Cell viability assay in corneal endothelium

UDC.coleccionInvestigaciónes_ES
UDC.conferenceTitleII Annual Meeting CINBIOes_ES
UDC.departamentoFisioterapia, Medicina e Ciencias Biomédicases_ES
UDC.grupoInvTerapia Celular e Medicina Rexenerativa (INIBIC)es_ES
UDC.grupoInvGrupo de Investigación en Terapia Celular e Medicina Rexenerativa (TCMR)es_ES
UDC.institutoCentroINIBIC - Instituto de Investigacións Biomédicas de A Coruñaes_ES
dc.contributor.authorRodríguez-Fernández, Silvia
dc.contributor.authorÁlvarez Portela, Marcelino
dc.contributor.authorRendal-Vázquez, Esther
dc.contributor.authorMontero-Salinas, Alejandro
dc.contributor.authorPiñeiro-Ramil, María
dc.contributor.authorCastro Viñuelas, Rocío
dc.contributor.authorRojas, María Victoria de
dc.contributor.authorSánchez Ibáñez, Jacinto
dc.contributor.authorFuentes Boquete, Isaac Manuel
dc.contributor.authorDíaz-Prado, Silvia
dc.date.accessioned2019-03-13T09:14:11Z
dc.date.available2019-03-13T09:14:11Z
dc.date.issued2018
dc.descriptionResumen del póster publicado en el II Annual Meeting CINBIO abstracts book [Internet], p. 65es_ES
dc.description.abstract[Abstract] Introduction: Endothelium is the inner layer of the cornea, which must be viable for transplanting. The limited availability of corneas makes necessary the developing of preservation techniques that allow a long storage without losing endothelial viability.Objectives: Optimization of a cell viability assay in preserved corneas.Methods: One half of an endothelium from a cornea that was storage in hypothermic conditions and an endothelium of a cryopreserved cornea were stained with LIVE/DEAD imaging kit and Hoechst. The other half of endothelium was the negative control. Corneal endothelia were imaged using a fluorescence microscope.Results: Four sort of cells were visualized on both endothelia: viable cells with high esterase activity, intermediate cells with low esterase activity, non-viable cells without esterase activity, and cells only stained by Hoechst. Conclusions: Triple stain is effectiveto detect different sort of cells in endothelium of preserved corneas, included viable cells, depending on their esterase enzymatic activity and on cell and nuclear membrane damage.es_ES
dc.identifier.citationRodríguez-Fernández S, Álvarez-Portela M, Rendal-Vázquez ME, et al. Cell viability assay in corneal endothelium. Póster presentado en: II Annual Meeting CINBIO; 2018 Jun 25-25; Vigo, Españaes_ES
dc.identifier.urihttp://hdl.handle.net/2183/22204
dc.language.isoenges_ES
dc.rights.accessRightsopen accesses_ES
dc.titleCell viability assay in corneal endotheliumes_ES
dc.typeconference outputes_ES
dspace.entity.typePublication
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