| Literature DB >> 32553170 |
Peter Androvic1, Denisa Kirdajova2, Jana Tureckova3, Daniel Zucha4, Eva Rohlova4, Pavel Abaffy4, Jan Kriska2, Martin Valny3, Miroslava Anderova3, Mikael Kubista4, Lukas Valihrach5.
Abstract
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.Entities:
Keywords: RNA-seq; WGCNA; aging; axon; cerebral ischemia; gene expression; interferon; parvalbumin; stroke; synapse
Mesh:
Year: 2020 PMID: 32553170 DOI: 10.1016/j.celrep.2020.107777
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423