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dc.contributor.authorGarcía Macia, Marina 
dc.contributor.authorSantos Ledo, Adrián 
dc.contributor.authorCaballero, Beatriz
dc.contributor.authorRubio-González, Adrian
dc.contributor.authorde Luxán-Delgado, Beatriz
dc.contributor.authorPotes, Yaiza
dc.contributor.authorRodríguez-González, Susana Mª.
dc.contributor.authorBoga, José Antonio
dc.contributor.authorCoto-Montes, Ana
dc.date.accessioned2025-01-17T10:28:59Z
dc.date.available2025-01-17T10:28:59Z
dc.date.issued2019
dc.identifier.citationGarcía-Macia, M., Santos-Ledo, A., Caballero, B., Rubio-González, A., de Luxán-Delgado, B., Potes, Y., Rodríguez-González, S. Mª., Boga, J. A., & Coto-Montes, A. (2019). Selective autophagy, lipophagy and mitophagy, in the Harderian gland along the oestrous cycle: a potential retrieval effect of melatonin. Scientific Reports, 9(1). https://doi.org/10.1038/S41598-019-54743-5es_ES
dc.identifier.urihttp://hdl.handle.net/10366/161912
dc.description.abstract[EN]Sexual dimorphism has been reported in many processes. However, sexual bias in favour of the use of males is very present in science. One of the main reasons is that the impact of hormones in diverse pathways and processes such as autophagy have not been properly addressed in vivo. The Harderian gland is a perfect model to study autophagic modulation as it exhibits important changes during the oestrous cycle. The aim of this study is to identify the main processes behind Harderian gland differences under oestrous cycle and their modulator. In the present study we show that redox-sensitive transcription factors have an essential role: NF-κB may activate SQSTM1/p62 in oestrus, promoting selective types of autophagy: mitophagy and lipophagy. Nrf2 activation in dioestrus, leads the retrieval phase and restoration of mitochondrial homeostasis. Melatonin’s receptors show higher expression in dioestrus, leading to decreases in pro-inflammatory mediators and enhanced Nrf2 expression. Consequently, autophagy is blocked, and porphyrin release is reduced. All these results point to melatonin as one of the main modulators of the changes in autophagy during the oestrous cycle.es_ES
dc.description.sponsorshipWe are members of the INPROTEOLYS, SEBBM, SEFAGIA and INEUROPA network. We acknowledge Fibrosis and Bolaños´lab for their support during the manuscript revisions. This work was supported by FISS-18-PI17/02009, C0120R3166, C0245R4032 and BH182173. MG-M has a postdoctoral fellowship from the Instituto de Salud Carlos III (ISCIII), Ministerio de Ciencia, Innovación y Universidades. Financial support from the University of Oviedo is also acknowledged.es_ES
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMelatonines_ES
dc.subjectAutophagyes_ES
dc.subjectMousees_ES
dc.subjectLipophagyes_ES
dc.subjectSexual cyclees_ES
dc.subjectMitophagyes_ES
dc.subject.meshHarderian Gland *
dc.subject.meshMelatonin *
dc.subject.meshSexual Behavior, Animal *
dc.subject.meshReproduction *
dc.subject.meshRodentia *
dc.subject.meshAutophagy *
dc.titleSelective autophagy, lipophagy and mitophagy, in the Harderian gland along the oestrous cycle: a potential retrieval effect of melatonines_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/ 10.1038/S41598-019-54743-5es_ES
dc.subject.unesco2407 Biología Celulares_ES
dc.subject.unesco2401 Biología Animal (Zoología)es_ES
dc.subject.unesco2411.16 Fisiología de la Reproducciónes_ES
dc.identifier.doi10.1038/s41598-019-54743-5
dc.relation.projectIDFISS-18-PI17/02009es_ES
dc.relation.projectIDC0120R3166es_ES
dc.relation.projectIDC0245R4032es_ES
dc.relation.projectIDBH182173es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.pmid31819084
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.decsglándula de Harder *
dc.subject.decsreproducción *
dc.subject.decsRodentia *
dc.subject.decsautofagia *
dc.subject.decsconducta sexual animal *
dc.subject.decsmelatonina *


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