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dc.contributor.authorAlió del Barrio, Jorge-
dc.contributor.authorChiesa, Massimo-
dc.contributor.authorGaragorri, Nerea-
dc.contributor.authorGarcia-Urquia, Nerea-
dc.contributor.authorFernandez-Delgado, Jorge-
dc.contributor.authorBataille, Laurent-
dc.contributor.authorRodriguez, Alejandra-
dc.contributor.authorArnalich-Montiel, Francisco-
dc.contributor.authorZarnowski, Tomasz-
dc.contributor.authorAlvarez de Toledo, Juan P.-
dc.contributor.authorAlio, Jorge L.-
dc.contributor.authorDe Miguel, Maria P.-
dc.contributor.otherDepartamentos de la UMH::Patología y Cirugíaes_ES
dc.date.accessioned2025-01-26T18:35:58Z-
dc.date.available2025-01-26T18:35:58Z-
dc.date.created2015-03-
dc.identifier.citationExp Eye Res . 2015 Mar:132:91-100es_ES
dc.identifier.issn0014-4835-
dc.identifier.urihttps://hdl.handle.net/11000/35350-
dc.description.abstractPurpose: To evaluate the in vivo biocompatibility of grafts composed of sheets of decellularized human corneal stroma with or without the recellularization of human adipose derived adult stem cells (h- ADASC) into the rabbit cornea. Methods: Sheets of human corneal stroma of 90 mm thickness were decellularized, and their lack of cytotoxicity was assayed. The recellularization was achieved by the injection of 2 105 labeled h-ADASC in the graft followed by five days of cell culture. The grafts were implanted in vivo into a stromal pocket at 50% depth. After a triple-masked three-month follow-up, the animals were euthanized and the biointegration of the graft, the viability of the stem cells and the expression of keratocan (human keratocyte-specific protein) were assessed. Results: The decellularized stromal sheets showed an intact extracellular matrix with a decellularization rate of 92.8% and an excellent recellularization capacity in vitro with h-ADASC. A complete and stable graft transparency was observed during the full follow-up, with absence of any clinical sign of rejection. The postmortem analysis demonstrated the survival of the transplanted human stem cells inside the graft and their differentiation into functional keratocytes, as assessed by the expression of human keratocan. Conclusions: We report a new model of lamellar keratoplasty that requires only a simple and safe procedure of liposuction and a donor allogeneic cornea to provide an optically transparent autologous stromal graft with excellent biocompatibility and integration into the host tissue in a rabbit modeles_ES
dc.formatapplication/pdfes_ES
dc.format.extent10es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/closedAccesses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectadipose derived stem cellses_ES
dc.subjectcorneaes_ES
dc.subjectdecellularizationes_ES
dc.subjectrecellularizationes_ES
dc.subjectlamellar corneal transplantes_ES
dc.subjectcorneal stroma regenerationes_ES
dc.subjecttissue engineeringes_ES
dc.titleAcellular human corneal matrix sheets seeded with human adipose-derived mesenchymal stem cells integrate functionally in an experimental animal modeles_ES
dc.title.alternativeAcellular human corneal matrix sheets seeded with human adipose-derived mesenchymal stem cells integrate functionally in an experimental animal modeles_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversion10.1016/j.exer.2015.01.020es_ES
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Artículos Patología y Cirugía


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