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dc.contributor.authorDíaz López, David 
dc.contributor.authorSánchez Recio, Javier
dc.contributor.authorWeruaga Prieto, Eduardo 
dc.contributor.authorAlonso Peña, José Ramón 
dc.date.accessioned2026-01-15T13:52:57Z
dc.date.available2026-01-15T13:52:57Z
dc.date.issued2012
dc.identifier.citationDíaz, D., Recio, J. S., Weruaga, E., y Alonso, J. R. (2012). Mild cerebellar neurodegeneration of aged heterozygous pcd mice increases cell fusion of purkinje and bone marrow-derived cells. Cell Transplantation, 21(7), 1595-1602. https://doi.org/10.3727/096368912X638900es_ES
dc.identifier.issn0963-6897
dc.identifier.urihttp://hdl.handle.net/10366/168842
dc.description.abstract[EN] Bone marrow-derived cells have different plastic properties, especially regarding cell fusion, which increases with time and is prompted by tissue injury. Several recessive mutations, including Purkinje Cell Degeneration, affect the number of Purkinje cells in homozygosis; heterozygous young animals have an apparently normal phenotype but they undergo Purkinje cell loss as they age. Our findings demonstrate that heterozygous pcd mice undergo Purkinje cell loss at postnatal day 300, this slow but steadily progressing cell death starting sooner than has been reported previously and without massive reactive gliosis or inflammation. Here, transplantation of bone marrow stem cells was performed to assess the arrival of bone marrow-derived cells in the cerebellum in these heterozygous mice. Our results reveal that a higher number of cell fusion events occurs in heterozygous animals than in the controls, on days 150 and 300 postnatally. In sum, this study indicates that mild cell death promotes the fusion of bone marrow-derived cells with surviving Purkinje neurons. This phenomenon suggests new therapies for long-lasting neurodegenerative disorders.es_ES
dc.description.sponsorshipThis work was supported by the Ministerio de Investigación y Ciencia (BFU2010-18284), the Ministerio de Sanidad, Política Social e Igualdad (Plan Nacional Sobre Drogas), the Junta de Castilla y León, the Centre for Regenerative Medicine and Cell Therapy of Castilla y León, the Fundación Samuel Solórzano, and the University of Salamanca. The authors also express their gratitude to N. Skinner and C. Bruggeman for revising the English version of the manuscript. The authors declare no conflicts of interest.es_ES
dc.format.mimetypeapplicatio/pdf
dc.language.isoenges_ES
dc.publisherSAGE Publicationses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCell fusiones_ES
dc.subjectCerebellumes_ES
dc.subjectNeurorepaires_ES
dc.subjectPurkinje cell degenerationes_ES
dc.subjectPurkinje cellses_ES
dc.subjectTransplantes_ES
dc.subject.meshBone Marrow Cells *
dc.subject.meshNerve Degeneration *
dc.subject.meshPurkinje Cells *
dc.subject.meshStem Cell Transplantation *
dc.subject.meshCell Fusion *
dc.subject.meshAnimals *
dc.subject.meshNeurodegenerative Diseases *
dc.subject.meshCerebellum *
dc.subject.meshHeterozygote *
dc.subject.meshAging *
dc.subject.meshMice *
dc.subject.meshStem Cells *
dc.titleMild cerebellar neurodegeneration of aged heterozygous PCD mice increases cell fusion of Purkinje and bone marrow-derived cells.es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.3727/096368912X638900es_ES
dc.subject.unesco3207.11 Neuropatologíaes_ES
dc.subject.unesco2490 Neurocienciases_ES
dc.identifier.doi10.3727/096368912X638900
dc.relation.projectIDBFU2010-18284es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.pmid22507630
dc.identifier.essn1555-3892
dc.journal.titleCell transplantationes_ES
dc.volume.number21es_ES
dc.issue.number7es_ES
dc.page.initial1595es_ES
dc.page.final1602es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decscerebelo *
dc.subject.decsenfermedades neurodegenerativas *
dc.subject.decstrasplante de células madre *
dc.subject.decsanimales *
dc.subject.decsratones *
dc.subject.decscélulas de la médula ósea *
dc.subject.decscélulas madre *
dc.subject.decsfusión celular *
dc.subject.decsenvejecimiento *
dc.subject.decsdegeneración nerviosa *
dc.subject.decscélulas de Purkinje *
dc.subject.decsheterocigoto *


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