| Autor: |
Vigeland CL; University of North Carolina at Chapel Hill School of Medicine, Medicine, Chapel Hill, North Carolina, United States; christine_vigeland@med.unc.edu., Link JD; The University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, United States., Beggs HS; The University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, United States., Alwarawrah Y; The University of North Carolina at Chapel Hill School of Medicine, Pediatrics, Chapel Hill, North Carolina, United States., Ehrmann BM; The University of North Carolina at Chapel Hill, Chemistry, Chapel Hill, North Carolina, United States., Dang H; UNC, Marsico Lung Institute, Chapel Hill, North Carolina, United States., Doerschuk CM; Rainbow Babies & Children Hospital, Cleveland, Ohio, United States. |
| Abstrakt: |
Changes in metabolic activity are key regulators of macrophage activity. Pro-inflammatory macrophages upregulate glycolysis, which promotes an inflammatory phenotype, whereas pro-repair macrophages rely upon oxidative metabolism and glutaminolysis to support their activity. Work to understand how metabolism regulates macrophage phenotype has been done primarily in macrophage cell lines and bone marrow-derived macrophages (BMDM). Our study sought to understand changes in metabolic activity of murine tissue-resident alveolar macrophages (AM) in response to LPS stimulation and to contrast them to BMDM. These studies also determined the contribution of glutamine metabolism using the glutamine inhibitor, DON. We found that compared to BMDM, AM have higher rates of oxygen consumption and contain a higher concentration of intracellular metabolites involved in fatty acid oxidation. In response to LPS, BMDM but not AM increased rates of glycolysis. Inhibition of glutamine metabolism using DON altered the metabolic activity of AM but not BMDM. Within AM, glutamine inhibition led to increases in intracellular metabolites involved in glycolysis, the TCA cycle, fatty acid oxidation, and amino acid metabolism. Glutamine inhibition also altered the metabolic response to LPS within AM but not BMDM. Our data reveal striking differences in the metabolic activity of AM and BMDM. |
