Frontiers in Pharmacology (Oct 2024)

Capsaicin attenuates the effect of inflammatory cytokines in a HaCaT cell model for basal keratinocytes

  • Maria Fernanda Cervantes Recalde,
  • Maria Fernanda Cervantes Recalde,
  • Jana Schmidt,
  • Cristina Girardi,
  • Marco Massironi,
  • Markus Leo Rechl,
  • Markus Leo Rechl,
  • Markus Leo Rechl,
  • Joachim Hans,
  • Dominik Stuhlmann,
  • Veronika Somoza,
  • Veronika Somoza,
  • Barbara Lieder,
  • Barbara Lieder,
  • Barbara Lieder

DOI
https://doi.org/10.3389/fphar.2024.1474898
Journal volume & issue
Vol. 15

Abstract

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IntroductionThe resolution of the skin’s inflammatory response is only possible if its barrier function is restored. TRPV1 channel activation plays an important role during inflammation but the effect of this activation on the skin barrier under inflammatory conditions has not been clarified. We hypothesize that it could potentially aid the keratinocyte barrier by reducing inflammatory cytokine release and promoting tight junction development.MethodsTo explore the role of TRPV1 activation in inflammation, we designed and optimized an in vitro model of keratinocytes with basal epidermal layer characteristics using HaCaT cells and TNFα to induce inflammation.ResultsTNFα increased the gene expression of tight junction protein claudin 1 (CLDN1) by at least 2.60 ± 0.16-fold, in a concentration-dependent manner, over a 48 h period. The administration of a capsaicin pre-treatment reduced the CLDN1 expression to 1.51 ± 0.16-fold during the first 6 h after TNFα induction, whereas IL-8 cytokine release was reduced 0.64 ± 0.17-fold. After 48 h, CLDN1 protein levels increased by a factor of 6.57 ± 1.39 compared to cells only treated with TNFα.DiscussionThese results suggest that activation of TRPV1 by capsaicin can potentiate the increase in CLDN1 expression and CLDN1 protein synthesis induced by TNFα in cultured keratinocytes, while reducing the release of IL-8.

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