Show simple item record

dc.contributor.authorJanes, Sam M.
dc.contributor.authorOfstad, Tyler A.
dc.contributor.authorCampbell, Douglas H.
dc.contributor.authorWatt, Fiona M.
dc.contributor.authorProwse, David M.
dc.date.accessioned2015-07-16T23:10:32Z
dc.date.available2015-07-16T23:10:32Z
dc.date.issued2004-08-15
dc.identifier.citationJanes , S M , Ofstad , T A , Campbell , D H , Watt , F M & Prowse , D M 2004 , ' Transient activation of FOXN1 in keratinocytes induces a transcriptional programme that promotes terminal differentiation : Contrasting roles of FOXN1 and Akt ' , Journal of Cell Science , vol. 117 , no. 18 , pp. 4157-4168 . https://doi.org/10.1242/jcs.01302
dc.identifier.issn0021-9533
dc.identifier.otherPURE: 8733943
dc.identifier.otherPURE UUID: 02ff11b4-a55b-46d3-940f-f3551b46fec0
dc.identifier.otherScopus: 3543071500
dc.identifier.otherPubMed: 15316080
dc.identifier.urihttp://hdl.handle.net/2299/16168
dc.description.abstractThe forkhead transcription factor FOXN1 is required for normal cutaneous and thymic epithelial development. Mutations in FOXN1 give rise to the nude phenotype in mice, rats and man. However, the genes that are regulated by FOXN1 are unknown. To investigate FOXN1 function we expressed an inducible form of the protein, FOXN1ER, that is activated by 4-hydroxytamoxifen in primary human epidermal keratinocytes. Transient activation of FOXN1 decreased the proportion of keratinocytes that formed actively growing clones attributable to stem cell founders and increased the number of abortive clones, without inducing apoptosis. Within 24 hours the majority of cells had initiated terminal differentiation, as assessed by involucrin expression. We performed a cDNA microarray experiment to analyse changes in the transcription of approximately 6000 genes. Following FOXN1 activation we detected increases of two fold or greater in the RNA levels of over 30 genes. Genes promoting growth arrest, survival and differentiation featured prominently and markers of early events in keratinocyte differentiation were also detected. Since one of the induced genes was Akt we investigated whether Akt played a role in terminal differentiation. Activation of PI 3-kinase but not Akt was necessary for FOXN1-induced differentiation. In reconstituted epidermis FOXN1 promoted early stages of terminal differentiation whereas Akt activation was sufficient to induce late stages, including formation of the cornified layers. These results establish a role for FOXN1 in initiation of terminal differentiation and implicate Akt in subsequent events.en
dc.format.extent12
dc.language.isoeng
dc.relation.ispartofJournal of Cell Science
dc.subjectAkT
dc.subjectFOXN1
dc.subjectMicroarray
dc.subjectPI 3-kinase
dc.subjectStem cells
dc.subjectCell Biology
dc.titleTransient activation of FOXN1 in keratinocytes induces a transcriptional programme that promotes terminal differentiation : Contrasting roles of FOXN1 and Akten
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionDepartment of Human and Environmental Sciences
dc.contributor.institutionHealth & Human Sciences Research Institute
dc.description.statusPeer reviewed
dc.relation.school
dcterms.dateAccepted2004-08-15
rioxxterms.versionVoR
rioxxterms.versionofrecordhttps://doi.org/10.1242/jcs.01302
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record