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Protein Carbamylation: A Marker Reflecting Increased Age-Related Cell Oxidation

dc.contributor.authorCarracedo Añón, Julia María
dc.contributor.authorRamírez-Carracedo, Rafael
dc.contributor.authorMartínez de Toda, Irene
dc.contributor.authorVida Rueda, Carmen
dc.contributor.authorAlique, Matilde
dc.contributor.authorFuente del Rey, Mónica de la
dc.contributor.authorRamírez-Chamond, Rafael
dc.date.accessioned2023-06-17T12:33:33Z
dc.date.available2023-06-17T12:33:33Z
dc.date.issued2018-05-17
dc.description.abstractCarbamylation is a post-translational modification of proteins that may partake in the oxidative stress-associated cell damage, and its increment has been recently proposed as a “hallmark of aging”. The molecular mechanisms associated with aging are related to an increased release of free radicals. We have studied whether carbamylated proteins from the peripheral blood of healthy subjects are related to oxidative damage and aging, taking into account the gender and the immune profile of the subjects. The study was performed in healthy human volunteers. The detection of protein carbamylation and malondialdehyde (MDA) levels was evaluated using commercial kits. The immune profile was calculated using parameters of immune cell function. The results show that the individuals from the elderly group (60–79 years old) have increased carbamylated protein and MDA levels. When considered by gender, only men between 60 and 79 years old showed significantly increased carbamylated proteins and MDA levels. When those subjects were classified by their immune profile, the carbamylated protein levels were higher in those with an older immune profile. In conclusion, the carbamylation of proteins in peripheral blood is related to age-associated oxidative damage and to an aging functional immunological signature. Our results suggest that carbamylated proteins may play an important role at the cellular level in the aging process.
dc.description.departmentDepto. de Genética, Fisiología y Microbiología
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipInstituto de Salud Carlos III (ISCIII)/FEDER
dc.description.sponsorshipJunta de Andalucía
dc.description.sponsorshipUniversidad Complutense de Madrid/Banco de Santander
dc.description.sponsorshipRed de Investigación Renal (REDinREN)
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/64393
dc.identifier.doi10.3390/ijms19051495
dc.identifier.issn1422-0067
dc.identifier.officialurlhttps://doi.org/10.3390/ijms19051495
dc.identifier.relatedurlhttps://www.mdpi.com/1422-0067/19/5/1495
dc.identifier.urihttps://hdl.handle.net/20.500.14352/12489
dc.issue.number5
dc.journal.titleInternational Journal of Molecular Sciences
dc.language.isoeng
dc.page.initial1495
dc.publisherMDPI
dc.relation.projectID(PI14/00806, PI15/01787, PI17/01029)
dc.relation.projectID(P12-CTS-7352)
dc.relation.projectID(PR41/17-20964)
dc.relation.projectID(REDinREN; RD16/0009/0034)
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.cdu577.27
dc.subject.keywordaging biomarker
dc.subject.keywordfunctional immune signature
dc.subject.keywordimmune profile
dc.subject.keywordlipid peroxidation
dc.subject.keywordmalondialdehyde
dc.subject.keywordoxidative damage
dc.subject.keywordprotein carbamylation
dc.subject.ucmInmunología
dc.subject.ucmBiología celular (Biología)
dc.subject.unesco2412 Inmunología
dc.subject.unesco2407 Biología Celular
dc.titleProtein Carbamylation: A Marker Reflecting Increased Age-Related Cell Oxidation
dc.typejournal article
dc.volume.number19
dspace.entity.typePublication
relation.isAuthorOfPublication447f8cb2-a0b7-4398-9c77-baff3dd853e7
relation.isAuthorOfPublication.latestForDiscovery447f8cb2-a0b7-4398-9c77-baff3dd853e7

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