Institute on Aging and Brain Disorders, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Hefei National Laboratory for Physical Sciences at the Microscale, Neurodegenerative Disorder Research Center, School of Life Sciences, University of Science and Technology of China, Hefei, China.
Biosci Biotechnol Biochem. 2020 May;84(5):919-926. doi: 10.1080/09168451.2020.1714420. Epub 2020 Jan 13.
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.
阿尔茨海默病(AD)是一种渐进性神经退行性疾病,主要影响老年人。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过程中的动态变化,仍知之甚少。在这里,我们使用单核 RNA 测序(snRNA-seq)来研究 APP23 型 AD 小鼠模型中海马神经元的转录变化。我们使用改良的 Smart-seq2 技术对来自年轻和老年 APP23 型和对照小鼠海马体的 3280 个神经元核进行了 snRNA-seq,并鉴定出了四个不同的亚群。比较转录分析显示,与对照小鼠相比,APP23 小鼠的海马神经元的不同亚型发生了多种变化,以及这些神经元在疾病进展过程中的转录变化。我们的研究结果揭示了多种神经元亚型特异性的转录变化,这些变化可能为 AD 的未来研究提供潜在的靶点。