Single-nucleus RNA sequencing reveals glial cell type-specific responses to ischemic stroke in male rodents.
Animals
Ischemic Stroke
/ genetics
Male
Mice
Single-Cell Analysis
/ methods
Oligodendroglia
/ metabolism
Oligodendrocyte Precursor Cells
/ metabolism
Astrocytes
/ metabolism
Neuroglia
/ metabolism
Osteopontin
/ genetics
Transcriptome
Sequence Analysis, RNA
/ methods
Mice, Inbred C57BL
Brain
/ metabolism
Rats
Cell Proliferation
Cell Movement
/ genetics
Myeloid Cells
/ metabolism
Disease Models, Animal
Cell Nucleus
/ metabolism
Brain Ischemia
/ genetics
Journal
Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555
Informations de publication
Date de publication:
24 Jul 2024
24 Jul 2024
Historique:
received:
08
01
2024
accepted:
09
07
2024
medline:
24
7
2024
pubmed:
24
7
2024
entrez:
23
7
2024
Statut:
epublish
Résumé
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
Identifiants
pubmed: 39043661
doi: 10.1038/s41467-024-50465-z
pii: 10.1038/s41467-024-50465-z
doi:
Substances chimiques
Osteopontin
106441-73-0
Spp1 protein, mouse
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
6232Subventions
Organisme : Österreichische Forschungsförderungsgesellschaft (Austrian Research Promotion Agency)
ID : #898252
Organisme : Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.)
ID : #1R01NS114227-01A1
Organisme : Austrian Science Fund (Fonds zur Förderung der Wissenschaftlichen Forschung)
ID : #T109, #P31085-B26
Informations de copyright
© 2024. The Author(s).
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