Conversion of M1 Macrophages to Foam Cells: Transcriptome Differences Determined by Sex

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-relate...

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Published inBiomedicines Vol. 11; no. 2; p. 490
Main Authors 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
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 01.02.2023
MDPI
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Summary: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. 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. 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. 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.
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ISSN:2227-9059
2227-9059
DOI:10.3390/biomedicines11020490