Candida albicans Modifies the Protein Composition and Size Distribution of THP-1 Macrophage-Derived Extracellular

Jose Antonio Reales-Calderón1,2, Catarina Vaz1,2, Lucía Monteoliva1,2

  • 1Departamento de Microbiología II, Facultad de Farmacia, Universidad Complutense de Madrid Plaza de Ramón y Cajal s/n , Madrid 28040, Spain.

Insights

Macrophages release extracellular vesicles (EVs) that communicate during Candida albicans infections. This study quantifies EV proteins, revealing changes that impact immune responses and pathogen clearance.

Area of Science:

  • Immunology
  • Cell Biology
  • Proteomics

Background:

  • Macrophages are critical for clearing systemic candidiasis.
  • Extracellular vesicles (EVs) mediate immune cell communication.
  • EV cargo changes can influence immune responses to infection.

Purpose of the Study:

  • To perform the first quantitative proteomic analysis of THP-1 macrophage-derived EVs during Candida albicans interaction.
  • To identify changes in EV protein composition and size.
  • To understand the role of macrophage EVs in antifungal immunity.

Main Methods:

  • Quantitative proteomic analysis of THP-1 macrophage-derived EVs.
  • EVs isolated from THP-1 macrophages interacting with Candida albicans.
  • Identification and quantification of 717 proteins in EVs.
  • Functional assays on recipient THP-1 cells.

Main Results:

  • Identified 717 proteins in THP-1 macrophage EVs, with 133 showing altered abundance upon Candida albicans interaction.
  • Differentially abundant proteins were linked to immune response, signaling, and cytoskeletal reorganization.
  • EVs from both control and infected macrophages activated recipient macrophages, enhancing cytokine secretion and candidacidal activity.

Conclusions:

  • Macrophage-derived EVs play a significant role in the response to Candida albicans infection.
  • EVs modulate immune cell communication and function during fungal infections.
  • This study provides novel insights into the proteomic landscape of EVs in antifungal immunity.