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Animal models of Alzheimer's disease and frontotemporal dementia

机译:阿尔茨海默氏病和额颞痴呆的动物模型

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摘要

Insoluble protein aggregates have been linked to Alzheimer's disease (AD) and frontotemporal dementia (FTD). Recent work in transgenic mice has shed light on the role of these aggregates by identifying soluble oligomeric species that may interfere with essential cellular mechanisms at an early disease stage. This review summarizes what we have learned about the roles of these proteins from transgenic mice and invertebrate species such as flies and worms. Proteomic and transcriptomic analyses of tissue from these animal models have identified new molecules with crucial roles in disease. Moreover, transgenic animals have been instrumental in defining drug targets and designing novel therapeutic strategies. With advanced imaging techniques that can be used in both humans and mice an early, preclinical diagnosis of AD and FTD could be within reach.
机译:不溶性蛋白质聚集体与阿尔茨海默氏病(AD)和额颞痴呆(FTD)相关。转基因小鼠的最新工作通过鉴定可在疾病早期阶段干扰基本细胞机制的可溶性寡聚体,阐明了这些聚集体的作用。这篇综述总结了我们从转基因小鼠和无脊椎动物(如苍蝇和蠕虫)中了解到的这些蛋白质的作用。对来自这些动物模型的组织进行的蛋白质组学和转录组学分析已经确定了在疾病中具有关键作用的新分子。此外,转基因动物在定义药物靶标和设计新颖的治疗策略中发挥了作用。借助可用于人类和小鼠的先进成像技术,可以对AD和FTD进行早期的临床前诊断。

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