Increased internalization of Staphylococcus aureus and cytokine expression in human Wharton's jelly mesenchymal stem

Jérôme Josse1, Frédéric Velard2, Saad Mechiche Alami3

  • 1EA 4691 «Biomatériaux et Inflammation en Site Osseux», Pôle Santé, SFR CAP-Santé (FED 4231), Université de Reims Champagne-Ardenne, Reims, France UFR de Pharmacie, URCA, Reims, France.

Abstract

Insights

Human Wharton's jelly-mesenchymal stem cells (WJ-MSCs) internalize Staphylococcus aureus (S. aureus), increasing IL-6 and TNF-α production. This suggests WJ-MSCs play a role in the immune response to bacterial infections.

Area of Science:

  • Immunology
  • Stem Cell Biology
  • Microbiology

Background:

  • Mesenchymal stem cells (MSCs) interact with immune cells, but bacterial interactions with MSCs are less understood.
  • This study explores the impact of Staphylococcus aureus (S. aureus) on human Wharton's jelly-MSCs (WJ-MSCs).

Purpose of the Study:

  • To determine if WJ-MSCs internalize S. aureus.
  • To assess WJ-MSC survival after S. aureus exposure.
  • To investigate the release of immunomodulatory mediators by WJ-MSCs following S. aureus interaction.

Main Methods:

  • WJ-MSCs were exposed to S. aureus at multiplicities of infection (MOI) of 10:1 and 30:1.
  • Intracellular S. aureus and WJ-MSC viability were quantified.
  • Cytokine expression (IL-6 mRNA) and secretion (TNF-α) were measured using qRT-PCR and ELISA.

Main Results:

  • WJ-MSCs internalized S. aureus in a time-dependent manner up to six hours post-infection.
  • Increased expression of IL-6 mRNA and secretion of TNF-α were observed at six and nine hours post-infection.
  • No significant impact on WJ-MSC viability was explicitly stated in the results.

Conclusions:

  • WJ-MSCs demonstrate the capacity to internalize S. aureus.
  • These findings highlight a potential role for WJ-MSCs in the immune response against bacterial pathogens.

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