Comparison of Different in Vitro Models of Alzheimer's Disease Using Re-Analysis of Scrna-Seq Data

Yu-Ra Kang
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引用次数: 1

Abstract

Alzheimer's disease (AD) is a neurodegenerative disease affecting at least 35 million people worldwide, creating significant health and social care challenges. In this research, I aim to investigate the molecular pathways contributing to AD pathology by using publicly available datasets generated from different in vitro models of Alzheimer's disease. To address this aim, I re-analyzed single-cell RNA-Seq datasets derived from Cakir, B. et al (2022, GSE175719) and Pérez, J.J. et al. (2020, GSE147047). Using the Seurat package in RStudio, I compared gene expression of cortical neurons from dementia groups, modelled with PITRM1 knockout or addition of amyloid-beta into the cultures, to that of untreated neurons. Combination of single-cell RNA-Seq allowing single-cell resolution with different in vitro models of Alzheimer's disease might help to elucidate the pathways involved in Alzheimer's disease pathology.
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利用Scrna-Seq数据重新分析不同阿尔茨海默病体外模型的比较
阿尔茨海默病(AD)是一种影响全球至少3500万人的神经退行性疾病,给健康和社会保健带来了重大挑战。在这项研究中,我的目的是通过使用从不同的阿尔茨海默病体外模型生成的公开可用数据集来研究促进AD病理的分子途径。为了解决这一问题,我重新分析了Cakir, B.等人(2022,GSE175719)和p rez, J.J.等人(2020,GSE147047)的单细胞RNA-Seq数据集。使用RStudio中的Seurat包,我比较了痴呆症组皮质神经元的基因表达,通过敲除PITRM1或在培养物中添加淀粉样蛋白来模拟,与未处理的神经元。单细胞RNA-Seq的结合允许单细胞分辨率与不同的阿尔茨海默病的体外模型可能有助于阐明阿尔茨海默病的病理通路。
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