Modeling chronic cervical spinal cord injury in aged rats for cell therapy studies.

dc.centroFacultad de Cienciases_ES
dc.contributor.authorMartín-López, Maria
dc.contributor.authorGonzález-Muñoz, María Elena
dc.contributor.authorGómez González, Emilio
dc.contributor.authorSánchez Pernaute, Rosario
dc.contributor.authorMárquez-Rivas, Javier
dc.contributor.authorFernández-Muñoz, Beatriz
dc.date.accessioned2025-06-03T11:02:47Z
dc.date.available2025-06-03T11:02:47Z
dc.date.issued2021-09-30
dc.departamentoBiología Celular, Genética y Fisiologíaes_ES
dc.departamentoBIONAND. Centro Andaluz de Nanomedicina y Biotecnologíaes_ES
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, surgical procedures, post-operative complications, intra-spinal cell transplantation and immunosuppression, 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 survived 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_ES
dc.identifier.citationModeling chronic cervical spinal cord injury in aged rats for cell therapy studies Martín-López, María et al. Journal of Clinical Neuroscience, Volume 94, 76 - 85es_ES
dc.identifier.doi10.1016/j.jocn.2021.09.042
dc.identifier.urihttps://hdl.handle.net/10630/38817
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relation.projectIDRyC 2014-15410es_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectColumna vertebral - Lesiones y heridases_ES
dc.subjectAncianoses_ES
dc.subjectCélulas madrees_ES
dc.subjectTerapia celulares_ES
dc.subject.otherSCIes_ES
dc.subject.otherMyelopathyes_ES
dc.subject.otherPluripotent stem cellses_ES
dc.subject.otheriPSCses_ES
dc.subject.otherNPCses_ES
dc.subject.otherElderlyes_ES
dc.subject.otherAdvanced therapieses_ES
dc.titleModeling chronic cervical spinal cord injury in aged rats for cell therapy studies.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicationfb92caee-eee5-41f6-9e58-601d4ea47b65
relation.isAuthorOfPublication.latestForDiscoveryfb92caee-eee5-41f6-9e58-601d4ea47b65

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