Li, XuanLyu, JingjunLi, RanJain, VaibhavShen, YuntianDel Águila, ÁngelaHoffmann, UlrikeSheng, HuaxinYang, Wei2022-04-212022-04-212022-04-071742-20941742-2094https://hdl.handle.net/10161/24851<h4>Background</h4>Ischemic stroke is a medical emergency that primarily affects the elderly. A complex immune response in the post-stroke brain constitutes a key component of stroke pathophysiology. This study aimed to determine how stroke affects immune cell populations in the aged brain based on molecular profiles of individual cells.<h4>Methods</h4>Single-cell RNA sequencing and a new transient ischemic stroke mouse model with late reperfusion were used.<h4>Results</h4>We generated, for the first time, a composite picture of immune cell populations in the stroke aged brain at single-cell resolution. We discovered at least 6 microglial subsets in the stroke aged brain, including a potentially stroke-specific subtype. Moreover, we identified major cell subpopulations formed by infiltrated myeloid cells after stroke, and revealed their unique molecular profiles.<h4>Conclusions</h4>This study provided the first scRNA-seq data set for immune cells in the stroke aged brain, and offered novel insights into post-stroke immune cell heterogeneity.BrainMicrogliaAnimalsMiceStrokeSingle-Cell AnalysisTranscriptomeIschemic StrokeJournal article2022-04-21