The Critical Role of Cell Metabolism for Essential Neutrophil Functions
Curi, R; Levada-Pires, AC; Silva, EBD; Poma, SO; Zambonatto, RF; Domenech, P; Almeida, MM; Gritte, RB; Souza-Siqueira, T; Gorjão, R; Newsholme, P; Pithon-Curi, TC
| HERO ID | 7456045 |
|---|---|
| Material Type | Review |
| In Press | No |
| Year | 2020 |
| Title | The Critical Role of Cell Metabolism for Essential Neutrophil Functions |
| Authors | Curi, R; Levada-Pires, AC; Silva, EBD; Poma, SO; Zambonatto, RF; Domenech, P; Almeida, MM; Gritte, RB; Souza-Siqueira, T; Gorjão, R; Newsholme, P; Pithon-Curi, TC |
| Journal | Cellular Physiology and Biochemistry |
| Volume | 54 |
| Issue | 4 |
| Page Numbers | 629-647 |
| Abstract | Neutrophils were traditionally considered as short-lived cells with abundant secretory and protein synthetic activity. Recent studies, however, indicate neutrophils are in reality a heterogeneous population of cells. Neutrophils differentiate from pluripotent stem cells in the bone marrow, and can further mature in the blood stream and can have different phenotypes in health and disease conditions. Neutrophils undergo primary functions such as phagocytosis, production of reactive oxygen species (ROS), release of lipid mediators and inflammatory proteins (mainly cytokines), and apoptosis. Neutrophils stimulate other neutrophils and trigger a cascade of immune and inflammatory responses. The underpinning intracellular metabolisms that support these neutrophil functions are herein reported. It has been known for many decades that neutrophils utilize glucose as a primary fuel and produce lactate as an end product of glycolysis. Neutrophils metabolize glucose through glycolysis and the pentose- phosphate pathway (PPP). Mitochondrial glucose oxidation is very low. The PPP provides the reduced nicotinamide adenine dinucleotide phosphate (NADPH) for the NADPH-oxidase (NOX) complex activity to produce superoxide from oxygen. These cells also utilize glutamine and fatty acids to produce the required adenosine triphosphate (ATP) and precursors for the synthesis of molecules that trigger functional outcomes. Neutrophils obtained from rat intraperitoneal cavity and incubate for 1 hour at 37°C metabolize glutamine at higher rate than that of glucose. Glutamine delays neutrophil apoptosis and maintains optimal NOX activity for superoxide production. Under limited glucose provision, neutrophils move to fatty acid oxidation (FAO) to obtain the required energy for the cell function. FAO is mainly associated with neutrophil differentiation and maturation. Hypoxia, hormonal dysfunction, and physical exercise markedly change neutrophil metabolism. It is now become clear that neutrophil metabolism underlies the heterogeneity of neutrophil phenotypes and should be intense focus of investigation. |
| Doi | 10.33594/000000245 |
| Pmid | 32589830 |
| Is Certified Translation | No |
| Dupe Override | No |
| Comments | Scopus URL: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85087321063&doi=10.33594%2f000000245&partnerID=40&md5=6afc747cc8e86e4561706c287125c01d |
| Is Public | Yes |
| Language Text | English |
| Keyword | Glucose; Glutamine; Hormones; Inflammation; Physical exercise |