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dc.contributor.authorGarcía-Bonilla, María
dc.contributor.authorOjeda-Pérez, Betsaida
dc.contributor.authorGarcía-Martín, María Luisa
dc.contributor.authorMuñoz-Hernández, María del Carmen
dc.contributor.authorVitorica Ferrández, Javier
dc.contributor.authorJiménez, Sebastián
dc.contributor.authorCifuentes-Rueda, Manuel 
dc.contributor.authorSantos-Ruiz, Leonor 
dc.contributor.authorShumilov, Kirill
dc.contributor.authorClaros-Gil, Silvia 
dc.contributor.authorGutiérrez-Pérez, Antonia 
dc.contributor.authorPáez-González, Patricia 
dc.date.accessioned2024-02-20T07:45:06Z
dc.date.available2024-02-20T07:45:06Z
dc.date.created2024
dc.date.issued2020-03-17
dc.identifier.citationGarcía-Bonilla, M., Ojeda-Pérez, B., García-Martín, M.L. et al. Neocortical tissue recovery in severe congenital obstructive hydrocephalus after intraventricular administration of bone marrow-derived mesenchymal stem cells. Stem Cell Res Ther 11, 121 (2020).es_ES
dc.identifier.urihttps://hdl.handle.net/10630/30530
dc.description.abstractIn obstructive congenital hydrocephalus, cerebrospinal fluid accumulation is associated with high intracranial pressure and the presence of periventricular edema, ischemia/hypoxia, damage of the white matter, and glial reactions in the neocortex. The viability and short time effects of a therapy based on bone marrow-derived mesenchymal stem cells (BM-MSC) have been evaluated in such pathological conditions in the hyh mouse model. moBM-MSC expressing fluorescent mRFP1 protein were injected into the lateral ventricle of hydrocephalic hyh mice. The effect in the neocortex was compared with hydrocephalic hyh mice injected with the vehicle and non-hydrocephalic littermates. Neural cell populations and the possibility of transdifferentiation were analyzed. Tissue recovering was investigated by H-1 HR-MAS NMR spectroscopy, thus allowing the detection of metabolites/osmolytes related with hydrocephalus severity and outcome in the neocortex. An in vitro assay to simulate the periventricular astrocyte reaction conditions was performed using BM-MSC under high TNF alpha level condition. The secretome in the culture medium was analyzed in this assay. Four days after transplantation, BM-MSC were found undifferentiated and scattered into the astrocyte reaction present in the damaged neocortex white matter. Tissue rejection to the integrated BM-MSC was not detected 4 days after transplantation. Hyh mice transplanted with BM-MSC showed a reduction in the apoptosis in the periventricular neocortex walls, suggesting a neuroprotector effect of the BM-MSC in these conditions. A decrease in the levels of metabolites/osmolytes in the neocortex, such as taurine and neuroexcytotoxic glutamate, also indicated a tissue recovering. Under high TNF alpha level condition in vitro, BM-MSC showed an upregulation of cytokine and protein secretion that may explain homing, immunomodulation, and vascular permeability, and therefore the tissue recovering.es_ES
dc.description.sponsorshipInstituto de Salud Carlos III (PI15/00619; PI19/00778; PI15/00796 y PI18/01557) Ministerio de Economía y Competitividad - MINECO (RYC-2014-16980) Ministerio de Educación, Cultura y Deporte - MECD (FPU13/02906)es_ES
dc.language.isoenges_ES
dc.publisherBMCes_ES
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectHidrocefaliaes_ES
dc.subjectCélulas madrees_ES
dc.subjectAstrocitoses_ES
dc.subjectEspectroscopíaes_ES
dc.subject.otherHydrocephaluses_ES
dc.subject.otherBone Marrow-derived Mesenchymal Stem Cellses_ES
dc.subject.otherBM-MSCes_ES
dc.subject.otherReactive astrocyteses_ES
dc.subject.otherSpectroscopyes_ES
dc.subject.otherHop Gait HYHes_ES
dc.subject.otherStromal cellses_ES
dc.subject.otherEpendymal denudationes_ES
dc.titleNeocortical tissue recovery in severe congenital obstructive hydrocephalus after intraventricular administration of bone marrow-derived mesenchymal stem cells.es_ES
dc.typejournal articlees_ES
dc.centroFacultad de Cienciases_ES
dc.identifier.doi10.1186/s13287-020-01626-6
dc.type.hasVersionVoRes_ES
dc.departamentoBiología Celular, Genética y Fisiología
dc.rights.accessRightsopen accesses_ES


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