Departments of Neuroscience, MRC Centre for Neurodegeneration Research, King's College London, Institute of Psychiatry, De Crespigny Park, UK.
CNS Neurol Disord Drug Targets. 2010 Aug;9(4):403-28. doi: 10.2174/187152710791556131.
Tauopathies, including Alzheimer's disease, are neurodegenerative diseases characterized by the deposition of hyperphosphorylated tau protein in the central nervous system, and are the major cause of dementia in later life. Considerable advances have been made in developing mouse models that recapitulate, to varying extents, the development of human tau pathology, and the learning and memory deficits characteristic of some tauopathies. Furthermore, such models have been used to show promising disease-modifying effects in pre-clinical testing of new therapeutics. Various strategies have been utilised to generate mouse models of tauopathies. Some of the most enlightening models developed to date either constitutively or inducibly express pathogenic tau mutations. These animals have been instrumental in defining critical disease-related mechanisms, including the observation that tangles are not the toxic form of tau in disease. Here, we discuss the strengths and weaknesses of well characterised transgenic models that emulate human tauopathy, and include a comprehensive listing of the main phenotypic characteristics of all reported tau transgenic rodents. We summarise the use of tau mice for the development and evaluation of new therapeutic approaches, and their utility in identifying novel drug targets. In addition, we review the parameters to be considered in the development of the next generation of mouse models of tauopathy, aimed at further increasing our understanding of disease aetiology and in evaluating novel treatments.
tau 病包括阿尔茨海默病,是中枢神经系统中过度磷酸化 tau 蛋白沉积的神经退行性疾病,是晚年痴呆的主要原因。在开发能够在不同程度上重现人类 tau 病理学发展以及某些 tau 病特征性学习和记忆缺陷的小鼠模型方面已经取得了相当大的进展。此外,这些模型已被用于在新疗法的临床前测试中显示出有希望的疾病修饰作用。已经利用了各种策略来生成 tau 病的小鼠模型。迄今为止开发的一些最有启发性的模型要么组成型表达致病性 tau 突变,要么诱导表达致病性 tau 突变。这些动物对于定义关键的疾病相关机制非常重要,包括观察到缠结在疾病中不是 tau 的毒性形式。在这里,我们讨论了模拟人类 tau 病的经过良好表征的转基因模型的优缺点,并列出了所有报道的 tau 转基因啮齿动物的主要表型特征的综合清单。我们总结了 tau 小鼠在开发和评估新治疗方法中的用途,以及它们在鉴定新药物靶点方面的用途。此外,我们回顾了开发下一代 tau 病小鼠模型时要考虑的参数,旨在进一步加深我们对疾病病因的理解,并评估新的治疗方法。