Co-Stimulation with TWEAK and TGF-β1 Induces Steroid-Insensitive TSLP and CCL5 Production in BEAS-2B Human Bronchial Epithelial Cells

Int J Mol Sci. 2024 Oct 29;25(21):11625. doi: 10.3390/ijms252111625.

Abstract

Steroid-resistant asthma is a common cause of refractory asthma. Type 2 inflammation is the main inflammatory response in asthma, and the mechanism underlying the steroid-resistance of type 2 inflammation has not been completely elucidated. Tumor-necrosis-factor-like apoptosis-inducing factor (TWEAK) and transforming growth factor (TGF)-β1 are involved in epithelial-mesenchymal transition (EMT) and the production of thymic stromal lymphopoietin (TSLP) and C-C motif chemokine ligand 5 (CCL5). We herein hypothesize that the combined exposure to TWEAK and TGF-β1 may result in the development of steroid resistance in bronchial epithelial cells. The bronchial epithelial cell line BEAS-2B was cultured with or without TGF-β1 or TWEAK, in the presence or absence of dexamethasone (DEX). The roles of Smad-independent pathways and MAP kinase phosphatase 1 (MKP-1) were also explored. Co-stimulation of TWEAK and TGF-β1 induced E-cadherin reduction, N-cadherin upregulation, and TSLP and CCL5 production, which were not suppressed by DEX. Inhibition of the nuclear factor kappa beta (NF-κB) and mitogen-activated protein kinase pathways downregulated steroid-unresponsive TSLP and CCL5 production, whereas knockdown of MKP-1 improved steroid-unresponsive TSLP production, induced by co-stimulation with TWEAK and TGF-β1. Therefore, co-stimulation with TWEAK and TGF-β1 can induce the steroid-insensitive production of TSLP and CCL5 in the bronchial epithelium and may contribute to airway inflammation.

Keywords: CCL5; EMT; MKP-1; TGF-β1; TSLP; TWEAK; asthma.

MeSH terms

  • Bronchi* / cytology
  • Bronchi* / drug effects
  • Bronchi* / metabolism
  • Cadherins / metabolism
  • Cell Line
  • Chemokine CCL5* / metabolism
  • Cytokine TWEAK* / metabolism
  • Cytokines* / metabolism
  • Dexamethasone* / pharmacology
  • Dual Specificity Phosphatase 1 / genetics
  • Dual Specificity Phosphatase 1 / metabolism
  • Epithelial Cells* / drug effects
  • Epithelial Cells* / metabolism
  • Epithelial-Mesenchymal Transition / drug effects
  • Humans
  • NF-kappa B / metabolism
  • Signal Transduction / drug effects
  • Thymic Stromal Lymphopoietin*
  • Transforming Growth Factor beta1* / metabolism

Substances

  • Cytokine TWEAK
  • Chemokine CCL5
  • Transforming Growth Factor beta1
  • Cytokines
  • Thymic Stromal Lymphopoietin
  • Dexamethasone
  • TSLP protein, human
  • TNFSF12 protein, human
  • CCL5 protein, human
  • NF-kappa B
  • Dual Specificity Phosphatase 1
  • DUSP1 protein, human
  • Cadherins
  • TGFB1 protein, human

Grants and funding

This research was funded in part by JSPS KAKENHI, grant number 23K07658.