Yu Gefei, Thorpe Abigail, Zeng Qi, Wang Erming, Cai Dongming, Wang Minghui, Zhang Bin
bioRxiv. 2024 Dec 5:2024.12.01.626234. doi: 10.1101/2024.12.01.626234.
Alzheimer's disease (AD) is the most common form of dementia, with approximately two-thirds of AD patients are females. Basic and clinical research studies show evidence supporting sex-specific differences contributing to the complexity of AD. There is also strong evidence supporting sex-specific interaction between the primary genetic risk factor of AD, and AD-associated neurodegenerative processes. Recent studies by us and others have identified sex and/or APOE4 specific differentially expressed genes in AD based on the bulk tissue RNA-sequencing data of postmortem human brain samples in AD. However, there lacks a comprehensive investigation of the interplay between sex and APOE genotypes at the single cell level. In the current study, we systematically explore sex and APOE genotype differences in single cell transcriptomics in AD. Our work provides a comprehensive overview of sex and APOE genotype-specific transcriptomic changes across 54 high-resolution cell types in AD and highlights individual genes and brain cell types that show significant differences between sexes and APOE genotypes. This study lays the groundwork for exploring the complex molecular mechanisms of AD and will inform the development of effective sex- and APOE-stratified interventions for AD.
阿尔茨海默病(AD)是最常见的痴呆形式,约三分之二的AD患者为女性。基础和临床研究表明,有证据支持性别特异性差异导致了AD的复杂性。也有强有力的证据支持AD的主要遗传风险因素与AD相关神经退行性过程之间的性别特异性相互作用。我们和其他人最近的研究基于AD患者死后人类大脑样本的大量组织RNA测序数据,确定了AD中性别和/或APOE4特异性差异表达基因。然而,在单细胞水平上,缺乏对性别与APOE基因型之间相互作用的全面研究。在当前的研究中,我们系统地探索了AD单细胞转录组学中的性别和APOE基因型差异。我们的工作全面概述了AD中54种高分辨率细胞类型的性别和APOE基因型特异性转录组变化,并突出显示了在性别和APOE基因型之间存在显著差异的个别基因和脑细胞类型。这项研究为探索AD的复杂分子机制奠定了基础,并将为AD有效的性别和APOE分层干预措施的开发提供信息。