M-CSF- and L929-derived macrophages present distinct metabolic profiles with similar inflammatory outcomes
Autor: | Jessica Aparecida da Silva Pereira, Cristhiane Favero de Aguiar, Pedro M. Moraes-Vieira, Felipe Corrêa da Silva, Leonardo Pimentel de Freitas, Jessica Rodrigues de Andrade, Lauar de Brito Monteiro, Ana Campos Codo, Gustavo Gastão Davanzo |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Immunology Mitochondrion Proinflammatory cytokine Cell Line 03 medical and health sciences Mice 0302 clinical medicine Immune system medicine Immunology and Allergy Macrophage Animals Metabolomics Secretion Chemistry Macrophage Colony-Stimulating Factor Macrophages Hematology In vitro Cell biology 030104 developmental biology medicine.anatomical_structure Interleukin 12 Metabolome Cytokines Bone marrow Inflammation Mediators Energy Metabolism Biomarkers 030215 immunology |
Zdroj: | Immunobiology. 225(3) |
ISSN: | 1878-3279 |
Popis: | Macrophages are essential components of the immune system. Macrophages can be derived from the bone marrow of mice with either recombinant M-CSF or L929 supernatant. Recent literature considers recombinant M-CSF- and L929-derived macrophages as equals, even though L929-derived macrophages are exposed to other substances secreted in the L929 supernatant, and not only M-CSF. Thus, we decided to perform a comparative analysis of both inflammatory and metabolic profiles of macrophages differentiated under the aforementioned conditions, which is relevant for standardization and interpretation of in vitro studies. We observed that, when treated with LPS, L929macs secrete lower levels of proinflammatory cytokines (TNF-α, IL-6, IL12) and present higher glycolysis and oxygen consumption when compared with M-CSFmacs. L929macs also have increased mitochondrial mass, with higher percentage of dysfunctional mitochondria. This sort of information can help direct further studies towards a more specific approach for macrophage generation. |
Databáze: | OpenAIRE |
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