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Conjugated linoleic acid induces an atheroprotective macrophage MΦ2 phenotype and limits foam cell formation
BACKGROUND: Atherosclerosis, the underlying cause of heart attack and strokes, is a progresive dyslipidemic and inflammatory disease where monocyte-derived macrophage cells play a pivotal role. Although most of the mechanisms that contribute to the progression of atherosclerosis have been identified...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4340802/ https://www.ncbi.nlm.nih.gov/pubmed/25722654 http://dx.doi.org/10.1186/s12950-015-0060-9 |
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author | de Gaetano, Monica Alghamdi, Kawthar Marcone, Simone Belton, Orina |
author_facet | de Gaetano, Monica Alghamdi, Kawthar Marcone, Simone Belton, Orina |
author_sort | de Gaetano, Monica |
collection | PubMed |
description | BACKGROUND: Atherosclerosis, the underlying cause of heart attack and strokes, is a progresive dyslipidemic and inflammatory disease where monocyte-derived macrophage cells play a pivotal role. Although most of the mechanisms that contribute to the progression of atherosclerosis have been identified, there is limited information on those governing regression. Conjugated linoleic acid (CLA) is a group of isomers of linoleic acid that differ in the position and/or geometry of their double bonds. We have previously shown that a specific CLA blend (80:20 cis-9,trans-11:trans-10,cis-12-CLA) induces regression of pre-established atherosclerosis in vivo, via modulation of monocyte/macrophage function. However, the exact mechanisms through which CLA mediates this effect remain to be elucidated. METHODS: Here, we address if CLA primes monocytes towards an anti-inflammatory MΦ2 macrophage and examine the effect of individual CLA isomers and the atheroprotective blend on monocyte-macrophage differentiation, cytokine generation, foam cell formation and cholesterol metabolism in human peripheral blood monocyte (HPBMC)-derived macrophages. RESULTS: cis-9,trans-11-CLA and the atheroprotective 80:20 CLA blend regulates expression of pro-inflammatory mediators and modulates the inflammatory cytokine profile of macrophages and foam cells. In addition, cis-9,trans-11-CLA and CLA blend primes HPBMCs towards an anti-inflammatory MΦ2 phenotype, characterised by increased scavenger receptor (CD36) and efflux protein (ABCA-1) expression. Furthermore, this altered macrophage phenotype impacts on foam cell formation, inhibiting ox-LDL accumulation and promoting cholesterol efflux via both PPARγ and LXRα dependent pathways. CONCLUSION: The data increases the understanding of the pathways regulated by CLA in atheroprotection, namely, inhibiting the progressive acquisition of a pro-inflammatory macrophage phenotype. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12950-015-0060-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4340802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43408022015-02-27 Conjugated linoleic acid induces an atheroprotective macrophage MΦ2 phenotype and limits foam cell formation de Gaetano, Monica Alghamdi, Kawthar Marcone, Simone Belton, Orina J Inflamm (Lond) Research BACKGROUND: Atherosclerosis, the underlying cause of heart attack and strokes, is a progresive dyslipidemic and inflammatory disease where monocyte-derived macrophage cells play a pivotal role. Although most of the mechanisms that contribute to the progression of atherosclerosis have been identified, there is limited information on those governing regression. Conjugated linoleic acid (CLA) is a group of isomers of linoleic acid that differ in the position and/or geometry of their double bonds. We have previously shown that a specific CLA blend (80:20 cis-9,trans-11:trans-10,cis-12-CLA) induces regression of pre-established atherosclerosis in vivo, via modulation of monocyte/macrophage function. However, the exact mechanisms through which CLA mediates this effect remain to be elucidated. METHODS: Here, we address if CLA primes monocytes towards an anti-inflammatory MΦ2 macrophage and examine the effect of individual CLA isomers and the atheroprotective blend on monocyte-macrophage differentiation, cytokine generation, foam cell formation and cholesterol metabolism in human peripheral blood monocyte (HPBMC)-derived macrophages. RESULTS: cis-9,trans-11-CLA and the atheroprotective 80:20 CLA blend regulates expression of pro-inflammatory mediators and modulates the inflammatory cytokine profile of macrophages and foam cells. In addition, cis-9,trans-11-CLA and CLA blend primes HPBMCs towards an anti-inflammatory MΦ2 phenotype, characterised by increased scavenger receptor (CD36) and efflux protein (ABCA-1) expression. Furthermore, this altered macrophage phenotype impacts on foam cell formation, inhibiting ox-LDL accumulation and promoting cholesterol efflux via both PPARγ and LXRα dependent pathways. CONCLUSION: The data increases the understanding of the pathways regulated by CLA in atheroprotection, namely, inhibiting the progressive acquisition of a pro-inflammatory macrophage phenotype. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12950-015-0060-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-02-19 /pmc/articles/PMC4340802/ /pubmed/25722654 http://dx.doi.org/10.1186/s12950-015-0060-9 Text en © de Gaetano et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research de Gaetano, Monica Alghamdi, Kawthar Marcone, Simone Belton, Orina Conjugated linoleic acid induces an atheroprotective macrophage MΦ2 phenotype and limits foam cell formation |
title | Conjugated linoleic acid induces an atheroprotective macrophage MΦ2 phenotype and limits foam cell formation |
title_full | Conjugated linoleic acid induces an atheroprotective macrophage MΦ2 phenotype and limits foam cell formation |
title_fullStr | Conjugated linoleic acid induces an atheroprotective macrophage MΦ2 phenotype and limits foam cell formation |
title_full_unstemmed | Conjugated linoleic acid induces an atheroprotective macrophage MΦ2 phenotype and limits foam cell formation |
title_short | Conjugated linoleic acid induces an atheroprotective macrophage MΦ2 phenotype and limits foam cell formation |
title_sort | conjugated linoleic acid induces an atheroprotective macrophage mφ2 phenotype and limits foam cell formation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4340802/ https://www.ncbi.nlm.nih.gov/pubmed/25722654 http://dx.doi.org/10.1186/s12950-015-0060-9 |
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