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dc.contributor.authorIglesias Osma, María Carmen 
dc.contributor.authorBlanco Barco, Enrique José 
dc.contributor.authorCarretero Hernández, Marta
dc.contributor.authorCatalano Iniesta, Leonardo 
dc.contributor.authorSánchez Robledo, Virginia
dc.contributor.authorGarcía Barrado, Josefa 
dc.contributor.authorVicente García, Teresa 
dc.contributor.authorBurks, Deborah J.
dc.contributor.authorCarretero González, José 
dc.date.accessioned2026-01-08T15:28:07Z
dc.date.available2026-01-08T15:28:07Z
dc.date.issued2019-04-05
dc.identifier.citationIglesias-Osma, M. C., Blanco, E. J., Carretero-Hernandez, M., Catalano-Iniesta, L., Sanchez-Robledo, V., Garcia-Barrado, M. J., Vicente-Garcia, T., Burks, D. J., & Carretero, J. (2019). The influence of the lack of insulin receptor substrate 2 (IRS2) on the thyroid gland. Scientific Reports, 9(1). https://doi.org/10.1038/S41598-019-42198-7es_ES
dc.identifier.urihttp://hdl.handle.net/10366/168554
dc.description.abstract[EN]Involvement of IRS2 in the proliferative effects of IGF-I of follicular thyroid cells has been described, but there are no evidences for in vivo participation of IRS2. This study aimed to analyse the in vivo relevance of IRS2 in the proliferation and apoptosis of thyroid cells by immunocytochemical studies for PCNA, Ki67, and active-caspase-3 in thyroid cells of IRS2 knockout (IRS2-KO) mice, jointly to TUNEL assay. Thyroid hormones were lower in IRS2-KO mice than in their wild-type (WT) counterparts. Increases in the area, perimeter and diameter of thyroid follicles of IRS2-KO mice were observed, which also showed increased proliferation rate of follicular cells and decreased percentage of apoptotic cells that was more evident in the central than in the marginal region of the gland. Sex-related differences were also found, since the follicular epithelium height was higher in male than in female mice. The percentage of proliferating cells showed significant changes in male but not in female mice, and apoptotic cells were more abundant in female than in male IRS2-KO animals, without significant differences between WTanimals. Therefore, our results suggest that IRS2 could be involved in the maintenance of thyroid cells population and in the normal physiology of the thyroid gland.es_ES
dc.language.isoenges_ES
dc.publisherNature Researches_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectInsulin receptor substrate 2es_ES
dc.subjectThyroid glandes_ES
dc.subject.meshInsulin Receptor Substrate Proteins *
dc.subject.meshThyroid Gland *
dc.titleThe influence of the lack of insulin receptor substrate 2 (IRS2) on the thyroid glandes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1038/s41598-019-42198-7es_ES
dc.identifier.doi10.1038/s41598-019-42198-7
dc.relation.projectIDFIS–PI021803es_ES
dc.relation.projectIDFIS–PI030818es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn2045-2322
dc.journal.titleScientific Reportses_ES
dc.volume.number9es_ES
dc.issue.number1es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsproteínas sustrato del receptor de insulina *
dc.subject.decsglándula tiroides *
dc.description.projectInstituto de Salud Carlos IIIes_ES


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