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dc.contributor.authorPérez Montes, Cristina
dc.contributor.authorHernández García, Rosalía
dc.contributor.authorJiménez Cubides, Jhoana Paola
dc.contributor.authorOliveira Mello, Laura de
dc.contributor.authorVelasco Arranz, María Almudena 
dc.contributor.authorArévalo Arévalo, María Rosario 
dc.contributor.authorGarcía Macia, Marina 
dc.contributor.authorSantos Ledo, Adrián 
dc.date.accessioned2026-07-15T10:22:41Z
dc.date.available2026-07-15T10:22:41Z
dc.date.issued2024-10-22
dc.identifier.issn1673-5374
dc.identifier.urihttp://hdl.handle.net/10366/172187
dc.description.abstract[EN] The visual system of teleost fish grows continuously, which is a useful model for studying regeneration of the central nervous system. Glial cells are key for this process, but their contribution is still not well defined. We followed oligodendrocytes in the visual system of adult zebrafish during regeneration of the optic nerve at 6, 24, and 72 hours post-lesion and at 7 and 14 days post-lesion via the sox10:tagRFP transgenic line and confocal microscopy. To understand the changes that these oligodendrocytes undergo during regeneration, we used Sox2 immunohistochemistry, a stem cell marker involved in oligodendrocyte differentiation. We also used the Click-iT™ Plus TUNEL assay to study cell death and a BrdU assay to determine cell proliferation. Before optic nerve crush, sox10:tagRFP oligodendrocytes are located in the retina, in the optic nerve head, and through all the entire optic nerve. Sox2-positive cells are present in the peripheral germinal zone, the mature retina, and the optic nerve. After optic nerve crush, sox10:tagRFP cells disappeared from the optic nerve crush zone, suggesting that they died, although they were not TUNEL positive. Concomitantly, the number of Sox2-positive cells increased around the crushed area, the optic nerve head, and the retina. Then, between 24 hours post-lesion and 14 days post-lesion, double sox10:tagRFP/Sox2-positive cells were detected in the retina, optic nerve head, and whole optic nerve, together with a proliferation response at 72 hours post-lesion. Our results confirm that a degenerating process may occur prior to regeneration. First, sox10:tagRFP oligodendrocytes that surround the degenerated axons stop wrapping them, change their “myelinating oligodendrocyte” morphology to a “nonmyelinating oligodendrocyte” morphology, and die. Then, residual oligodendrocyte progenitor cells in the optic nerve and retina proliferate and differentiate for the purpose of remyelination. As new axons arise from the surviving retinal ganglion cells, new sox10:tagRFP oligodendrocytes arise from residual oligodendrocyte progenitor cells to guide, nourish and myelinate them. Thus, oligodendrocytes play an active role in zebrafish axon regeneration and remyelination.es_ES
dc.description.sponsorshipThis study was supported by the Lanzadera TCUE and C2 program (Universidad de Salamanca) (to ASL); the Spanish National Research Council (CSIC) funded by the Junta de Castilla y León and co-financed by the European Regional Development Fund (ERDF “Europe drives our growth)”: Internationalization Project “CL-EI-2021-08-IBFG Unit of Excellence”, Grant (PID2022-138478OA-100) funded by MICIU/AEI/10.13039/501100011033 and, by FEDER, UE (to MGM); Junta de Castilla y León (SA225P23) and Gerencia Regional de Salud (2701/A1/2023) (to AV); and the Plan Especial Grado Medicina (USAL) (to CPM). MGM is a Ramón y Cajal researcher: Grant RYC2021033684-I funded by MICIU/AEI/10.13039/501100011033 and, by European Union NextGenerationEU/PRTR.es_ES
dc.format.mimetypeapplicatio/pdf
dc.language.isoenges_ES
dc.rightsAtribución-NoComercial-CompartirIgual 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subjectCell deathes_ES
dc.subjectOligodendrocyteses_ES
dc.subjectOptic nervees_ES
dc.subjectProliferationes_ES
dc.subjectRegenerationes_ES
dc.subjectSox10es_ES
dc.subjectSox2es_ES
dc.subjectVisual systemes_ES
dc.subjectZebrafishes_ES
dc.titleZebrafish optic nerve regeneration involves resident and retinal oligodendrocyteses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.4103/nrr.nrr-d-24-00621
dc.subject.unesco2411.15 Fisiología de la Visión
dc.subject.unesco3207.11 Neuropatología
dc.identifier.doi10.4103/NRR.NRR-D-24-00621
dc.relation.projectIDCL-EI-2021-08-IBFGes_ES
dc.relation.projectIDPID2022-138478OA-100es_ES
dc.relation.projectIDMICIU/AEI/10.13039/501100011033es_ES
dc.relation.projectIDSA225P23es_ES
dc.relation.projectID2701/A1/2023es_ES
dc.relation.projectIDRYC2021033684-Ies_ES
dc.relation.projectIDMICIU/AEI/10.13039/501100011033es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1876-7958
dc.journal.titleNeural Regeneration Researches_ES
dc.volume.number21es_ES
dc.issue.number2es_ES
dc.page.initial811es_ES
dc.page.final820es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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