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dc.contributor.authorDas, Ridhima
dc.contributor.authorVirlan, Maria Justina Roxana
dc.contributor.authorXenaki, Victoria
dc.contributor.authorKulasekara, Keerthi Kumara
dc.contributor.authorLukandu, Ochiba Mohammed
dc.contributor.authorNeppelberg, Evelyn
dc.contributor.authorVintermyr, Olav Karsten
dc.contributor.authorJohannessen, Anne Christine
dc.contributor.authorCalenic, Bogdan
dc.contributor.authorCostea, Daniela Elena
dc.date.accessioned2022-06-08T06:55:52Z
dc.date.available2022-06-08T06:55:52Z
dc.date.created2022-05-14T16:42:11Z
dc.date.issued2022
dc.identifier.issn0909-8836
dc.identifier.urihttps://hdl.handle.net/11250/2997800
dc.description.abstractOral epithelial differentiation is known to be directed by underlying fibroblasts, but the responsible factor(s) have not been identified. We aimed here to identify fibroblast-derived factors responsible for oral epithelial differentiation. Primary normal human oral keratinocytes and fibroblasts were isolated from healthy volunteers after informed consent (n = 5) and 3D-organotypic (3D-OT) cultures were constructed. Various growth factors were added at a range of 0.1-100 ng/ml. 3D-OTs were harvested after ten days and assessed histologically, by immunohistochemistry and the TUNEL method. Epithelium developed in 3D-OT without fibroblasts showed an undifferentiated phenotype. Addition of granulocyte macrophage-colony stimulating factor (GM-CSF) induced expression of cytokeratin 13 in suprabasal cell layers. Admixture of GM-CSF and keratinocyte growth factor (KGF) induced, in addition, polarization of epidermal growth factor (EGF) receptor and β1-integrin to basal cell layer and collagen IV deposition. Terminal differentiation with polarization of TUNEL-positive cells to superficial layers occurred only in the presence of fibroblasts in collagen gels either in direct contact or at distance from normal oral keratinocytes. Taken together, these results show that major aspects of oral epithelial differentiation are regulated by the synergic combination of GM-CSF and KGF. However, the terminal stage seems to be controlled by other yet unidentified fibroblast-derived diffusible factor(s).en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleGranulocyte macrophage-colony stimulating factor and keratinocyte growth factor control of early stages of differentiation of oral epitheliumen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2022 the authorsen_US
dc.source.articlenumbere12867en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1111/eos.12867
dc.identifier.cristin2024613
dc.source.journalEuropean Journal of Oral Sciencesen_US
dc.identifier.citationEuropean Journal of Oral Sciences. 2022, 130 (3), e12867.en_US
dc.source.volume130en_US
dc.source.issue3en_US


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