Utilize este identificador para referenciar este registo: https://hdl.handle.net/10216/159419
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Campo DCValorIdioma
dc.creatorBielefeld, P-
dc.creatorMartirosyan, A-
dc.creatorMartín-Suárez, S-
dc.creatorApresyan, A-
dc.creatorMeerhoff, GF-
dc.creatorPestana, F-
dc.creatorPoovathingal, S-
dc.creatorReijner, N-
dc.creatorKoning, W-
dc.creatorClement, RA-
dc.creatorVeen, IVd-
dc.creatorToledo, EM-
dc.creatorPolzer, O-
dc.creatorDurá, I-
dc.creatorHovhannisyan, S-
dc.creatorNilges, BS-
dc.creatorBogdoll, A-
dc.creatorKashikar, ND-
dc.creatorLucassen, PJ-
dc.creatorBelgard, TG-
dc.creatorEncinas, JM-
dc.creatorHolt, MG-
dc.creatorFitzsimons, CP-
dc.date.accessioned2024-07-10T17:17:27Z-
dc.date.available2024-07-10T17:17:27Z-
dc.date.issued2024-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://hdl.handle.net/10216/159419-
dc.description.abstractTraumatic 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.pt_PT
dc.description.sponsorshipP.B., G.M., N.R., W.K., R.A.C., I.v.d.V., E.T., I.D., S.M.-S., O.P., J.M.E., and C.P.F. were supported by the European Union’s Horizon 2020 research and innovation program ERA-NET-NEURON (grant EJTC 2016) to C.P.F. and J.M.E., by the Netherlands Organization for Scientific research (NWO, cofund ERA-NET-NEURON EJTC 2016 to C.P.F.), and by Alzheimer Nederland (grant WE03202007 to C.P.F.). JME acknowledges funding from La Caixa Foundation R23-00860; MICINN with FEDER Funds PCIN-2016-128 and PID2019-104766RB; MICINN CPP2022009779 and Basque Government PIBA_2021_1_0018. S.M.-S. acknowledges funding from MICINN RYC-2021-033215-I and Basque Government PIBA_2023_1_0045. P.J.L. is supported by the Center for Urban Mental Health, University of Amsterdam, The Netherlands, and by Alzheimer Nederland. MGH’s work in Leuven was supported by the Belgian Scientific Research Fund (Fonds Wetenschappelijk Onderzoek —FWO—Grants G066715N, 1523014N, and I001818N) and the Belgian Alzheimer’s Society (SAO) (Grant S#16025). MGH is currently the ERA Chair (NCBio) at i3S Porto, funded by the European Commission (H2020-WIDESPREAD-2018-2020-6; NCBio; 951923). A.M. acknowledges funding from the Stichting Alzheimer Onderzoek (SAO #2020034) and VIB Tec Watch funding. F.P. was supported by a Fundação para a Ciência e a Tecnologia (FCT) Ph.D. fellowship (2020.08750.BD). The authors acknowledge the help and advice of Dr. Dirk-Jan Saaltink in the graphic design and preparation of the cell schemes in Figs. 1o and 5g, Scheme in Fig. 5g is used with his author’s permission. The RV-GFP vector was kindly provided by Kristoffer Riecken at the Medical Center Hamburg-Eppendorf (UKE), Germany. We gratefully acknowledge the use and support of the confocal microscopes at The van Leeuwenhoek Centre for Advanced Microscopy, Section of Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam.pt_PT
dc.language.isoengpt_PT
dc.publisherNature Pub. Grouppt_PT
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/951923/EU-
dc.relation.ispartofseriesNature communications, vol. 15(1):5222pt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.meshAnimals-
dc.subject.meshAstrocytes/metabolism-
dc.subject.meshBrain Injuries, Traumatic / pathology-
dc.subject.meshBrain Injuries, Traumatic / physiopathology-
dc.subject.meshCell Differentiation-
dc.subject.meshDentate Gyrus / pathology-
dc.subject.meshDisease Models, Animal-
dc.subject.meshHippocampus / cytology-
dc.subject.meshHippocampus / pathology-
dc.subject.meshMale-
dc.subject.meshMice-
dc.subject.meshMice, Inbred C57BL-
dc.subject.meshNeural Stem Cells / cytology-
dc.subject.meshNeural Stem Cells / metabolism-
dc.subject.meshNeurogenesis-
dc.subject.meshNeurons / metabolism-
dc.subject.meshTranscriptome-
dc.titleTraumatic brain injury promotes neurogenesis at the cost of astrogliogenesis in the adult hippocampus of male micept_PT
dc.typeArtigo em Revista Científica Internacionalpt_PT
dc.contributor.uportoInstituto de Investigação e Inovação em Saúdept_PT
dc.identifier.doi10.1038/s41467-024-49299-6-
dc.relation.publisherversionhttps://www.nature.com/articles/s41467-024-49299-6-
Aparece nas coleções:I3S - Artigo em Revista Científica Internacional

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