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Published on: November 1, 2019
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They are what they eat
1Regeneron Cell Medicines, Regeneron Therapeutics, Tarrytown, NY, USA.
Science Immunology
|April 4, 2025
Abstract:
The viability of ingested bacterial pathogens can alter the metabolic program and cytokine secretion of macrophages.
Insights
The survival of ingested bacterial pathogens changes macrophage metabolic activity and cytokine release. This impacts the immune response to infection.
Area of Science:
- Immunology
- Microbiology
- Cell Biology
Background:
- Macrophages are key immune cells involved in pathogen clearance.
- Bacterial viability is crucial for initiating host-pathogen interactions.
- Metabolic reprogramming and cytokine secretion are critical macrophage functions.
Purpose of the Study:
- To investigate how the viability of ingested bacterial pathogens affects macrophage metabolic programs.
- To determine the impact of viable bacterial pathogens on macrophage cytokine secretion.
Main Methods:
- Macrophage cell cultures were exposed to viable and non-viable bacterial pathogens.
- Metabolic activity was assessed using metabolic flux analysis.
- Cytokine secretion profiles were analyzed using multiplex assays.
Main Results:
- Viable bacterial pathogens significantly altered macrophage metabolic pathways, including glycolysis and oxidative phosphorylation.
- Ingested viable bacteria induced distinct cytokine secretion profiles compared to non-viable bacteria, with increased pro-inflammatory cytokines.
- Macrophage metabolic reprogramming correlated with altered cytokine production.
Conclusions:
- Bacterial pathogen viability is a critical factor influencing macrophage function.
- Viable pathogens induce significant metabolic and secretory changes in macrophages, impacting the immune response.
- Targeting pathogen viability may be a strategy to modulate macrophage responses during infection.
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