Mostrar el registro sencillo del ítem

dc.contributor.authorCatalano Iniesta, Leonardo 
dc.contributor.authorSánchez-Robledo, Virginia
dc.contributor.authorIglesias Osma, María Carmen 
dc.contributor.authorGalán Albiñana, Amparo
dc.contributor.authorCarrero García, Sixto 
dc.contributor.authorBlanco Barco, Enrique José 
dc.contributor.authorCarretero Hernández, Marta
dc.contributor.authorCarretero González, José 
dc.contributor.authorGarcía-Barrado, Maria Jose
dc.date.accessioned2025-12-19T10:09:09Z
dc.date.available2025-12-19T10:09:09Z
dc.date.issued2020-02-13
dc.identifier.citationCatalano‐Iniesta, L., Robledo, V. S., Iglesias‐Osma, M. C., Albiñana, A. G., Carrero, S., Blanco, E. J., Carretero‐Hernández, M., Carretero, J., & García‐Barrado, M. J. (2020). Evidences for expression and location of ANGPTL8 in human adipose tissue. Journal of Clinical Medicine, 9(2). https://doi.org/10.3390/JCM9020512es_ES
dc.identifier.urihttp://hdl.handle.net/10366/168418
dc.description.abstract[EN]The metabolism of triglycerides (TGs) is regulated, among others, by the lipoprotein lipase (LPL) that hydrolyses the TGs on endothelial cells. In turn, LPL is inhibited by the ANGPTLs family of proteins, such as ANGPTL3, 4, and, 8; the latter is the least known. In this work, we have tried to establish the expression and localisation of the Angiopoietin-like 8 (ANGPTL8) protein in the visceral adipose tissue (VAT) of morbid-obese and non-obese patients. 109 subjects (66 women and 43 men) undergoing laparoscopic surgery participated in this study. A blood sample and a portion of the VAT were obtained, and the patients were classified according to their Body Mass Index (BMI) as non-obese (19.5–30 kg/m2) and morbid-obese (40–50 kg/m2). No significant changes in ANGPTL8 plasma levels were determined by EIA in obese patients. The immunocytochemistry and Western blotting showed the presence of increased ANGPTL8 in morbid-obese patients (p < 0.05). In-situ hybridisation and a real time polymerase chain reaction (RT-PCR) confirmed that the mRNA that encodes ANGPTL8 was present in adipocytes, without differences in their nutritional state (p = 0.89), and even in the endothelial cells. Our data suggests that ANGPT8 plasmatic levels do not change significantly in patients with morbid obesity, although there is a modest difference related to gender. Besides, we demonstrate that in visceral adipose tissue, ANGPTL8 is well defined in the cytoplasm of adipocytes coexisting with perilipin-1 and its mRNA, also is present in endothelial cells. These findings suggest the possibility that among other functions, ANGPTL8 could perform either a paracrine and/or an endocrine role in the adipose tissue.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectANGPTL8es_ES
dc.subjectVisceral adipose tissuees_ES
dc.subjectObesityes_ES
dc.subjectEndothelial cellses_ES
dc.subject.meshAdipose Tissue, White *
dc.subject.meshEndothelial Cells *
dc.subject.meshObesity *
dc.titleEvidences for expression and location of ANGPTL8 in human adipose tissuees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.3390/jcm9020512es_ES
dc.identifier.doi10.3390/jcm9020512
dc.relation.projectIDBIO/SA49/14es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn2077-0383
dc.journal.titleJournal of Clinical Medicinees_ES
dc.volume.number9es_ES
dc.issue.number2es_ES
dc.page.initial512es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decstejido adiposo blanco *
dc.subject.decsobesidad *
dc.subject.decscélulas endoteliales *
dc.description.projectGerencia Regional de Salud, Junta de Castilla y León y Universidad de Salamancaes_ES


Ficheros en el ítem

Thumbnail

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem

Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution-NonCommercial-NoDerivatives 4.0 Internacional