Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/164827
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dc.contributor.authorMarín, Sandra-
dc.contributor.authorEstil·les Altimiras, Elisabet-
dc.contributor.authorLladó Garriga, Laura-
dc.contributor.authorSan José, Patricia-
dc.contributor.authorNacher, Montserrat-
dc.contributor.authorTéllez i Besolí, Noèlia-
dc.contributor.authorMontanya Mias, Eduard-
dc.date.accessioned2020-06-08T15:38:04Z-
dc.date.available2020-06-08T15:38:04Z-
dc.date.issued2019-07-19-
dc.identifier.issn1932-6203-
dc.identifier.urihttp://hdl.handle.net/2445/164827-
dc.description.abstractAim: To evaluate the effect of pancreatic ductal cells on experimental human islet transplantation. Materials and methods: Isolated islets were additionally purified by handpicking. Ductal cells were purified by magnetic cell sorting and then clustered into ductal pancreatospheres (DPS). Islets, DPS, and islets + DPS (100 islets + 75 DPS, or 100 islets + 200 DPS) were cultured and glucose-stimulated insulin secretion, β-cell apoptosis, and gene expression was determined. Islets and islets + DPS preparations (800 islets + 600 DPS) were transplanted to streptozotocin-treated immunodeficient mice and glycemia, graft morphometry, and gene expression were determined. Results: Insulin stimulation index was higher in islets than in islets co-cultured with DPS (5.59 ± 0.93 vs 4.02 ± 0.46; p<0.05). IL1B and CXCL11 expression was higher in 100 islets + 200 DPS than in islets (p<0.01), and IL-1β was detected in supernatants collected from DPS and islets + DPS preparations, but not in islets. Hyperglycemia developed in 33% and 67% of mice transplanted with islets or with islets + DPS respectively. β-cell mass was 26% lower in islets + DPS than in islets grafts (p>0.05), and the ratio β-/endocrine non-β-cell mass was lower in islets + DPS grafts (islets: 2.05 ± 0.18, islets + DPS: 1.35 ± 0.15; p<0.01). IL1B and IL1RN expression was significantly higher in islets + DPS grafts. Conclusions: Islet preparations enriched with ductal cells have a lower insulin stimulation index in vitro and achieved a worse metabolic outcome after transplantation. Inflammation may mediate the deleterious effects of ductal cells on islet cells.-
dc.format.extent16 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherPublic Library of Science (PLoS)-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1371/journal.pone.0220064-
dc.relation.ispartofPLoS One, 2019, vol. 14, num. 7, p. e0220064-
dc.relation.urihttps://doi.org/10.1371/journal.pone.0220064-
dc.rightscc-by (c) Marín, Sandra et al., 2019-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es-
dc.sourceArticles publicats en revistes (Ciències Clíniques)-
dc.subject.classificationIllots de Langerhans-
dc.subject.classificationInsulina-
dc.subject.otherIslands of Langerhans-
dc.subject.otherInsulin-
dc.titlePancreatic ductal cells may have a negative effect on human islet transplantation. PLoS One. 2019 Jul 19;14(7):e0220064.-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec695233-
dc.date.updated2020-06-08T15:38:04Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Ciències Clíniques)

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