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dc.date.accessioned2015-11-26T19:50:08Z
dc.date.available2015-11-26T19:50:08Z
dc.date.created2015-01-31T06:10:56Z
dc.date.issued2015
dc.identifier.citationUtheim, Øygunn Aass Islam, Rakibul Lyberg, Torstein Roald, Borghild Eidet, Jon Roger de la Paz, Maria Dartt, Darlene A. Raeder, Sten Utheim, Tor Paaske . Serum-Free and Xenobiotic-Free Preservation of Cultured Human Limbal Epithelial Cells. PLoS ONE. 2015
dc.identifier.urihttp://hdl.handle.net/10852/47900
dc.description.abstractAim/Purpose of the Study To develop a one-week storage method, without serum and xenobiotics, that would maintain cell viability, morphology, and phenotype of cultured human limbal epithelial sheets. Materials and Methods Human limbal explants were cultured on intact human amniotic membranes for two weeks. The sheets were stored in a hermetically sealed container at 23°C in either a serum-free medium with selected animal serum-derived compounds (Quantum 286) or a xenobiotic-free medium (Minimal Essential Medium) for 4 and 7 days. Stored and non-stored cultures were analyzed for cell viability, amniotic membrane and epithelial sheet thickness, and a panel of immunohistochemical markers for immature cells (ΔNp63α, p63, Bmi-1, C/EBP∂, ABCG2 and K19), differentiated cells (K3 and Cx43), proliferation (PCNA), and apoptosis (Caspase-3). Results The cell viability of the cultures was 98 ± 1% and remained high after storage. Mean central thickness of non-stored limbal epithelial sheets was 23 ± 3 μm, and no substantial loss of cells was observed after storage. The non-stored epithelial sheets expressed a predominantly immature phenotype with ΔNp63α positivity of more than 3% in 9 of 13 cultures. After storage, the expression of ABCG2 and C/EBP∂ was reduced for the 7 day Quantum 286-storage group; (P = 0.04), and Bmi-1 was reduced after 4 day Quantum 286-storage; (P = 0.02). No other markers varied significantly. The expression of differentiation markers was unrelated to the thickness of the epithelia and amniotic membrane, apart from ABCG2, which correlated negatively with thickness of limbal epithelia (R = -0.69, P = 0.01) and ΔNp63α, which correlated negatively with amniotic membrane thickness (R = -0.59, P = 0.03). Conclusion Limbal epithelial cells cultured from explants on amniotic membrane can be stored at 23°C in both serum-free and xenobiotic-free media, with sustained cell viability, ultrastructure, and ΔNp63α-positivity after both 4 and 7 days.en_US
dc.languageEN
dc.language.isoenen_US
dc.publisherPublic Library of Science (PLoS)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleSerum-Free and Xenobiotic-Free Preservation of Cultured Human Limbal Epithelial Cellsen_US
dc.typeJournal articleen_US
dc.creator.authorUtheim, Øygunn Aass
dc.creator.authorIslam, Rakibul
dc.creator.authorLyberg, Torstein
dc.creator.authorRoald, Borghild
dc.creator.authorEidet, Jon Roger
dc.creator.authorde la Paz, Maria
dc.creator.authorDartt, Darlene A.
dc.creator.authorRaeder, Sten
dc.creator.authorUtheim, Tor Paaske
cristin.unitcode185,50,0,0
cristin.unitnameDet medisinske fakultet
cristin.ispublishedfalse
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1213872
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS ONE&rft.volume=&rft.spage=&rft.date=2015
dc.identifier.jtitlePLoS ONE
dc.identifier.volume10
dc.identifier.issue3
dc.identifier.doi10.1371/journal.pone.0118517
dc.identifier.urnURN:NBN:no-51916
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1932-6203
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/47900/1/journal.pone.0118517.pdf
dc.type.versionPublishedVersion
cristin.articleide0118517


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