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dc.creatorMartín López, Maríaes
dc.creatorGonzález Muñoz, Elenaes
dc.creatorGómez-González, Emilioes
dc.creatorSánchez Pernaute, Rosarioes
dc.creatorMárquez Rivas, Javieres
dc.creatorFernández Muñoz, Beatrizes
dc.date.accessioned2022-09-19T16:11:26Z
dc.date.available2022-09-19T16:11:26Z
dc.date.issued2021
dc.identifier.citationMartín López, M., González Muñoz, E., Gómez González, E., Sánchez Pernaute, R., Márquez Rivas, J. y Fernández Muñoz, B. (2021). Modeling chronic cervical spinal cord injury in aged rats for cell therapy studies. Journal of Clinical Neuroscience, 94, 76-85.
dc.identifier.issn0967-5868es
dc.identifier.urihttps://hdl.handle.net/11441/137212
dc.description.abstractWith an expanding elderly population, an increasing number of older adults will experience spinal cord injury (SCI) and might be candidates for cell-based therapies, yet there is a paucity of research in this age group. The objective of the present study was to analyze how aged rats tolerate behavioral testing, sur- gical procedures, post-operative complications, intra-spinal cell transplantation and immunosuppres- sion, and to examine the effectiveness of human iPSC-derived Neural Progenitor Cells (IMR90-hiPSC- NPCs) in a model of SCI. We performed behavioral tests in rats before and after inducing cervical hemi-contusions at C4 level with a fourth-generation Ohio State University Injury Device. Four weeks later, we injected IMR90-hiPSC-NPCs in animals that were immunosuppressed by daily cyclosporine injection. Four weeks after injection we analyzed locomotor behavior and mortality, and histologically assessed the survival of transplanted human NPCs. As rats aged, their success at completing behavioral tests decreased. In addition, we observed high mortality rates during behavioral training (41.2%), after cervical injury (63.2%) and after cell injection (50%). Histological analysis revealed that injected cells sur- vived and remained at and around the grafted site and did not cause tumors. No locomotor improvement was observed in animals four weeks after IMR90-hiPSC-NPC transplantation. Our results show that elderly rats are highly vulnerable to interventions, and thus large groups of animals must be initially established to study the potential efficacy of cell-based therapies in age-related chronic myelopathies.es
dc.description.sponsorshipConsejería de Transformación Económica, Industria, Conocimiento y Universidades de la Junta de Andalucía RyC 2014-15410es
dc.formatapplication/pdfes
dc.format.extent10 p.es
dc.language.isoenges
dc.publisherChurchill Livingstonees
dc.relation.ispartofJournal of Clinical Neuroscience, 94, 76-85.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectSCIes
dc.subjectMyelopathyes
dc.subjectPluripotent stem cellses
dc.subjectiPSCses
dc.subjectNPCses
dc.subjectElderlyes
dc.subjectAdvanced therapieses
dc.titleModeling chronic cervical spinal cord injury in aged rats for cell therapy studieses
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Física Aplicada IIIes
dc.relation.projectIDRyC 2014-15410es
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0967586821004987es
dc.identifier.doi10.1016/j.jocn.2021.09.042es
dc.contributor.groupUniversidad de Sevilla. TEP-203: Física Interdisciplinar Fundamentos y aplicacioneses
dc.journaltitleJournal of Clinical Neurosciencees
dc.publication.volumen94es
dc.publication.initialPage76es
dc.publication.endPage85es
dc.contributor.funderConsejería de Salud y Familias de Andalucía a la Red Andaluza de Diseño y Traslación de Terapias Avanzadas y fondos privados.es

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