Staphylococcus aureus Serine protease-like protein A (SplA) induces IL-8 by keratinocytes and synergizes with IL-17A

Cytokine. 2024 Aug:180:156634. doi: 10.1016/j.cyto.2024.156634. Epub 2024 May 28.

Abstract

Background: Serine protease-like (Spl) proteins produced by Staphylococcus (S.) aureus have been associated with allergic inflammation. However, effects of Spls on the epidermal immune response have not been investigated.

Objectives: To assess the epidermal immune response to SplA, SplD and SplE dependent on differentiation of keratinocytes and a Th2 or Th17 cytokine milieu.

Methods: Human keratinocytes of healthy controls and a STAT3-hyper-IgE syndrome (STAT3-HIES) patient were cultured in different calcium concentrations in the presence of Spls and Th2 or Th17 cytokines. Keratinocyte-specific IL-8 production and concomitant migration of neutrophils were assessed.

Results: SplE and more significantly SplA, induced IL-8 in keratinocytes. Suprabasal-like keratinocytes showed a higher Spl-mediated IL-8 production and neutrophil migration compared to basal-like keratinocytes. Th17 cytokines amplified Spl-mediated IL-8 production, which correlated with neutrophil recruitment. Neutrophil recruitment by keratinocytes of the STAT3-HIES patient was similar to healthy control cells.

Conclusion: S. aureus-specific Spl proteases synergized with IL-17A on human keratinocytes with respect to IL-8 release and neutrophil migration, highlighting the importance of keratinocytes and Th17 immunity in barrier function.

Keywords: Keratinocytes; Neutrophil migration; S. aureus; STAT3-hyper IgE syndrome (HIES); Serine protease-like proteins (Spls); Th2/Th17 immunity.

MeSH terms

  • Bacterial Proteins / metabolism
  • Cell Movement / drug effects
  • Cells, Cultured
  • Humans
  • Interleukin-17* / metabolism
  • Interleukin-8* / metabolism
  • Keratinocytes* / drug effects
  • Keratinocytes* / immunology
  • Keratinocytes* / metabolism
  • Neutrophils* / immunology
  • Neutrophils* / metabolism
  • STAT3 Transcription Factor / metabolism
  • Serine Proteases / metabolism
  • Staphylococcus aureus* / immunology
  • Th17 Cells / immunology
  • Th17 Cells / metabolism

Substances

  • Interleukin-17
  • Interleukin-8
  • IL17A protein, human
  • Bacterial Proteins
  • STAT3 Transcription Factor
  • CXCL8 protein, human
  • Serine Proteases