返老还童
神经科学
衰老的大脑
脑老化
细胞
神经干细胞
健康衰老
组学
脑功能
认知
干细胞
认知功能衰退
生物
心理学
计算生物学
生物信息学
医学
老年学
痴呆
细胞生物学
病理
疾病
遗传学
作者
Eric Sun,Rahul Nagvekar,Angela N. Pogson,Anne Brunet
出处
期刊:Neuron
[Elsevier]
日期:2025-01-01
卷期号:113 (1): 82-108
标识
DOI:10.1016/j.neuron.2024.12.007
摘要
SummaryBrain aging leads to a decline in cognitive function and a concomitant increase in the susceptibility to neurodegenerative diseases such as Alzheimer's and Parkinson's diseases. A key question is how changes within individual cells of the brain give rise to age-related dysfunction. Developments in single-cell "omics" technologies, such as single-cell transcriptomics, have facilitated high-dimensional profiling of individual cells. These technologies have led to new and comprehensive characterizations of brain aging at single-cell resolution. Here, we review insights gleaned from single-cell omics studies of brain aging, starting with a cell-type-centric overview of age-associated changes and followed by a discussion of cell-cell interactions during aging. We highlight how single-cell omics studies provide an unbiased view of different rejuvenation interventions and comment on the promise of combinatorial rejuvenation approaches for the brain. Finally, we propose new directions, including models of brain aging and neural stem cells as a focal point for rejuvenation.
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