Anti-inflammatory effects of yeast-derived vacuoles on LPS-induced murine macrophage activation

Su-Min Lee1, Yang-Hoon Kim2, Jiho Min1

  • 1Graduate School of Semiconductor and Chemical Engineering, Jeonbuk National University , Jeonbuk, South Korea.

Microbiology Spectrum
|September 25, 2023
PubMed
Abstract

Insights

Vacuoles from Saccharomyces cerevisiae yeast show significant anti-inflammatory effects by reducing key inflammatory mediators and inhibiting the NF-κB pathway in macrophages, suggesting potential therapeutic applications for inflammatory diseases.

Area of Science:

  • Immunology
  • Microbiology
  • Biochemistry

Background:

  • Vacuoles from Saccharomyces cerevisiae share functional similarities with mammalian lysosomes.
  • Dysregulated inflammation is implicated in various chronic diseases.
  • Lipopolysaccharide (LPS) is a potent inducer of inflammatory responses in macrophages.

Purpose of the Study:

  • To evaluate the anti-inflammatory efficacy of Saccharomyces cerevisiae-derived vacuoles.
  • To investigate the modulation of inflammatory mediators and signaling pathways by these vacuoles.

Main Methods:

  • Treatment of macrophages with varying concentrations of S. cerevisiae-derived vacuoles.
  • Assessment of inflammatory mediator expression (iNOS, TNF-α, IL-1β, IL-6) via protein and mRNA analysis.
  • Immunofluorescence analysis to track nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) translocation.

Main Results:

  • S. cerevisiae-derived vacuoles significantly inhibited LPS-induced expression of iNOS protein and mRNA.
  • Vacuoles markedly reduced mRNA levels of TNF-α, IL-1β, and IL-6 in LPS-stimulated macrophages.
  • Vacuoles suppressed NF-κB pathway activation in LPS-stimulated macrophages.

Conclusions:

  • S. cerevisiae-derived vacuoles demonstrate potent anti-inflammatory properties by downregulating the NF-κB pathway.
  • These findings highlight the potential of S. cerevisiae-derived vacuoles as a novel therapeutic agent for inflammatory conditions.
  • Further in vivo studies are warranted to confirm efficacy and safety.

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