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dc.contributor.authorSot, Jesús
dc.contributor.authorGarcía Arribas, Aritz ORCID
dc.contributor.authorAbad García, Beatriz
dc.contributor.authorArranz, Sara
dc.contributor.authorPortune, Kevin
dc.contributor.authorAndrade, Fernando
dc.contributor.authorMartín Nieto, Alicia
dc.contributor.authorVelasco, Olaia
dc.contributor.authorArana, Eunate
dc.contributor.authorTueros, Itziar
dc.contributor.authorFerreri, Carla
dc.contributor.authorGaztambide Sáenz, María Sonia
dc.contributor.authorGoñi Urcelay, Félix María ORCID
dc.contributor.authorCastaño González, Luis Antonio ORCID
dc.contributor.authorAlonso Izquierdo, Alicia ORCID
dc.date.accessioned2022-02-16T18:25:53Z
dc.date.available2022-02-16T18:25:53Z
dc.date.issued2022-02-08
dc.identifier.citationInternational Journal of Molecular Sciences 23(3) : (2022) // Article ID 1920es_ES
dc.identifier.issn1422-0067
dc.identifier.urihttp://hdl.handle.net/10810/55492
dc.description.abstractThis work intends to describe the physical properties of red blood cell (RBC) membranes in obese adults. The hypothesis driving this research is that obesity, in addition to increasing the amount of body fat, will also modify the lipid composition of membranes in cells other than adipocytes. Forty-nine control volunteers (16 male, 33 female, BMI 21.8 ± 5.6 and 21.5 ± 4.2 kg/m2, respectively) and 52 obese subjects (16 male and 36 female, BMI 38.2± 11.0 and 40.7 ± 8.7 kg/m2, respectively) were examined. The two physical techniques applied were atomic force microscopy (AFM) in the force spectroscopy mode, which allows the micromechanical measurement of penetration forces, and fluorescence anisotropy of trimethylammonium diphenylhexatriene (TMA-DPH), which provides information on lipid order at the membrane polar–nonpolar interface. These techniques, in combination with lipidomic studies, revealed a decreased rigidity in the interfacial region of the RBC membranes of obese as compared to control patients, related to parallel changes in lipid composition. Lipidomic data show an increase in the cholesterol/phospholipid mole ratio and a decrease in sphingomyelin contents in obese membranes. ω-3 fatty acids (e.g., docosahexaenoic acid) appear to be less prevalent in obese patient RBCs, and this is the case for both the global fatty acid distribution and for the individual major lipids in the membrane phosphatidylcholine (PC), phosphatidylethanolamine (PE) and phosphatidylserine (PS). Moreover, some ω-6 fatty acids (e.g., arachidonic acid) are increased in obese patient RBCs. The switch from ω-3 to ω-6 lipids in obese subjects could be a major factor explaining the higher interfacial fluidity in obese patient RBC membranes.es_ES
dc.description.sponsorshipThis work was supported in part by the Basque Government Department of Economic Development, grant No. KK-2019/00028 (OBINTER); the Basque Government Department of Education, grants No. IT1264-19, IT1281-19, IT1270-19, and IT1625-22; the Basque Government Department of Health, grants No. 2019-222030, 2020-333023; Fundación Ramón Areces; and by Centre for the Development of Industrial Technology (CDTI) of the Spanish Ministry of Science and Innovation under the grant agreement: TECNOMIFOOD project (CER-20191010) and Basque Government: IT1625-22.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjectobesityes_ES
dc.subjectcell membrane physical propertieses_ES
dc.subjectmembrane fluidityes_ES
dc.subjectfluorescence polarizationes_ES
dc.subjectatomic force microscopyes_ES
dc.subjectmembrane breakthrough forcees_ES
dc.subjectlipidomicses_ES
dc.titleErythrocyte Membrane Nanomechanical Rigidity Is Decreased in Obese Patientses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2022-02-11T14:46:44Z
dc.rights.holder© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1422-0067/23/3/1920es_ES
dc.identifier.doi10.3390/ijms23031920
dc.departamentoesBioquímica y biología molecular
dc.departamentoesMedicina
dc.departamentoesPediatría
dc.departamentoeuBiokimika eta biologia molekularra
dc.departamentoeuMedikuntza
dc.departamentoeuPediatria


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© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).