生物
自噬
ATG5型
基因
转录组
核糖核酸
细胞
基因表达
细胞生物学
遗传学
细胞凋亡
作者
Chuanbin Yang,Siyu Xia,Wei Zhang,Han‐Ming Shen,Jigang Wang
出处
期刊:Autophagy
[Taylor & Francis]
日期:2022-06-23
卷期号:19 (2): 706-715
被引量:10
标识
DOI:10.1080/15548627.2022.2091903
摘要
Dysregulation of macroautophagy/autophagy has been closely implicated in aging. Caloric restriction (CR) is an effective intervention of aging partially via activation of autophagy. Recently, a high-throughput single-cell RNA-seq technique has been employed to detect the comprehensive transcriptomes of individual cells. However, the transcriptional networks of ATG (autophagy related) genes in the aging process and the modulation of ATG genes expression by CR at the single-cell level have not been elucidated. Here, by performing data analysis of single nucleus/cells RNA sequencing in rats undergoing aging and the modulation by CR, we demonstrate that the transcription patterns of Atg genes in different cell types of rat liver, brain, and kidney are highly heterogeneous. Importantly, CR reversed aging-induced changes of multiple Atg genes across different cell types in the brain, liver, and kidney. In summary, our results, for the first time, provide comprehensive information on Atg gene expression in specific cell types of different organs in a mammal during aging and give novel insight into the protective role of autophagy and CR in aging at the single-cell resolution.
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