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dc.contributor.authorQueipo-Ortuño, María Isabel 
dc.contributor.authorEscoté Miró, Xavier
dc.contributor.authorCeperuelo-Mallafré, Victoria
dc.contributor.authorGarrido-Sánchez, Lourdes
dc.contributor.authorMiranda, Merce
dc.contributor.authorClemente-Postigo, María Mercedes 
dc.contributor.authorPérez-Pérez, Rafael
dc.contributor.authorPeral Fuentes, Belén
dc.contributor.authorCardona-Díaz, Fernando 
dc.contributor.authorFernández Real, José M
dc.contributor.authorTinahones-Madueño, Francisco José 
dc.contributor.authorVendrell Ortega, Joan
dc.date.accessioned2024-10-01T07:25:26Z
dc.date.available2024-10-01T07:25:26Z
dc.date.issued2012
dc.identifier.citationQueipo-Ortuño MI, Escoté X, Ceperuelo-Mallafré V, Garrido-Sanchez L, Miranda M, Clemente-Postigo M, et al. (2012) FABP4 Dynamics in Obesity: Discrepancies in Adipose Tissue and Liver Expression Regarding Circulating Plasma Levels. PLoS ONE 7(11): e48605. https://doi.org/10.1371/journal.pone.0048605es_ES
dc.identifier.urihttps://hdl.handle.net/10630/34102
dc.description.abstractBackground FABP4 is predominantly expressed in adipose tissue, and its circulating levels are linked with obesity and a poor atherogenic profile. Objective In patients with a wide BMI range, we analyze FABP4 expression in adipose and hepatic tissues in the settings of obesity and insulin resistance. Associations between FABP4 expression in adipose tissue and the FABP4 plasma level as well as the main adipogenic and lipolytic genes expressed in adipose tissue were also analyzed. Methods The expression of several lipogenic, lipolytic, PPAR family and FABP family genes was analyzed by real time PCR. FABP4 protein expression in total adipose tissues and its fractions were determined by western blot. Results In obesity FABP4 expression was down-regulated (at both mRNA and protein levels), with its levels mainly predicted by ATGL and inversely by the HOMA-IR index. The BMI appeared as the only determinant of the FABP4 variation in both adipose tissue depots. FABP4 plasma levels showed a significant progressive increase according to BMI but no association was detected between FABP4 circulating levels and SAT or VAT FABP4 gene expression. The gene expression of FABP1, FABP4 and FABP5 in hepatic tissue was significantly higher in tissue from the obese IR patients compared to the non-IR group. Conclusion The inverse pattern in FABP4 expression between adipose and hepatic tissue observed in morbid obese patients, regarding the IR context, suggests that both tissues may act in a balanced manner. These differences may help us to understand the discrepancies between circulating plasma levels and adipose tissue expression in obesity.es_ES
dc.description.sponsorshipThis work was supported by Fondo de Investigacion Sanitaria (FIS) 07/1024, 08/1195, CB06/03/0018, CP07/0095 and PI081655, 10/00967, 11/00085 from the Spanish Instituto de Salud Carlos III (ISCIII), Ministerio de Sanidad y Consumo; with the participation of the European Regional Development Fund (ERDF) SAF-2009-10461 from the Ministerio de Economia y Competitividad (MICINN), the Servicio Andaluz de Salud (PI325/2008) and Fundación Mutua Madrileña, Spain (BP). LGS and VCM are supported by fellowships from the Juan de la Cierva programme (JdlC) (JCI200904086 and JCI-2010-06395). CIBERs are an ISCIII Project. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.es_ES
dc.language.isoenges_ES
dc.publisherPLOS (Public Library of Science)es_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectObesidades_ES
dc.subjectPlasma sanguíneoes_ES
dc.subject.otherObesityes_ES
dc.subject.otherAdipose tissuees_ES
dc.subject.otherFABP4es_ES
dc.titleFABP4 Dynamics in Obesity: Discrepancies in Adipose Tissue and Liver Expression Regarding Circulating Plasma Levelses_ES
dc.typejournal articlees_ES
dc.centroFacultad de Cienciases_ES
dc.identifier.doi10.1371/journal.pone.0048605
dc.type.hasVersionVoRes_ES
dc.departamentoBiología Celular, Genética y Fisiología
dc.rights.accessRightsopen accesses_ES


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