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Single-nucleus RNA sequencing reveals transcriptional changes of hippocampal neurons in APP23 mouse model of Alzheimer's disease

机译:单核RNA测序显示阿尔茨海默病APP23小鼠模型中海马神经元的转录变化

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Alzheimer's disease (AD) is a progressive neurodegenerative disorder that mostly strikes the elderly. However, the exact molecular and cellular pathogenesis of AD, especially the dynamic changes of neurons during disease progression, remains poorly understood. Here we used single-nucleus RNA sequencing (snRNA-seq) to access the transcriptional changes of hippocampal neurons in APP23 mouse model of AD. We performed snRNA-seq using a modified Smart-seq2 technique on 3,280 neuronal nuclei from the hippocampus of young and aged APP23 and control mice and identified four distinct subpopulations. Comparative transcriptional analysis showed multiple changes in different subtypes of hippocampal neurons of APP23 mice in comparison to control mice, as well as the transcriptional changes in these neurons during disease progression. Our findings revealed multiple neuronal subtype-specific transcriptional changes that may lead to targets for future studies of AD.
机译:阿尔茨海默病(AD)是一种渐进神经退行性疾病,主要袭击老年人。 然而,AD的确切分子和细胞发病机制,特别是神经元在疾病进展期间的动态变化,仍然很差。 在这里,我们使用单核RNA测序(SNRNA-SEQ)来获得AP23小鼠模型中海马神经元的转录变化。 我们在杨和老年APP23海马的3,280个神经元核上使用修饰的智能SEQ2技术进行了SNRNA-SEQ,并鉴定了四个不同的群体。 比较转录分析表明,与对小鼠相比,APP23小鼠的海马神经元的不同亚型的多种变化,以及在疾病进展过程中这些神经元的转录变化。 我们的研究结果揭示了多种神经元亚型的转录变化,可能导致AD的未来研究的目标。

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