Biofabrication of a Tubular Model of Human Urothelial Mucosa Using Human Wharton Jelly Mesenchymal Stromal Cells.

dc.contributor.authorGarzón, Ingrid
dc.contributor.authorJaimes-Parra, Boris Damián
dc.contributor.authorPascual-Geler, Manrique
dc.contributor.authorCózar, José Manuel
dc.contributor.authorSánchez-Quevedo, María Del Carmen
dc.contributor.authorMosquera-Pacheco, María Auxiliadora
dc.contributor.authorSánchez-Montesinos, Indalecio
dc.contributor.authorFernández-Valadés, Ricardo
dc.contributor.authorCampos, Fernando
dc.contributor.authorAlaminos, Miguel
dc.date.accessioned2025-01-07T17:02:02Z
dc.date.available2025-01-07T17:02:02Z
dc.date.issued2021-05-13
dc.description.abstractSeveral models of bioartificial human urothelial mucosa (UM) have been described recently. In this study, we generated novel tubularized UM substitutes using alternative sources of cells. Nanostructured fibrin-agarose biomaterials containing fibroblasts isolated from the human ureter were used as stroma substitutes. Then, human Wharton jelly mesenchymal stromal cells (HWJSC) were used to generate an epithelial-like layer on top. Three differentiation media were used for 7 and 14 days. Results showed that the biofabrication methods used here succeeded in generating a tubular structure consisting of a stromal substitute with a stratified epithelial-like layer on top, especially using a medium containing epithelial growth and differentiation factors (EM), although differentiation was not complete. At the functional level, UM substitutes were able to synthesize collagen fibers, proteoglycans and glycosaminoglycans, although the levels of control UM were not reached ex vivo. Epithelial differentiation was partially achieved, especially with EM after 14 days of development, with expression of keratins 7, 8, and 13 and pancytokeratin, desmoplakin, tight-junction protein-1, and uroplakin 2, although at lower levels than controls. These results confirm the partial urothelial differentiative potential of HWJSC and suggest that the biofabrication methods explored here were able to generate a potential substitute of the human UM for future clinical use.
dc.identifier.doi10.3390/polym13101568
dc.identifier.essn2073-4360
dc.identifier.pmcPMC8153323
dc.identifier.pmid34068343
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC8153323/pdf
dc.identifier.unpaywallURLhttps://www.mdpi.com/2073-4360/13/10/1568/pdf?version=1620974722
dc.identifier.urihttps://hdl.handle.net/10668/28138
dc.issue.number10
dc.journal.titlePolymers
dc.journal.titleabbreviationPolymers (Basel)
dc.language.isoen
dc.organizationInstituto de Investigación Biosanitaria de Granada (ibs.GRANADA)
dc.organizationInstituto de Investigación Biosanitaria de Granada (ibs.GRANADA)
dc.organizationSAS - Hospital Universitario Virgen de las Nieves
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectbiofabrication
dc.subjecthuman Wharton jelly mesenchymal stromal cells
dc.subjecturothelial mucosa
dc.titleBiofabrication of a Tubular Model of Human Urothelial Mucosa Using Human Wharton Jelly Mesenchymal Stromal Cells.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number13

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