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


Por: Nambo-Venegas, Rafael, Palacios-Gonzalez, Berenice, Mas-Oliva, Jaime, Aurioles-Amozurrutia, Ana Karen, Cruz-Rangel, Armando, Moreno, Abel, Hidalgo-Miranda, Alfredo, Rodriguez-Dorantes, Mauricio, Vadillo-Ortega, Felipe, Xicohtencatl-Cortes, Juan, Ruiz-Olmedo, Maria Isabel, Reyes-Grajeda, Juan Pablo

Publicada: 1 feb 2023
Resumen:
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 mu g/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.

Filiaciones:
Nambo-Venegas, Rafael:
 Laboratorio de Estructura de Proteínas, Instituto Nacional de Medicina Genómica, Mexico City, 14600, Mexico

Palacios-Gonzalez, Berenice:
 Laboratorio de Envejecimiento Saludable, Centro de Investigación Sobre Envejecimiento (CIE-CINVESTAV Sur), Instituto Nacional de Medicina Genómica, Mexico City, 14330, Mexico

Mas-Oliva, Jaime:
 Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City, 04510, Mexico

Aurioles-Amozurrutia, Ana Karen:
 Laboratorio de Estructura de Proteínas, Instituto Nacional de Medicina Genómica, Mexico City, 14600, Mexico

Cruz-Rangel, Armando:
 Laboratorio de Estructura de Proteínas, Instituto Nacional de Medicina Genómica, Mexico City, 14600, Mexico

Moreno, Abel:
 Instituto de Química, Universidad Nacional Autónoma de México, Mexico City, 04510, Mexico

Hidalgo-Miranda, Alfredo:
 Laboratorio de Genómica del Cáncer, Instituto Nacional de Medicina Genómica, Mexico City, 14600, Mexico

Rodriguez-Dorantes, Mauricio:
 Laboratorio de Oncogenomica, Instituto Nacional de Medicina Genómica, Mexico City, 14600, Mexico

Vadillo-Ortega, Felipe:
 Unidad de Vinculación Científica de la Facultad de Medicina UNAM en INMEGEN, Instituto Nacional de Medicina Genómica, Mexico City, 14600, Mexico

Xicohtencatl-Cortes, Juan:
 Laboratorio de Bacteriología Intestinal, Hospital Infantil de México Federico Gómez, Mexico City, 06720, Mexico

Ruiz-Olmedo, Maria Isabel:
 ROPPEN RT de R.L. de C.V., Mexico City, 14650, Mexico

Reyes-Grajeda, Juan Pablo:
 Laboratorio de Estructura de Proteínas, Instituto Nacional de Medicina Genómica, Mexico City, 14600, Mexico
ISSN: 22279059





Biomedicines
Editorial
MDPI AG, ST ALBAN-ANLAGE 66, CH-4052 BASEL, SWITZERLAND, Suiza
Tipo de documento: Article
Volumen: 11 Número: 2
Páginas:
WOS Id: 000938960400001
ID de PubMed: 36831031
imagen gold, All Open Access; Gold

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