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Oxidized LDL Increase the Proinflammatory Profile of Human Visceral Adipocytes Produced by Hypoxia

Background: Little is known about the effects of hypoxia on scavenger receptors (SRs) levels in adipocytes. We analyzed the effect of morbid obesity and hypoxia on SRs and inflammation markers in human visceral adipocytes and whether ox-LDL modify the inflammatory profile produced by hypoxia. Method...

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Autores principales: Santiago-Fernández, Concepción, Martín-Reyes, Flores, Tome, Monica, Gutierrez-Repiso, Carolina, Fernandez-Garcia, Diego, Ocaña-Wilhelmi, Luis, Rivas-Becerra, Jose, Tatzber, Franz, Pursch, Edith, Tinahones, Francisco J., García-Fuentes, Eduardo, Garrido-Sánchez, Lourdes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8615639/
https://www.ncbi.nlm.nih.gov/pubmed/34829944
http://dx.doi.org/10.3390/biomedicines9111715
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author Santiago-Fernández, Concepción
Martín-Reyes, Flores
Tome, Monica
Gutierrez-Repiso, Carolina
Fernandez-Garcia, Diego
Ocaña-Wilhelmi, Luis
Rivas-Becerra, Jose
Tatzber, Franz
Pursch, Edith
Tinahones, Francisco J.
García-Fuentes, Eduardo
Garrido-Sánchez, Lourdes
author_facet Santiago-Fernández, Concepción
Martín-Reyes, Flores
Tome, Monica
Gutierrez-Repiso, Carolina
Fernandez-Garcia, Diego
Ocaña-Wilhelmi, Luis
Rivas-Becerra, Jose
Tatzber, Franz
Pursch, Edith
Tinahones, Francisco J.
García-Fuentes, Eduardo
Garrido-Sánchez, Lourdes
author_sort Santiago-Fernández, Concepción
collection PubMed
description Background: Little is known about the effects of hypoxia on scavenger receptors (SRs) levels in adipocytes. We analyzed the effect of morbid obesity and hypoxia on SRs and inflammation markers in human visceral adipocytes and whether ox-LDL modify the inflammatory profile produced by hypoxia. Methods: We studied in 17 non-obese and 20 subjects with morbid obesity (MO) the mRNA expression of HIF-1α, SRs (LOX-1, MSR1, CL-P1 and CXCL16), IL6 and TNFα in visceral adipocytes and the effect of hypoxia with or without ox-LDL on visceral in vitro-differentiated adipocytes (VDA). Results: HIF-1α, TNFα, IL6, LOX-1, MSR1 and CXCL16 expression in adipocytes was increased in MO when compared with those in non-obese subjects (p < 0.05). The expression of most of the inflammatory markers and SRs gene correlated with HIF-1α. In VDA, hypoxia increased TNFα, IL6, MSR1, CXCL16 and CL-P1 (p < 0.05) in non-obese subjects, and TNFα, IL6, MSR1 and CXCL16 (p < 0.05) in MO. Silencing HIF-1α prevented the increase of TNFα, IL6, LOX-1, MSR1, CL-P1 and CXCL16 expression (p < 0.05). The combination of hypoxia and ox-LDL produced higher TNFα expression (p = 0.041). Conclusions: Morbid obesity and hypoxia increased SRs and inflammatory markers in visceral adipocytes. In a hypoxic state, ox-LDL increased the proinflammatory response of visceral adipocytes to hypoxia.
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spelling pubmed-86156392021-11-26 Oxidized LDL Increase the Proinflammatory Profile of Human Visceral Adipocytes Produced by Hypoxia Santiago-Fernández, Concepción Martín-Reyes, Flores Tome, Monica Gutierrez-Repiso, Carolina Fernandez-Garcia, Diego Ocaña-Wilhelmi, Luis Rivas-Becerra, Jose Tatzber, Franz Pursch, Edith Tinahones, Francisco J. García-Fuentes, Eduardo Garrido-Sánchez, Lourdes Biomedicines Article Background: Little is known about the effects of hypoxia on scavenger receptors (SRs) levels in adipocytes. We analyzed the effect of morbid obesity and hypoxia on SRs and inflammation markers in human visceral adipocytes and whether ox-LDL modify the inflammatory profile produced by hypoxia. Methods: We studied in 17 non-obese and 20 subjects with morbid obesity (MO) the mRNA expression of HIF-1α, SRs (LOX-1, MSR1, CL-P1 and CXCL16), IL6 and TNFα in visceral adipocytes and the effect of hypoxia with or without ox-LDL on visceral in vitro-differentiated adipocytes (VDA). Results: HIF-1α, TNFα, IL6, LOX-1, MSR1 and CXCL16 expression in adipocytes was increased in MO when compared with those in non-obese subjects (p < 0.05). The expression of most of the inflammatory markers and SRs gene correlated with HIF-1α. In VDA, hypoxia increased TNFα, IL6, MSR1, CXCL16 and CL-P1 (p < 0.05) in non-obese subjects, and TNFα, IL6, MSR1 and CXCL16 (p < 0.05) in MO. Silencing HIF-1α prevented the increase of TNFα, IL6, LOX-1, MSR1, CL-P1 and CXCL16 expression (p < 0.05). The combination of hypoxia and ox-LDL produced higher TNFα expression (p = 0.041). Conclusions: Morbid obesity and hypoxia increased SRs and inflammatory markers in visceral adipocytes. In a hypoxic state, ox-LDL increased the proinflammatory response of visceral adipocytes to hypoxia. MDPI 2021-11-18 /pmc/articles/PMC8615639/ /pubmed/34829944 http://dx.doi.org/10.3390/biomedicines9111715 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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/).
spellingShingle Article
Santiago-Fernández, Concepción
Martín-Reyes, Flores
Tome, Monica
Gutierrez-Repiso, Carolina
Fernandez-Garcia, Diego
Ocaña-Wilhelmi, Luis
Rivas-Becerra, Jose
Tatzber, Franz
Pursch, Edith
Tinahones, Francisco J.
García-Fuentes, Eduardo
Garrido-Sánchez, Lourdes
Oxidized LDL Increase the Proinflammatory Profile of Human Visceral Adipocytes Produced by Hypoxia
title Oxidized LDL Increase the Proinflammatory Profile of Human Visceral Adipocytes Produced by Hypoxia
title_full Oxidized LDL Increase the Proinflammatory Profile of Human Visceral Adipocytes Produced by Hypoxia
title_fullStr Oxidized LDL Increase the Proinflammatory Profile of Human Visceral Adipocytes Produced by Hypoxia
title_full_unstemmed Oxidized LDL Increase the Proinflammatory Profile of Human Visceral Adipocytes Produced by Hypoxia
title_short Oxidized LDL Increase the Proinflammatory Profile of Human Visceral Adipocytes Produced by Hypoxia
title_sort oxidized ldl increase the proinflammatory profile of human visceral adipocytes produced by hypoxia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8615639/
https://www.ncbi.nlm.nih.gov/pubmed/34829944
http://dx.doi.org/10.3390/biomedicines9111715
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