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dc.contributor.authorMora-Castilla, Sergio-
dc.contributor.authorTejedo Huamán, Juan Rigoberto-
dc.contributor.authorTapia-Limonchi, Rafael-
dc.contributor.authorDíaz, Irene-
dc.contributor.authorHitos, Ana B.-
dc.contributor.authorCahuana, Gladys M.-
dc.contributor.authorHmadcha, Abdelkrim-
dc.contributor.authorMartín, Franz-
dc.contributor.authorSoria Escoms, Bernat-
dc.contributor.authorBedoya Bergua, Francisco Javier-
dc.date.accessioned2015-10-20T10:42:19Z-
dc.date.available2015-10-20T10:42:19Z-
dc.date.issued2014-12-03-
dc.identifierdoi: 10.1155/2014/379678-
dc.identifierissn: 1687-9678-
dc.identifier.citationStem Cells International 2014: 379678 (2014)-
dc.identifier.urihttp://hdl.handle.net/10261/123596-
dc.description.abstractThe function of pluripotency genes in differentiation is a matter of investigation. We report here that Nanog and Oct4 are reexpressed in two mouse embryonic stem cell (mESC) lines following exposure to the differentiating agent DETA/NO. Both cell lines express a battery of both endoderm and mesoderm markers following induction of differentiation with DETA/NO-based protocols. Confocal analysis of cells undergoing directed differentiation shows that the majority of cells expressing Nanog express also endoderm genes such as Gata4 and FoxA2 (75.4% and 96.2%, resp.). Simultaneously, mRNA of mesodermal markers Flk1 and Mef2c are also regulated by the treatment. Acetylated histone H3 occupancy at the promoter of Nanog is involved in the process of reexpression. Furthermore, Nanog binding to the promoter of Brachyury leads to repression of this gene, thus disrupting mesendoderm transition-
dc.description.sponsorshipThis work was supported by Consejería de Igualdad, Salud y Políticas Sociales, Junta de Andalucía (PI0022/2008, PI105/ 2010, and PI10/00964), Consejer´ıa de Economía, Innovación, Ciencia y Empleo, Junta de Andalucía (CTS-7127/2011, P10.CTS.6505, and PAI BIO-311), Instituto de Salud Carlos III/FEDER (Red TerCel, RD06/0010/0025, RD12/0019/0028), Ministerio de Economía y Competitividad (IPT-2011-1615- 900000), Ministerio de Salud y Consumo (TRA-120), and Servicio Andaluz de Salud (SAS 11245)-
dc.publisherHindawi Publishing Corporation-
dc.relation.isversionofPublisher's version-
dc.rightsopenAccess-
dc.titleTransient Downregulation of Nanog and Oct4 Induced by DETA/NO Exposure in Mouse Embryonic Stem Cells Leads to Mesodermal/Endodermal Lineage Differentiation-
dc.typeartículo-
dc.identifier.doi10.1155/2014/379678-
dc.relation.publisherversionhttp://dx.doi.org/10.1155/2014/379678-
dc.date.updated2015-10-20T10:42:20Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.rights.licensehttp://creativecommons.org/licenses/by/3.0/-
dc.contributor.funderJunta de Andalucía-
dc.contributor.funderInstituto de Salud Carlos III-
dc.contributor.funderEuropean Commission-
dc.contributor.funderRed de Terapia Celular (España)-
dc.contributor.funderMinisterio de Economía y Competitividad (España)-
dc.contributor.funderMinisterio de Sanidad y Consumo (España)-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004587es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100011011es_ES
dc.identifier.pmid25544848-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
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