Afficher la notice abrégée

dc.contributor.authorFernández Dolón, Jorge
dc.contributor.authorPaniagua, Antonio E.
dc.contributor.authorValle, Vicente
dc.contributor.authorSegurado Gelado, Alicia 
dc.contributor.authorArévalo Arévalo, María Rosario 
dc.contributor.authorVelasco Arranz, María Almudena 
dc.contributor.authorLillo Delgado, María Concepción 
dc.date.accessioned2024-02-01T09:58:29Z
dc.date.available2024-02-01T09:58:29Z
dc.date.issued2018
dc.identifier.urihttp://hdl.handle.net/10366/155145
dc.description.abstractAcquisition of cell polarization is essential for the performance of crucial functions, like a successful secretion and appropriate cell signaling in many tissues, and it depends on the correct functioning of polarity proteins, including the Crumbs complex. The CRB proteins, CRB1, CRB2 and CRB3, identified in mammals, are expressed in epithelial-derived tissues like brain, kidney and retina. CRB2 has a ubiquitous expression and has been detected in embryonic brain tissue; but currently there is no data regarding its localization in the adult brain. In our study, we characterized the presence of CRB2 in adult mice brain, where it is particularly enriched in cortex, hippocampus, hypothalamus and cerebellum. Double immunofluorescence analysis confirmed that CRB2 is a neuron-specific protein, present in both soma and projections where colocalizes with certain populations of exocytic and endocytic vesicles and with other members of the Crumbs complex. Finally, in the cortex of CRB1rd8 mutant mice that contain a mutation in the Crb1 gene generating a truncated CRB1 protein, there is an abnormal increase in the expression levels of the CRB2 protein which suggests a possible compensatory mechanism for the malfunction of CRB1 in this mutant background.es_ES
dc.description.sponsorshipThis study was supported by Fondo de Investigaciones Sanitarias Instituto Carlos III (PI15/01240), co-funded by European Union (ERDF/ESF, “Investing in your future”) to C.L. A. Velasco, R. Arévalo and C. Lillo are members of the UIC.077 from Junta de Castilla y León.es_ES
dc.format.mimetypeapplicatio/pdf
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCRB2es_ES
dc.subjectCRB1rd8es_ES
dc.subjectCrumbs complexes_ES
dc.subjectmouse braines_ES
dc.subjectCRB1rd8 mutant micees_ES
dc.subject.meshMice, Neurologic Mutants *
dc.subject.meshCerebrum *
dc.titleExpression and localization of the polarity protein CRB2 in adult mouse brain: a comparison with the CRB1rd8 mutant mouse modeles_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://www.nature.com/articles/s41598-018-30210-5es_ES
dc.subject.unesco2490 Neurocienciases_ES
dc.identifier.doi10.1038/S41598-018-30210-5
dc.relation.projectIDPI15/01240es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn2045-2322
dc.journal.titleScientific Reportses_ES
dc.volume.number8es_ES
dc.issue.number1es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decscerebro *
dc.subject.decsratones mutantes neurológicos *


Fichier(s) constituant ce document

Thumbnail

Ce document figure dans la(les) collection(s) suivante(s)

Afficher la notice abrégée

Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Excepté là où spécifié autrement, la license de ce document est décrite en tant que Attribution-NonCommercial-NoDerivatives 4.0 Internacional