Decoding the Transcriptional Response to Ischemic Stroke in Young and Aged Mouse Brain
Peter Androvic,
Denisa Kirdajova,
Jana Tureckova,
Daniel Zucha,
Eva Rohlova,
Pavel Abaffy,
Jan Kriska,
Martin Valny,
Miroslava Anderova,
Mikael Kubista,
Lukas Valihrach
Affiliations
Peter Androvic
Institute of Biotechnology of the Czech Academy of Sciences–BIOCEV, Vestec, Czech Republic; Laboratory of Growth Regulators, Faculty of Science, Palacky University, Olomouc, Czech Republic; Corresponding author
Denisa Kirdajova
Institute of Experimental Medicine of the Czech Academy of Sciences, Prague, Czech Republic; Second Medical Faculty, Charles University, Prague, Czech Republic
Jana Tureckova
Institute of Experimental Medicine of the Czech Academy of Sciences, Prague, Czech Republic
Daniel Zucha
Institute of Biotechnology of the Czech Academy of Sciences–BIOCEV, Vestec, Czech Republic
Eva Rohlova
Institute of Biotechnology of the Czech Academy of Sciences–BIOCEV, Vestec, Czech Republic
Pavel Abaffy
Institute of Biotechnology of the Czech Academy of Sciences–BIOCEV, Vestec, Czech Republic
Jan Kriska
Institute of Experimental Medicine of the Czech Academy of Sciences, Prague, Czech Republic; Second Medical Faculty, Charles University, Prague, Czech Republic
Martin Valny
Institute of Experimental Medicine of the Czech Academy of Sciences, Prague, Czech Republic
Miroslava Anderova
Institute of Experimental Medicine of the Czech Academy of Sciences, Prague, Czech Republic
Mikael Kubista
Institute of Biotechnology of the Czech Academy of Sciences–BIOCEV, Vestec, Czech Republic
Lukas Valihrach
Institute of Biotechnology of the Czech Academy of Sciences–BIOCEV, Vestec, Czech Republic; Corresponding author
Summary: 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.