生物
骨桥蛋白
少突胶质细胞
小胶质细胞
转录组
表型
电池类型
神经科学
星形胶质细胞
CD44细胞
室下区
神经胶质
细胞生物学
细胞
病理
炎症
免疫学
医学
干细胞
中枢神经系统
神经干细胞
基因表达
基因
遗传学
髓鞘
作者
Daniel Bormann,Michael Knoflach,Emilia Poreba,Christian J. Riedl,Giulia Testa,Cyrille Orset,Anthony Levilly,Andreá Cottereau,Philipp Jauk,Simon Hametner,Nadine Stranzl,Bahar Golabi,Dragan Copic,Katharina Klas,Martin Direder,Hannes Kühtreiber,Melanie Salek,Stephanie zur Nedden,Gabriele Baier‐Bitterlich,Stefan Kiechl
标识
DOI:10.1038/s41467-024-50465-z
摘要
Neuroglia critically shape the brain´s response to ischemic stroke. However, their phenotypic heterogeneity impedes a holistic understanding of the cellular composition of the early ischemic lesion. Here we present a single cell resolution transcriptomics dataset of the brain´s acute response to infarction. Oligodendrocyte lineage cells and astrocytes range among the most transcriptionally perturbed populations and exhibit infarction- and subtype-specific molecular signatures. Specifically, we find infarction restricted proliferating oligodendrocyte precursor cells (OPCs), mature oligodendrocytes and reactive astrocytes, exhibiting transcriptional commonalities in response to ischemic injury. OPCs and reactive astrocytes are involved in a shared immuno-glial cross talk with stroke-specific myeloid cells. Within the perilesional zone, osteopontin positive myeloid cells accumulate in close proximity to CD44
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