Related Experiment Videos
Evidence that glutamine is involved in neutrophil function
Tania C Pithon-Curi1, Ariane G Trezena, Wothan Tavares-Lima
1Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, SP, Brazil. tcuri@fisio.icb.usp.br
Cell Biochemistry and Function
|April 30, 2002
Summary
Phosphate-dependent glutaminase (PDG) activity in neutrophils differs based on location and stimulus. Glutamine may preserve neutrophil function during infections and injuries.
Area of Science:
- Immunology
- Cellular Metabolism
Background:
- Neutrophils play a critical role in immune responses.
- Glutamine metabolism, regulated by phosphate-dependent glutaminase (PDG), is crucial for immune cell function.
Purpose of the Study:
- To investigate how PDG activity in neutrophils varies between the peritoneal cavity (PC) and bronchoalveolar space (BAS).
- To examine the impact of different stimuli (saline, glycogen, LPS) on PDG activity in neutrophils from these sites.
- To assess the effect of glutamine on nitric oxide (NO) and tumor necrosis factor (TNF) production by neutrophils.
Main Methods:
- Neutrophils were isolated from PC and BAS of rats after administration of saline, glycogen, or lipopolysaccharide (LPS).
- PDG activity was measured in these neutrophils.
- Peritoneal neutrophils were cultured with LPS and varying concentrations of glutamine to assess NO and TNF production.
Main Results:
- PDG activity in neutrophils was significantly modulated by both the site of origin (PC vs. BAS) and the administered stimulus.
- Cells from BAS showed increased PDG activity with glycogen and LPS compared to saline.
- Cells from PC exhibited distinct PDG activity patterns, with LPS significantly increasing activity.
- Glutamine supplementation did not significantly affect NO production but decreased TNF production in LPS-stimulated peritoneal neutrophils.
Conclusions:
- Neutrophil PDG activity is site-dependent and stimulus-responsive.
- Glutamine may play a protective role in neutrophil function during inflammatory conditions by modulating cytokine production.