Afficher la notice abrégée

dc.contributor.authorSrivastava, Girish K.
dc.contributor.authorMartín, Laura
dc.contributor.authorSingh, Amar K.
dc.contributor.authorFernandez‐Bueno, Ivan
dc.contributor.authorGayoso, Manuel J.
dc.contributor.authorGarcia‐Gutierrez, Maria T.
dc.contributor.authorGirotti, Alessandra
dc.contributor.authorAlonso, Matilde
dc.contributor.authorRodríguez‐Cabello, José C.
dc.contributor.authorPastor, José C.
dc.date.accessioned2026-02-17T10:33:32Z
dc.date.available2026-02-17T10:33:32Z
dc.date.issued2011
dc.identifier.citationJ Biomed Mater Res Part A, Volume 97A, Issue3 1 June 2011 Pages 243-250es
dc.identifier.issn1549-3296es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/82819
dc.description.abstractThe aim of this study is to investigate the use of elastin-like recombinamers (ELRs) as a substrate that can maintain the growth, phenotype, and functional characteristics of retinal pigment epithelial (RPE) cells efficiently and as a suitable carrier for the transplantation of autologous RPE cells for treatment of age-related macular degeneration (AMD). ELR films containing a bioactive sequence, RGD (ELR-RGD), and one with no specific sequence (ELR-IK) as control, were obtained by solvent-casting onto glass and subsequent cross-linking. ARPE19 cells were seeded on sterilized ELR films as well as on the control surfaces. Cells were analysed after 4, 24, 72, and 120 h to study cell adhesion, proliferation, cell viability, morphology, and specificity by staining with Trypan blue, DAPI, Rhodamin-Phalloidin and RPE65, ZO-1 antibodies and observing under fluorescence as well as electron microscope. ARPE19 cells seeded on both ELR films and controls were 100% viable and maintained their morphology and set of characteristics at the different time points studied. Cell proliferation on ELR-RGD was significantly higher than that found on ELR-IK at all time points, although it was less than the growth rate on polystyrene. ARPE19 cells grow well on ELR-RGD maintaining their phenotype. These results should be extended to further studies with fresh human RPE cells and in vivo studies to determine whether this ELR-RGD matrix could be used as a Bruch's membrane prosthesis and carrier for transplantation of RPE cells in patients suffering with AMD.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherWileyes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.titleElastin‐like recombinamers as substrates for retinal pigment epithelial cell growthes
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1002/jbm.a.33050es
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/10.1002/jbm.a.33050es
dc.identifier.publicationfirstpage243es
dc.identifier.publicationissue3es
dc.identifier.publicationlastpage250es
dc.identifier.publicationtitleJournal of Biomedical Materials Research Part Aes
dc.identifier.publicationvolume97Aes
dc.peerreviewedSIes
dc.description.projectThe authors would also like to thank Alicia Rodríguez Gascón, University of País Vasco (Spain), for providing the ARPE19 cells, and Cristhian Urzua Salinas and Jesús Gómez Escudero for their help.es
dc.identifier.essn1552-4965es
dc.type.hasVersioninfo:eu-repo/semantics/submittedVersiones


Fichier(s) constituant ce document

Thumbnail

Ce document figure dans la(les) collection(s) suivante(s)

Afficher la notice abrégée