impact on motor and cognitive symptoms. However, due to a high within-group variability with respect to such features, the behavioral studies need to be applied with caution. In this review, we discuss how to make appropriate choices in the experimental design and which tests that are most suitable for the evaluation of PD-related symptoms in such studies.
We have evaluated published results on two selected transgenic mouse models overexpressing wild type (L61) and mutated (A30P) α-syn in the context of their validity and utility for different types of behavioral studies.
By applying appropriate behavioral tests, α-syn transgenic mouse models provide an appropriate experimental platform for studies of symptoms related to PD and other α-synucleinopathies.
α-突触核蛋白(α-syn)在细胞内的沉积形成路易体和路易神经突,是帕金森病(PD)和其他α-突触核蛋白病发病机制的核心事件。过表达人α-syn 的转基因小鼠模型是研究发病机制的临床前研究中的有用研究工具。这些小鼠会产生α-syn 包涵体以及神经退行性变,其分布的拓扑结构取决于启动子的选择和过表达的α-syn 形式。此外,它们还会出现运动症状和认知障碍,在某种程度上类似于人类疾病。
评估这些小鼠模型中行为的主要动机之一是评估新治疗策略的潜力,包括它们对运动和认知症状的影响。然而,由于这些特征在组内存在高度的变异性,因此需要谨慎应用行为研究。在这篇综述中,我们讨论了如何在实验设计中做出适当的选择,以及哪些测试最适合评估此类研究中与 PD 相关的症状。
我们评估了两个选定的转基因小鼠模型的已发表结果,这些模型过表达野生型(L61)和突变型(A30P)α-syn,评估它们在不同类型的行为研究中的有效性和实用性。
通过应用适当的行为测试,α-syn 转基因小鼠模型为研究与 PD 和其他α-突触核蛋白病相关的症状提供了适当的实验平台。