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dc.contributor.authorTurpin, C.
dc.contributor.authorCatan, A.
dc.contributor.authorGuerin-Dubourg, A.
dc.contributor.authorDebussche, X.
dc.contributor.authorBravo López, Susana Belén
dc.contributor.authorAlvarez Castro, Ezequiel
dc.contributor.authorVan Den Elsen, J.
dc.contributor.authorMeilhac, O.
dc.contributor.authorRondeau, P.
dc.contributor.authorBourdon, E.
dc.date.accessioned2022-04-26T07:45:05Z
dc.date.available2022-04-26T07:45:05Z
dc.date.issued2020
dc.identifier.issn1932-6203
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/32628695es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16562
dc.description.abstractDiabetes is associated with a dramatic mortality rate due to its vascular complications. Chronic hyperglycemia in diabetes leads to enhanced glycation of erythrocytes and oxidative stress. Even though erythrocytes play a determining role in vascular complications, very little is known about how erythrocyte structure and functionality can be affected by glycation. Our objective was to decipher the impact of glycation on erythrocyte structure, oxidative stress parameters and capacity to interact with cultured human endothelial cells. In vitro glycated erythrocytes were prepared following incubation in the presence of different concentrations of glucose. To get insight into the in vivo relevance of our results, we compared these data to those obtained using red blood cells purified from diabetics or non-diabetics. We measured erythrocyte deformability, susceptibility to hemolysis, reactive oxygen species production and oxidative damage accumulation. Altered structures, redox status and oxidative modifications were increased in glycated erythrocytes. These modifications were associated with reduced antioxidant defence mediated by enzymatic activity. Enhanced erythrocyte phagocytosis by endothelial cells was observed when cultured with glycated erythrocytes, which was associated with increased levels of phosphatidylserine-likely as a result of an eryptosis phenomenon triggered by the hyperglycemic treatment. Most types of oxidative damage identified in in vitro glycated erythrocytes were also observed in red blood cells isolated from diabetics. These results bring new insights into the impact of glycation on erythrocyte structure, oxidative damage and their capacity to interact with endothelial cells, with a possible relevance to diabetes.en
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshCell Line*
dc.subject.meshHumans*
dc.subject.meshErythrocytes*
dc.subject.meshBlood Glucose*
dc.subject.meshHealthy Volunteers*
dc.subject.meshPrimary Cell Culture*
dc.subject.meshDiabetes Mellitus*
dc.subject.meshHemolysis*
dc.subject.meshCoculture Techniques*
dc.subject.meshReactive Oxygen Species*
dc.subject.meshErythrocyte Deformability*
dc.subject.meshOxidative Stress*
dc.subject.meshEndothelial Cells*
dc.titleEnhanced oxidative stress and damage in glycated erythrocytesen
dc.typeJournal Articlees
dc.authorsophosTurpin, C.;Catan, A.;Guerin-Dubourg, A.;Debussche, X.;Bravo, S. B.;Álvarez, E.;Van Den Elsen, J.;Meilhac, O.;Rondeau, P.;Bourdon, E.
dc.identifier.doi10.1371/journal.pone.0235335
dc.identifier.pmid32628695
dc.identifier.sophos39421
dc.issue.number7es
dc.journal.titlePLoS Onees
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS)es
dc.page.initiale0235335es
dc.rights.accessRightsopenAccess
dc.subject.decsespecies reactivas de oxígeno*
dc.subject.decseritrocitos*
dc.subject.decstécnicas de cocultivo*
dc.subject.decsdeformabilidad de los eritrocitos*
dc.subject.decsvoluntarios sanos*
dc.subject.decscultivo celular primario*
dc.subject.decslínea celular*
dc.subject.decsglucosa sanguínea*
dc.subject.decshumanos*
dc.subject.decsestrés oxidativo*
dc.subject.decshemólisis*
dc.subject.decsdiabetes mellitus*
dc.subject.decscélulas endoteliales*
dc.subject.keywordIDISes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number15es


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Atribución 4.0 Internacional
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