Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/159419
Author(s): Bielefeld, P
Martirosyan, A
Martín-Suárez, S
Apresyan, A
Meerhoff, GF
Pestana, F
Poovathingal, S
Reijner, N
Koning, W
Clement, RA
Veen, IVd
Toledo, EM
Polzer, O
Durá, I
Hovhannisyan, S
Nilges, BS
Bogdoll, A
Kashikar, ND
Lucassen, PJ
Belgard, TG
Encinas, JM
Holt, MG
Fitzsimons, CP
Title: Traumatic brain injury promotes neurogenesis at the cost of astrogliogenesis in the adult hippocampus of male mice
Publisher: Nature Pub. Group
Issue Date: 2024
Abstract: Traumatic brain injury (TBI) can result in long-lasting changes in hippocampal function. The changes induced by TBI on the hippocampus contribute to cognitive deficits. The adult hippocampus harbors neural stem cells (NSCs) that generate neurons (neurogenesis), and astrocytes (astrogliogenesis). While deregulation of hippocampal NSCs and neurogenesis have been observed after TBI, it is not known how TBI may affect hippocampal astrogliogenesis. Using a controlled cortical impact model of TBI in male mice, single cell RNA sequencing and spatial transcriptomics, we assessed how TBI affected hippocampal NSCs and the neuronal and astroglial lineages derived from them. We observe an increase in NSC-derived neuronal cells and a concomitant decrease in NSC-derived astrocytic cells, together with changes in gene expression and cell dysplasia within the dentate gyrus. Here, we show that TBI modifies NSC fate to promote neurogenesis at the cost of astrogliogenesis and identify specific cell populations as possible targets to counteract TBI-induced cellular changes in the adult hippocampus.
DOI: 10.1038/s41467-024-49299-6
URI: https://hdl.handle.net/10216/159419
Series: Nature communications, vol. 15(1):5222
Related Information: info:eu-repo/grantAgreement/EC/H2020/951923/EU
Document Type: Artigo em Revista Científica Internacional
Rights: openAccess
License: https://creativecommons.org/licenses/by/4.0/
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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