小胶质细胞
疾病
计算生物学
神经科学
核糖核酸
电池类型
阿尔茨海默病
生物
细胞
生物信息学
遗传学
医学
基因
病理
免疫学
炎症
作者
Wengang Jin,Jinjin Pei,Jeane Rebecca Roy,Selvaraj Jayaraman,Rathi Muthaiyan Ahalliya,Velliyur Kanniappan Gopalakrishnan,Monica Mironescu,Chella Perumal Palanisamy
标识
DOI:10.1016/j.arr.2024.102454
摘要
Alzheimer's disease (AD) is a multifaceted neurodegenerative condition marked by gradual cognitive deterioration and the loss of neurons. While conventional bulk RNA sequencing techniques have shed light on AD pathology, they frequently obscure the cellular diversity within brain tissues. The advent of single-cell RNA sequencing (scRNA-seq) has transformed our capability to analyze the cellular composition of AD, allowing for the detection of unique cell populations, rare cell types, and gene expression alterations at an individual cell level. This review examines the use of scRNA-seq in AD research, focusing on its contributions to understanding cellular diversity, disease progression, and potential therapeutic targets. We discuss key technological innovations, data analysis techniques, and challenges associated with scRNA-seq in studying AD. Furthermore, we highlight recent studies that have utilized scRNA-seq to identify novel biomarkers, uncover disease-associated pathways, and elucidate the role of non-neuronal cells, such as microglia and astrocytes, in AD pathogenesis. By providing a comprehensive overview of advancements in scRNA-seq for unraveling cellular heterogeneity in AD, this review highlights the transformative impact of scRNA-seq on our comprehension of disease mechanisms and the creation of targeted treatments.
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