Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/108735
DC FieldValueLanguage
dc.contributor.authorRodrigues, Lisa-
dc.contributor.authorMiranda, Isabel M.-
dc.contributor.authorAndrade, Geanne M.-
dc.contributor.authorMota, Marta-
dc.contributor.authorCortes, Luísa-
dc.contributor.authorRodrigues, Acácio G.-
dc.contributor.authorCunha, Rodrigo A.-
dc.contributor.authorGonçalves, Teresa-
dc.date.accessioned2023-09-11T10:50:02Z-
dc.date.available2023-09-11T10:50:02Z-
dc.date.issued2016-09-27-
dc.identifier.issn1949-2553pt
dc.identifier.urihttps://hdl.handle.net/10316/108735-
dc.description.abstractOpportunistic gut infections and chronic inflammation, in particular due to overgrowth of Candida albicans present in the gut microbiota, are increasingly reported in the elder population. In aged, adult and young mice, we now compared the relative intestinal over-colonization by ingested C. albicans and their translocation to other organs, focusing on the role of adenosine A2A receptors that are a main stop signal of inflammation. We report that elderly mice are more prone to over-colonization by C. albicans than adult and young mice. This fungal over-growth seems to be related with higher growth rate in intestinal lumen, independent of gut tissues invasion, but resulting in higher GI tract inflammation. We observed a particularly high colonization of the stomach, with increased rate of yeast-to-hypha transition in aged mice. We found a correlation between A2A receptor density and tissue damage due to yeast infection: comparing with young and adults, aged mice have a lower gut A2A receptor density and C. albicans infection failed to increase it. In conclusion, this study shows that aged mice have a lower ability to cope with inflammation due to C. albicans over-colonization, associated with an inability to adaptively adjust adenosine A2A receptors density.pt
dc.description.sponsorshipThis work was supported by Fundação para a Ciência e Tecnologia (FCT) grants (PTDC/SAUFCF/ 81436/2006; PTDC/SAU-MIC/115598/2009), by FEDER funds through the Operational Programme Competitiveness Factors - COMPETE and national funds by FCT -Foundation for Science and Technology under the strategic project UID/ NEU / 04539 / 2013 and also by NARSAD. LR is a recipient of a PhD grant by FCT (SFRH/BD/74181/2010). IMM is supported by FCT (BPD/113285/2015), FEDER and COMPETE.pt
dc.language.isoengpt
dc.publisherImpact Journalspt
dc.relationPTDC/SAU-MIC/115598/2009pt
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID/NEU/04539/2013pt
dc.relationSFRH/BD/74181/2010pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectageingpt
dc.subjectinfectionpt
dc.subjectgutpt
dc.subjectCandida albicanspt
dc.subjectadenosine A2A receptorspt
dc.subjectGerotargetpt
dc.subject.meshAnimalspt
dc.subject.meshCandidiasispt
dc.subject.meshFecespt
dc.subject.meshGastrointestinal Tractpt
dc.subject.meshInflammationpt
dc.subject.meshMalept
dc.subject.meshMicept
dc.subject.meshMice, Inbred C57BLpt
dc.subject.meshReceptor, Adenosine A2Apt
dc.subject.meshStomachpt
dc.subject.meshAgingpt
dc.subject.meshCandida albicanspt
dc.titleBlunted dynamics of adenosine A2A receptors is associated with increased susceptibility to Candida albicans infection in the elderlypt
dc.typearticle-
degois.publication.firstPage62862pt
degois.publication.lastPage62872pt
degois.publication.issue39pt
degois.publication.titleOncotargetpt
dc.peerreviewedyespt
dc.identifier.doi10.18632/oncotarget.11760pt
degois.publication.volume7pt
dc.date.embargo2016-09-27*
uc.date.periodoEmbargo0pt
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.project.grantnoCNC. IBILI-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0001-9898-2409-
crisitem.author.orcid0000-0001-9363-4130-
crisitem.author.orcid0000-0003-2550-6422-
crisitem.author.orcid0000-0001-9347-0535-
Appears in Collections:I&D CNC - Artigos em Revistas Internacionais
FMUC Medicina - Artigos em Revistas Internacionais
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