Deutsches Zentrum für Neurodegenerative Erkrankungen, Standort München, Ludwig-Maximilians University, Munich, Germany.
Neurodegener Dis. 2010;7(1-3):99-102. doi: 10.1159/000285515. Epub 2010 Feb 18.
Our ageing society is confronted with a dramatic increase in patients suffering from tauopathies such as Alzheimer's disease, frontotemporal dementia and others. Typical neuropathological lesions including tangles composed of hyperphosphorylated tau protein as well as severe neuronal cell death characterize these disorders. No mechanism-based cures are available at present. Genetically modified animals are invaluable models to understand the molecular disease mechanisms and to screen for modifying compounds. We recently introduced tau-transgenic zebrafish as a novel model for tauopathies. Our model allows recapitulating key pathological features of tauopathies within an extremely short time. Moreover, life imaging of tau-dependent neuronal cell death was performed for the very first time. This demonstrated tau-dependent neuronal cell loss independent of tangle formation. Finally, we exemplified that the zebrafish frontotemporal dementia model can be used to screen for drugs that prevent abnormal tau phosphorylation and neuronal cell death.
我们的老龄化社会正面临着患tau 病(如阿尔茨海默病、额颞叶痴呆等)的患者数量的急剧增加。这些疾病的典型神经病理学病变包括由过度磷酸化的 tau 蛋白组成的缠结以及严重的神经元细胞死亡。目前尚无基于机制的治疗方法。遗传修饰动物是了解分子疾病机制和筛选修饰化合物的宝贵模型。我们最近引入了转 tau 基因的斑马鱼作为 tau 病的一种新模型。我们的模型允许在极短的时间内重现 tau 病的关键病理特征。此外,还首次进行了 tau 依赖性神经元细胞死亡的生命成像。这证明了tau 依赖性神经元细胞丢失与缠结形成无关。最后,我们举例说明了斑马鱼额颞叶痴呆模型可用于筛选预防异常 tau 磷酸化和神经元细胞死亡的药物。