Neuroscience Institute, NYU Grossman School of Medicine, New York, NY 10016, USA.
Center for Cognitive Neurology, NYU Grossman School of Medicine, New York, NY 10016, USA; Department of Pathology, NYU Langone Health, New York, NY 10016, USA.
Neuron. 2022 Jun 1;110(11):1788-1805.e10. doi: 10.1016/j.neuron.2022.03.008. Epub 2022 Apr 4.
Resolving glial contributions to Alzheimer's disease (AD) is necessary because changes in neuronal function, such as reduced synaptic density, altered electrophysiological properties, and degeneration, are not entirely cell autonomous. To improve understanding of transcriptomic heterogeneity in glia during AD, we used single-nuclei RNA sequencing (snRNA-seq) to characterize astrocytes and oligodendrocytes from apolipoprotein (APOE) Ɛ2/3 human AD and age- and genotype-matched non-symptomatic (NS) brains. We enriched astrocytes before sequencing and characterized pathology from the same location as the sequenced material. We characterized baseline heterogeneity in both astrocytes and oligodendrocytes and identified global and subtype-specific transcriptomic changes between AD and NS astrocytes and oligodendrocytes. We also took advantage of recent human and mouse spatial transcriptomics resources to localize heterogeneous astrocyte subtypes to specific regions in the healthy and inflamed brain. Finally, we integrated our data with published AD snRNA-seq datasets, highlighting the power of combining datasets to resolve previously unidentifiable astrocyte subpopulations.
解析神经胶质细胞对阿尔茨海默病(AD)的作用是必要的,因为神经元功能的改变,如突触密度降低、电生理特性改变和退化,并不完全是细胞自主的。为了更好地理解 AD 期间神经胶质细胞的转录组异质性,我们使用单核 RNA 测序(snRNA-seq)来描述载脂蛋白(APOE) Ɛ2/3 人类 AD 和年龄及基因型匹配的无症状(NS)大脑中的星形胶质细胞和少突胶质细胞。我们在测序前富集星形胶质细胞,并从与测序材料相同的位置描述病理学。我们描述了星形胶质细胞和少突胶质细胞的基线异质性,并确定了 AD 和 NS 星形胶质细胞和少突胶质细胞之间的整体和亚型特异性转录组变化。我们还利用最近的人类和小鼠空间转录组学资源将异质星形胶质细胞亚型定位到健康和炎症大脑的特定区域。最后,我们将我们的数据与已发表的 AD snRNA-seq 数据集进行整合,突出了结合数据集来解析以前无法识别的星形胶质细胞亚群的优势。