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Conversion of M1 Macrophages to Foam Cells: Transcriptome Differences Determined by Sex
Background: M1 macrophages involved in pro-inflammatory processes can be induced by low-density lipoproteins (LDL), giving rise to foam cells. In the atheroma plaque, it has been identified that males present more advanced lesions associated with infiltration. Therefore, our study aims to investigat...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953229/ https://www.ncbi.nlm.nih.gov/pubmed/36831031 http://dx.doi.org/10.3390/biomedicines11020490 |
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author | Nambo-Venegas, Rafael Palacios-González, Berenice Mas-Oliva, Jaime Aurioles-Amozurrutia, Ana Karen Cruz-Rangel, Armando Moreno, Abel Hidalgo-Miranda, Alfredo Rodríguez-Dorantes, Mauricio Vadillo-Ortega, Felipe Xicohtencatl-Cortes, Juan Ruiz-Olmedo, María Isabel Reyes-Grajeda, Juan Pablo |
author_facet | Nambo-Venegas, Rafael Palacios-González, Berenice Mas-Oliva, Jaime Aurioles-Amozurrutia, Ana Karen Cruz-Rangel, Armando Moreno, Abel Hidalgo-Miranda, Alfredo Rodríguez-Dorantes, Mauricio Vadillo-Ortega, Felipe Xicohtencatl-Cortes, Juan Ruiz-Olmedo, María Isabel Reyes-Grajeda, Juan Pablo |
author_sort | Nambo-Venegas, Rafael |
collection | PubMed |
description | Background: M1 macrophages involved in pro-inflammatory processes can be induced by low-density lipoproteins (LDL), giving rise to foam cells. In the atheroma plaque, it has been identified that males present more advanced lesions associated with infiltration. Therefore, our study aims to investigate sex-related changes in the transcriptome of M1 macrophages during the internalization process of LDL particles. Methods: Peripheral blood mononuclear cells (PBMCs) from healthy male and female subjects were separated using Hystopaque, and monocytes were isolated from PBMCs using a positive selection of CD14+ cells. Cells were stimulated with LDL 10 µg/mL, and the transcriptional profile of M1 macrophages performed during LDL internalization was determined using a Clariom D platform array. Results: Chromosome Y influences the immune system and inflammatory responses in males expressing 43% of transcripts in response to LDL treatment. Males and females share 15 transcripts, where most correspond to non-coding elements involved in oxidative stress and endothelial damage. Conclusions: During LDL internalization, male monocyte-derived M1 macrophages display more marked proinflammatory gene expression. In contrast, female M1 macrophages display a more significant number of markers associated with cell damage. |
format | Online Article Text |
id | pubmed-9953229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99532292023-02-25 Conversion of M1 Macrophages to Foam Cells: Transcriptome Differences Determined by Sex Nambo-Venegas, Rafael Palacios-González, Berenice Mas-Oliva, Jaime Aurioles-Amozurrutia, Ana Karen Cruz-Rangel, Armando Moreno, Abel Hidalgo-Miranda, Alfredo Rodríguez-Dorantes, Mauricio Vadillo-Ortega, Felipe Xicohtencatl-Cortes, Juan Ruiz-Olmedo, María Isabel Reyes-Grajeda, Juan Pablo Biomedicines Article Background: M1 macrophages involved in pro-inflammatory processes can be induced by low-density lipoproteins (LDL), giving rise to foam cells. In the atheroma plaque, it has been identified that males present more advanced lesions associated with infiltration. Therefore, our study aims to investigate sex-related changes in the transcriptome of M1 macrophages during the internalization process of LDL particles. Methods: Peripheral blood mononuclear cells (PBMCs) from healthy male and female subjects were separated using Hystopaque, and monocytes were isolated from PBMCs using a positive selection of CD14+ cells. Cells were stimulated with LDL 10 µg/mL, and the transcriptional profile of M1 macrophages performed during LDL internalization was determined using a Clariom D platform array. Results: Chromosome Y influences the immune system and inflammatory responses in males expressing 43% of transcripts in response to LDL treatment. Males and females share 15 transcripts, where most correspond to non-coding elements involved in oxidative stress and endothelial damage. Conclusions: During LDL internalization, male monocyte-derived M1 macrophages display more marked proinflammatory gene expression. In contrast, female M1 macrophages display a more significant number of markers associated with cell damage. MDPI 2023-02-08 /pmc/articles/PMC9953229/ /pubmed/36831031 http://dx.doi.org/10.3390/biomedicines11020490 Text en © 2023 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 Nambo-Venegas, Rafael Palacios-González, Berenice Mas-Oliva, Jaime Aurioles-Amozurrutia, Ana Karen Cruz-Rangel, Armando Moreno, Abel Hidalgo-Miranda, Alfredo Rodríguez-Dorantes, Mauricio Vadillo-Ortega, Felipe Xicohtencatl-Cortes, Juan Ruiz-Olmedo, María Isabel Reyes-Grajeda, Juan Pablo Conversion of M1 Macrophages to Foam Cells: Transcriptome Differences Determined by Sex |
title | Conversion of M1 Macrophages to Foam Cells: Transcriptome Differences Determined by Sex |
title_full | Conversion of M1 Macrophages to Foam Cells: Transcriptome Differences Determined by Sex |
title_fullStr | Conversion of M1 Macrophages to Foam Cells: Transcriptome Differences Determined by Sex |
title_full_unstemmed | Conversion of M1 Macrophages to Foam Cells: Transcriptome Differences Determined by Sex |
title_short | Conversion of M1 Macrophages to Foam Cells: Transcriptome Differences Determined by Sex |
title_sort | conversion of m1 macrophages to foam cells: transcriptome differences determined by sex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953229/ https://www.ncbi.nlm.nih.gov/pubmed/36831031 http://dx.doi.org/10.3390/biomedicines11020490 |
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