Cell Reports · 2020 · 117 citations · 137 references
Life SciencesMolecular BiologyNeuroscienceGene ExpressionMolecular NeuroscienceTranscriptomicsAcute Ischemic StrokeBiological AgingInflammatory SignalingInterferon ResponsesNeuroinflammationStrokeCell-type Proportion EstimationDifferential Co-expression AnalysisDifferential Gene ExpressionDifferential Transcript ExpressionInjury-induced Gene ExpressionIschemic Stroke PathologyIschemic Stroke PathophysiologySynaptic Maintenance
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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