Regulation of NR4A by nutritional status, gender, postnatal development and hormonal deficiency

dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Medicina Molecular e Enfermidades Crónicasgl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Fisioloxíagl
dc.contributor.authorPérez Sieira, Sonia
dc.contributor.authorLópez Pérez, Miguel A.
dc.contributor.authorNogueiras Pozo, Rubén
dc.contributor.authorTovar Carro, Sulay A.
dc.date.accessioned2020-06-23T10:41:39Z
dc.date.available2020-06-23T10:41:39Z
dc.date.issued2015
dc.description.abstractThe NR4A is a subfamily of the orphan nuclear receptors (NR) superfamily constituted by three well characterized members: Nur77 (NR4A1), Nurr1 (NR4A2) and Nor 1 (NR4A3). They are implicated in numerous biological processes as DNA repair, arteriosclerosis, cell apoptosis, carcinogenesis and metabolism. Several studies have demonstrated the role of this subfamily on glucose metabolism, insulin sensitivity and energy balance. These studies have focused mainly in liver and skeletal muscle. However, its potential role in white adipose tissue (WAT), one of the most important tissues involved in the regulation of energy homeostasis, is not well-studied. The aim of this work was to elucidate the regulation of NR4A in WAT under different physiological and pathophysiological settings involved in energy balance such as fasting, postnatal development, gender, hormonal deficiency and pregnancy. We compared NR4A mRNA expression of Nur77, Nurr1 and Nor 1 and found a clear regulation by nutritional status, since the expression of the 3 isoforms is increased after fasting in a leptin-independent manner and sex steroid hormones also modulate NR4A expression in males and females. Our findings indicate that NR4A are regulated by different physiological and pathophysiological settings known to be associated with marked alterations in glucose metabolism and energy status.gl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThis work has been supported by grants from Fondo Investigaciones Sanitarias (ST: PI12/02842), Ministerio de Economia y Competitividad (RN: RYC-2008-02219 and BFU2012-35255; MMM: BFU2010-17116), Xunta de Galicia (ML: 10PXIB208164PR and 2012-CP070; RN: EM 2012/039 and 2012-CP069), Centro de Investigación Biomédica en Red (CIBER) de Fisiopatología de la Obesidad y Nutrición. CIBERobn is an initiative of the Instituto de Salud Carlos III (ISCIII) of Spain which is supported by FEDER funds. The research leading to these results has also received funding from the European Community's Seventh Framework Programme under the following grant: ML and RN: FP7/2007-2013: n° 245009: NeuroFASTgl
dc.identifier.citationPérez-Sieira, S., López, M., Nogueiras, R. et al. Regulation of NR4A by nutritional status, gender, postnatal development and hormonal deficiency. Sci Rep 4, 4264 (2015). https://doi.org/10.1038/srep04264gl
dc.identifier.doi10.1038/srep04264
dc.identifier.essn2045-2322
dc.identifier.urihttp://hdl.handle.net/10347/23052
dc.language.isoenggl
dc.publisherNature Publishing Groupgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/245009
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN/Plan Nacional de I+D+i 2008-2011/RYC-2008-02219/ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN/Plan Nacional de I+D+i 2008-2011/BFU2010-17116/ES/CARACTERIZACION DE NUEVOS MARCADORES REGULADORES DEL FUNCIONAMIENTO DEL TEJIDO ADIPOSO
dc.relation.publisherversionhttps://doi.org/10.1038/srep04264gl
dc.rights© 2014 The author(s). This work is licensed under a Creative Commons AttributionNonCommercial-ShareAlike 3.0 Unported license. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0gl
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0
dc.subjectEndocrinologygl
dc.subjectHomeostasisgl
dc.titleRegulation of NR4A by nutritional status, gender, postnatal development and hormonal deficiencygl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
relation.isAuthorOfPublicationfe6af4cf-b6e2-49b2-a988-f647d5091171
relation.isAuthorOfPublication65efc211-9a43-4312-8e7f-88b812cf2ae1
relation.isAuthorOfPublication5740f5b3-5af4-4a61-9d24-c8b9d0508177
relation.isAuthorOfPublication.latestForDiscovery65efc211-9a43-4312-8e7f-88b812cf2ae1

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