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dc.contributor.authorAntequera, Desireé 
dc.contributor.authorCarrero, Laura
dc.contributor.authorCunha Alves, Victoria
dc.contributor.authorFerrer, Isidro
dc.contributor.authorHernández-Gallego, Jesús
dc.contributor.authorMunicio, Cristina
dc.contributor.authorCarro, Eva 
dc.date.accessioned2023-04-26T14:06:55Z
dc.date.available2023-04-26T14:06:55Z
dc.date.issued2022-07-08
dc.identifier.citationBiomedicines. 2022 Jul 8;10(7):1645.es_ES
dc.identifier.issn2227-9059es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/15901
dc.description.abstractImpaired brain clearance mechanisms may result in the accumulation of aberrant proteins that define Alzheimer's disease (AD). The water channel protein astrocytic aquaporin 4 (AQP4) is essential for brain amyloid-β clearance, but it is known to be abnormally expressed in AD brains. The expression of AQPs is differentially regulated during diverse brain injuries, but, whereas AQP4 expression and function have been studied in AD, less is known about AQP5. AQP5 functions include not only water transport but also cell migration mediated by cytoskeleton regulation. Moreover, AQP5 has been reported to be expressed in astrocytes, which are regulated after ischemic and traumatic injury. Additionally, AQP5 is particularly abundant in the salivary glands suggesting that it may be a crucial factor in gland dysfunction associated with AD. Herein, we aim to determine whether AQP5 expression in submandibular glands and the brain was altered in AD. First, we demonstrated impaired AQP5 expression in submandibular glands in APP/PS1 mice and AD patients. Subsequently, we observed that AQP5 expression was upregulated in APP/PS1 cerebral cortex and confirmed its expression both in astrocytes and neurons. Our findings propose AQP5 as a significant role player in AD pathology, in addition to AQP4, representing a potential target for the treatment of AD.es_ES
dc.description.sponsorshipThis study was supported by grants from Instituto de Salud Carlos III through the project PI2021/00679) and cofounded by the European Union, Hospital Universitario 12 de Octubre Research Institute (2022/0068), FEDER, Comunidad de Madrid (S2017/BMD-3700; NEUROMETAB-CM), and CIBERNED (CB07/502, PI2021/03).es_ES
dc.language.isoenges_ES
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI) es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectAlzheimer’s diseasees_ES
dc.subjectAquaporinses_ES
dc.subjectAstrocyteses_ES
dc.subjectNeuronses_ES
dc.subjectSubmandibular glandes_ES
dc.titleDifferentially Aquaporin 5 Expression in Submandibular Glands and Cerebral Cortex in Alzheimer's Diseasees_ES
dc.typejournal articlees_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID35884950es_ES
dc.format.volume10es_ES
dc.format.number7es_ES
dc.format.page1645es_ES
dc.identifier.doi10.3390/biomedicines10071645es_ES
dc.contributor.funderInstituto de Salud Carlos III es_ES
dc.contributor.funderResearch Institute Hospital 12 de Octubre es_ES
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF) es_ES
dc.contributor.funderComunidad de Madrid (España) es_ES
dc.contributor.funderCentro de Investigación Biomédica en Red - CIBERNED (Enfermedades Neurodegenerativas) es_ES
dc.description.peerreviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.3390/biomedicines10071645es_ES
dc.identifier.journalBiomedicineses_ES
dc.repisalud.centroISCIII::Unidad Funcional de Investigación de Enfermedades Crónicas (UFIEC)es_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.relation.projectFISinfo:fis/Instituto de Salud Carlos III///PI21 - Proyectos de investigacion en salud (AES 2021). Modalidad proyectos de investigación en salud. (2021)/PI21/00679es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/PI2021/03es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/CB07/502es_ES


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Atribución 4.0 Internacional
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