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dc.contributor.authorTra, Wendy M. W.
dc.contributor.authorW. van Neck, Johan
dc.contributor.authorE. R. Hovius, Steven
dc.contributor.authorJ. V. M. van Osch, Gerjo
dc.contributor.authorPerez Amodio, Soledad
dc.date.accessioned2025-07-08T09:52:08Z
dc.date.available2025-07-08T09:52:08Z
dc.date.issued2012
dc.identifier.citationTra, Wendy M. W.; W. van Neck, Johan; E. R. Hovius, Steven [et al.]. Characterization of a three-dimensional mucosal equivalent: similarities and differences with native oral mucosa. Cells Tissues Organs, 2012, 195 (3), p. 185–196. Disponible en: <https://karger.com/cto/article-abstract/195/3/185/91220/Characterization-of-a-Three-Dimensional-Mucosal?redirectedFrom=fulltext>. Fecha de acceso: 8 jul. 2025. DOI: 10.1159/000324918ca
dc.identifier.issn1422-6421ca
dc.identifier.urihttp://hdl.handle.net/20.500.12328/4941
dc.description.abstractThe aim of this study was to create and characterize a tissue-engineered mucosal equivalent (TEM) that closely resembles native mucosa. TEM consists of human primary keratinocytes and fibroblasts isolated from biopsies taken from healthy donors and seeded onto a de-epidermized dermis and cultured for 14 days at the air/liquid interface. The structure of TEM was examined and compared with native nonkeratinizing oral mucosa (NNOM). The various components of the newly formed epidermal layer, basement membrane and underlying connective tissue were analyzed using immunohistochemistry. The mucosal substitute presented in this study showed a mature stratified squamous epithelium that was similar to that of native oral mucosa, as demonstrated by K19, desmoglein-3 and involucrin staining. In addition, the expression of basement membrane components collagen type IV, laminin-5 and integrin α6 and β4 in TEM proved to be consistent with native oral mucosa. The expression of PAS, Ki67, K10 and K13, however, appeared to be different in TEM compared to NNOM. Nevertheless, the similarities with native oral mucosa makes TEM a promising tool for studying the biology of mucosal pathologies such as oral mucositis or fibrosis as well as the development of new therapies.ca
dc.format.extent11ca
dc.language.isoengca
dc.publisherKargen Publishersca
dc.relation.ispartofCells Tissues Organsca
dc.relation.ispartofseries195;3
dc.rights© 2011 S. Karger AG, Baselca
dc.subject.otherEnginyeria de teixitsca
dc.subject.otherMucosa oralca
dc.subject.otherQueratinòcitsca
dc.subject.otherFibroblastsca
dc.subject.otherIngeniería de tejidosca
dc.subject.otherMucosa oralca
dc.subject.otherQueratinocitoca
dc.subject.otherFibroblastoca
dc.subject.otherTissue engineeringca
dc.subject.otherOral mucosaca
dc.subject.otherKeratinocyteca
dc.subject.otherFibroblastca
dc.titleCharacterization of a three-dimensional mucosal equivalent: similarities and differences with native oral mucosaca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.subject.udc57ca
dc.identifier.doihttps://dx.doi.org/10.1159/000324918ca


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