They are what they eat

Asha Pillai1

  • 1Regeneron Cell Medicines, Regeneron Therapeutics, Tarrytown, NY, USA.

Science Immunology
|April 4, 2025
PubMed

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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