Limbal stromal cells derived from porcine tissue demonstrate mesenchymal characteristics in vitro

dc.bibliographicCitation.firstPage6377
dc.bibliographicCitation.issue1
dc.bibliographicCitation.journalTitleScientific Reportseng
dc.bibliographicCitation.volume7
dc.contributor.authorFernández-Pérez, Julia
dc.contributor.authorBinner, Marcus
dc.contributor.authorWerner, Carsten
dc.contributor.authorBray, Laura J.
dc.date.accessioned2023-04-27T11:59:29Z
dc.date.available2023-04-27T11:59:29Z
dc.date.issued2017
dc.description.abstractLimbal stromal cells (LSCs) from the human ocular surface display mesenchymal stromal cell characteristics in vitro. In this study, we isolated cells from the porcine limbal stroma (pLSCs), characterised them, and evaluated their ability to support angiogenesis and the culture of porcine limbal epithelial stem cells (pLESCs). The isolated cells adhered to plastic and grew in monolayers in vitro using serum-supplemented or serum-free medium. The pLSCs demonstrated expression of CD29, and cross-reactivity with anti-human CD45, CD90, CD105, CD146, and HLA-ABC. However, expression of CD105, CD146 and HLA-ABC reduced when cultured in serum-free medium. PLSCs did not undergo adipogenic or osteogenic differentiation, but differentiated towards the chondrogenic lineage. Isolated cells were also co-cultured with human umbilical vein endothelial cells (HUVECs) in star-shaped Poly(ethylene glycol) (starPEG)-heparin hydrogels to assess their pericyte capacity which supported angiogenesis networks of HUVECs. PLSCs supported the three dimensional HUVEC network for 7 days. The isolated cells were further growth-arrested and evaluated as feeder cells for pLESC expansion on silk fibroin membranes, as a potential carrier material for transplantation. PLSCs supported the growth of pLESCs comparably to murine 3T3 cells. In conclusion, although pLSCs were not completely comparable to their human counterpart, they display several mesenchymal-like characteristics in vitro.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/12126
dc.identifier.urihttp://dx.doi.org/10.34657/11160
dc.language.isoeng
dc.publisherLondon : Nature Publishing Group
dc.relation.doihttps://doi.org/10.1038/s41598-017-06898-2
dc.relation.essn2045-2322
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subject.ddc500
dc.subject.ddc600
dc.subject.otherAnimalseng
dc.subject.otherCell Adhesioneng
dc.subject.otherCell Culture Techniqueseng
dc.subject.otherCell Differentiationeng
dc.subject.otherCell Proliferationeng
dc.subject.otherCells, Culturedeng
dc.subject.otherCoculture Techniqueseng
dc.subject.otherFeeder Cellseng
dc.subject.otherHuman Umbilical Vein Endothelial Cellseng
dc.subject.otherHumanseng
dc.subject.otherIntegrin beta1eng
dc.subject.otherLimbus Corneaeeng
dc.subject.otherMesenchymal Stem Cellseng
dc.subject.otherMiceeng
dc.subject.otherNeovascularization, Physiologiceng
dc.subject.otherNIH 3T3 Cellseng
dc.subject.otherStromal Cellseng
dc.subject.otherSwineeng
dc.titleLimbal stromal cells derived from porcine tissue demonstrate mesenchymal characteristics in vitroeng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccess
wgl.contributorIPF
wgl.subjectBiowissenschaften/Biologieger
wgl.typeZeitschriftenartikelger
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