Airway Exposure to Polyethyleneimine Nanoparticles Induces Type 2 Immunity by a Mechanism Involving Oxidative Stress and ATP Release

Int J Mol Sci. 2021 Aug 23;22(16):9071. doi: 10.3390/ijms22169071.

Abstract

Polyethyleneimine (PEI) induced immune responses were investigated in human bronchial epithelial (hBE) cells and mice. PEI rapidly induced ATP release from hBE cells and pretreatment with glutathione (GSH) blocked the response. PEI activated two conductive pathways, VDAC-1 and pannexin 1, which completely accounted for ATP efflux across the plasma membrane. Moreover, PEI increased intracellular Ca2+ concentration ([Ca2+]i), which was reduced by the pannexin 1 inhibitor, 10Panx (50 μM), the VDAC-1 inhibitor, DIDS (100 μM), and was nearly abolished by pretreatment with GSH (5 mM). The increase in [Ca2+]i involved Ca2+ uptake through two pathways, one blocked by oxidized ATP (oATP, 300 μM) and another that was blocked by the TRPV-1 antagonist A784168 (100 nM). PEI stimulation also increased IL-33 mRNA expression and protein secretion. In vivo experiments showed that acute (4.5 h) PEI exposure stimulated secretion of Th2 cytokines (IL-5 and IL-13) into bronchoalveolar lavage (BAL) fluid. Conjugation of PEI with ovalbumin also induced eosinophil recruitment and secretion of IL-5 and IL-13 into BAL fluid, which was inhibited in IL-33 receptor (ST2) deficient mice. In conclusion, PEI-induced oxidative stress stimulated type 2 immune responses by activating ATP-dependent Ca2+ uptake leading to IL-33 secretion, similar to allergens derived from Alternaria.

Keywords: IL-33; Th2 cytokines; allergic inflammation; intracellular Ca2+; purinergic signaling.

MeSH terms

  • Adenosine Triphosphate / immunology*
  • Allergens / immunology
  • Animals
  • Calcium / immunology
  • Cells, Cultured
  • Cytokines / immunology
  • Epithelial Cells / drug effects*
  • Epithelial Cells / immunology*
  • Female
  • Humans
  • Immunity / drug effects*
  • Immunity / immunology
  • Mice
  • Mice, Inbred BALB C
  • Nanoparticles / administration & dosage*
  • Oxidative Stress / drug effects*
  • Oxidative Stress / immunology
  • Polyethyleneimine / pharmacology*
  • RNA, Messenger / immunology
  • Respiratory Mucosa / drug effects
  • Respiratory Mucosa / immunology

Substances

  • Allergens
  • Cytokines
  • RNA, Messenger
  • Adenosine Triphosphate
  • Polyethyleneimine
  • Calcium