冲程(发动机)
疾病
下调和上调
基因表达
基因
神经科学
生物信息学
缺血性中风
衰老
医学
生物
内科学
缺血
遗传学
机械工程
工程类
作者
Peter Androvic,Denisa Kirdajová,Jana Turečková,Daniel Žucha,Eva Rohlova,Pavel Abaffy,Ján Kriška,Martin Valný,Miroslava Andĕrová,Mikael Kubista,Lukás Valihrach
出处
期刊:Cell Reports
[Cell Press]
日期:2020-06-01
卷期号:31 (11): 107777-107777
被引量:89
标识
DOI:10.1016/j.celrep.2020.107777
摘要
Ischemic stroke is a well-recognized disease of aging, yet it is unclear how the age-dependent vulnerability occurs and what are the underlying mechanisms. To address these issues, we perform a comprehensive RNA-seq analysis of aging, ischemic stroke, and their interaction in 3- and 18-month-old mice. We assess differential gene expression across injury status and age, estimate cell type proportion changes, assay the results against a range of transcriptional signatures from the literature, and perform unsupervised co-expression analysis, identifying modules of genes with varying response to injury. We uncover downregulation of axonal and synaptic maintenance genetic program, and increased activation of type I interferon (IFN-I) signaling following stroke in aged mice. Together, these results paint a picture of ischemic stroke as a complex age-related disease and provide insights into interaction of aging and stroke on cellular and molecular level.
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