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dc.contributor.authorCoto-Montes, Ana
dc.contributor.authorGarcía Macia, Marina 
dc.contributor.authorCaballero, Beatriz
dc.contributor.authorSierra, Verónica
dc.contributor.authorRodríguez-Colunga, María J
dc.contributor.authorReiter, Russel J
dc.contributor.authorVega-Naredo, Ignacio
dc.date.accessioned2025-12-10T18:04:37Z
dc.date.available2025-12-10T18:04:37Z
dc.date.issued2013-05
dc.identifier.citationCoto‐Montes, A., García‐Macía, M., Caballero, B., Sierra, V., Rodríguez‐Colunga, M. J., Reiter, R. J., & Vega‐Naredo, I. (2013). Analysis of constant tissue remodeling in Syrian hamster Harderian gland: intra‐tubular and inter‐tubular syncytial masses. Journal of anatomy, 222(5), 558-569.es_ES
dc.identifier.issn0021-8782
dc.identifier.urihttp://hdl.handle.net/10366/168202
dc.description.abstract[EN]The Syrian hamster Harderian gland (HG) has a marked sexual dimorphism and exhibits an extraordinary rate of porphyrinogenesis. The physiological oxidative stress, derived from constant porphyrin production, is so high that the HG needs additional survival autophagic mechanisms to fight against this chronic exposure, provoking the triggering of a holocrine secretion in female glands that forms two types of secretory masses: intra-tubular-syncytial and inter-tubular-syncytial masses. The aim of this work was to study the development of this inter-tubular holocrine secretion. To approach this task, we have considered that the steps developed during the formation of the so-called invasive masses consist of the growth of epithelial cells, cell detachment from the basal lamina and invasion of surrounding tissues. The presence of these masses, particularly in the female HG, are closely linked to sexual dimorphism in redox balance and to alterations in the expression of certain factors such as cytokeratins, P-cadherin, matrix metalloproteinases, cathepsin H, proliferating cell nuclear antigen, p53, CD-31 and vascular endothelial growth factor, which seem to be involved in tissue remodeling. The results document unusual mechanisms of secretion in Syrian hamster HG: an extraordinary system of massive secretion through the conjunctive tissue, disrupting the branched structure of the gland.es_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectcell detachmentes_ES
dc.subjectextracellular matrixes_ES
dc.subjectHarderian glandes_ES
dc.subjectinvasive secretiones_ES
dc.subjectoxidative stresses_ES
dc.subject.meshHarderian Gland *
dc.subject.meshOxidative Stress *
dc.subject.meshSex Characteristics *
dc.subject.meshImmunohistochemistry *
dc.subject.meshAnimals *
dc.subject.meshMesocricetus *
dc.subject.meshCricetinae *
dc.subject.meshLipid Peroxidation *
dc.subject.meshCadherins *
dc.subject.meshCathepsin H *
dc.subject.meshKeratins *
dc.subject.meshAutophagy *
dc.titleAnalysis of constant tissue remodeling in Syrian hamster Harderian gland: intra-tubular and inter-tubular syncytial masseses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1111/joa.12040es_ES
dc.identifier.doi10.1111/joa.12040
dc.relation.projectIDAGL2010-21578-C03-02es_ES
dc.relation.projectIDMICINN-10-BFU2010-20919es_ES
dc.relation.projectIDPIEF-GA-2009-251850es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/embargoedAccesses_ES
dc.audience.educationLevel
dc.audience.educationLevel
dc.identifier.pmid23496762
dc.identifier.essn1469-7580
dc.journal.titleJournal of Anatomyes_ES
dc.volume.number222es_ES
dc.issue.number5es_ES
dc.page.initial558es_ES
dc.page.final569es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsglándula de Harder *
dc.subject.decsinmunohistoquímica *
dc.subject.decsanimales *
dc.subject.decscatepsina H *
dc.subject.decsestrés oxidativo *
dc.subject.decsMesocricetus *
dc.subject.decsautofagia *
dc.subject.decsCricetinae *
dc.subject.decsqueratinas *
dc.subject.decscaracterísticas sexuales *
dc.subject.decsperoxidación de lípidos *
dc.subject.decscadherinas *


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