Combs Benjamin, Kneynsberg Andrew, Kanaan Nicholas M
Department of Translational Science and Molecular Medicine, College of Human Medicine, Michigan State University, 333 Bostwick Avenue NE, Grand Rapids, MI, 49503, USA.
Neuroscience Program, Michigan State University, Grand Rapids, MI, USA.
Methods Mol Biol. 2016;1382:339-66. doi: 10.1007/978-1-4939-3271-9_25.
Dementias are among the most common neurological disorders, and Alzheimer's disease (AD) is the most common cause of dementia worldwide. AD remains a looming health crisis despite great efforts to learn the mechanisms surrounding the neuron dysfunction and neurodegeneration that accompanies AD primarily in the medial temporal lobe. In addition to AD, a group of diseases known as frontotemporal dementias (FTDs) are degenerative diseases involving atrophy and degeneration in the frontal and temporal lobe regions. Importantly, AD and a number of FTDs are collectively known as tauopathies due to the abundant accumulation of pathological tau inclusions in the brain. The precise role tau plays in disease pathogenesis remains an area of strong research focus. A critical component to effectively study any human disease is the availability of models that recapitulate key features of the disease. Accordingly, a number of animal models are currently being pursued to fill the current gaps in our knowledge of the causes of dementias and to develop effective therapeutics. Recent developments in gene therapy-based approaches, particularly in recombinant adeno-associated viruses (rAAVs), have provided new tools to study AD and other related neurodegenerative disorders. Additionally, gene therapy approaches have emerged as an intriguing possibility for treating these diseases in humans. This chapter explores the current state of rAAV models of AD and other dementias, discuss recent efforts to improve these models, and describe current and future possibilities in the use of rAAVs and other viruses in treatments of disease.
痴呆症是最常见的神经疾病之一,而阿尔茨海默病(AD)是全球痴呆症最常见的病因。尽管人们付出巨大努力来了解主要发生在内侧颞叶的、伴随AD出现的神经元功能障碍和神经退行性变的机制,但AD仍然是一个迫在眉睫的健康危机。除了AD,一组被称为额颞叶痴呆(FTDs)的疾病是涉及额叶和颞叶区域萎缩与变性的退行性疾病。重要的是,由于大脑中病理性tau包涵体的大量积累,AD和一些FTDs统称为tau蛋白病。tau蛋白在疾病发病机制中的确切作用仍然是一个重点研究领域。有效研究任何人类疾病的一个关键因素是要有能够重现该疾病关键特征的模型。因此,目前正在探索多种动物模型,以填补我们目前在痴呆症病因知识方面的空白,并开发有效的治疗方法。基于基因治疗的方法,特别是重组腺相关病毒(rAAVs)方面的最新进展,为研究AD和其他相关神经退行性疾病提供了新工具。此外,基因治疗方法已成为治疗人类这些疾病的一种引人关注的可能性。本章探讨了AD和其他痴呆症的rAAV模型的现状,讨论了最近改进这些模型的努力,并描述了在疾病治疗中使用rAAVs和其他病毒的当前及未来可能性。