Morton and Gloria Shulman Movement Disorders Centre and the Edmond J Safra Program in Parkinson's Disease, Toronto Western Hospital, Toronto, ONT, Canada.
The Krembil Institute, University Health Network, Toronto, ONT, Canada.
Trends Neurosci. 2016 Nov;39(11):750-762. doi: 10.1016/j.tins.2016.09.003. Epub 2016 Oct 21.
In recent years, a new generation of animal models of Parkinson's disease (PD) based on ectopic expression, overexpression, or intracerebral injection of the protein α-synuclein have emerged. Critically, these models develop inclusions of aggregated α-synuclein and/or α-synuclein-mediated neuronal loss replicating the defining pathological hallmarks of PD and driving significant advances in the understanding of the pathogenic mechanisms underpinning PD. Here, we provide a comprehensive review of this new generation of animal models of PD, ranging from invertebrate to rodent to nonhuman primate. We focus on their strengths and limitations with respect to their highly anticipated contribution to the further understanding of α-synuclein pathobiology and the future testing of novel disease-modifying therapeutics.
近年来,出现了新一代基于α-突触核蛋白异位表达、过表达或脑内注射的帕金森病(PD)动物模型。重要的是,这些模型形成聚集的α-突触核蛋白包涵体和/或α-突触核蛋白介导的神经元丢失,复制了 PD 的明确病理特征,并推动了对 PD 发病机制的深入理解。在这里,我们全面回顾了这新一代的 PD 动物模型,从无脊椎动物到啮齿动物到非人类灵长类动物。我们重点介绍了它们的优缺点,以及它们对进一步了解α-突触核蛋白病理生物学和未来测试新型疾病修饰治疗方法的预期贡献。