Rhinoviral stimuli, epithelial factors and ATP signalling contribute to bronchial smooth muscle production of IL-33

J Transl Med. 2015 Aug 29:13:281. doi: 10.1186/s12967-015-0645-3.

Abstract

Background: Bronchial smooth muscle cells (BSMCs) from severe asthmatics have been shown to overexpress the Th2-driving and asthma-associated cytokine IL-33. However, little is known regarding factors involved in BSMC production of IL-33. Rhinovirus (RV) infections cause asthma exacerbations, which exhibit features of Th2-type inflammation. Here, we investigated the effects of epithelial-derived media and viral stimuli on IL-33 expression in human BSMCs.

Methods: Primary human BSMCs from healthy (n = 3) and asthmatic (n = 3) subjects were stimulated with conditioned media from primary human bronchial epithelial cells (BECs), double-stranded (ds)RNA, dsRNA/LyoVec, or infected with RV. BSMCs were also pretreated with the purinergic receptor antagonist suramin. IL-33 expression was analysed by RT-qPCR and western blot and ATP levels were determined in cell supernatants.

Results: RV infection and activation of TLR3 by dsRNA increased IL-33 mRNA and protein in healthy and asthmatic BSMCs. These effects were inhibited by dexamethasone. BSMC expression of IL-33 was also increased by stimulation of RIG-I-like receptors using dsRNA/LyoVec. Conditioned media from BECs induced BSMC expression of IL-33, which was further enhanced by dsRNA. BEC-derived medium and viral-stimulated BSMC supernatants exhibited elevated ATP levels. Blocking of purinergic signalling with suramin inhibited BSMC expression of IL-33 induced by dsRNA and BEC-derived medium.

Conclusions: RV infection of BSMCs and activation of TLR3 and RIG-I-like receptors cause expression and production of IL-33. Epithelial-released factor(s) increase BSMC expression of IL-33 and exhibit positive interaction with dsRNA. Increased BSMC IL-33 associates with ATP release and is antagonised by suramin. We suggest that epithelial-derived factors contribute to baseline BSMC IL-33 production, which is further augmented by RV infection of BSMCs and stimulation of their pathogen-recognising receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Asthma / metabolism*
  • Asthma / virology
  • Bronchi / cytology
  • Bronchi / virology
  • Cells, Cultured
  • Culture Media, Conditioned / chemistry
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases / metabolism
  • Dexamethasone / chemistry
  • Epithelium / virology*
  • Humans
  • Inflammation / metabolism
  • Interleukin-33 / metabolism*
  • Myocytes, Smooth Muscle / metabolism*
  • Myocytes, Smooth Muscle / virology
  • Picornaviridae Infections / metabolism
  • Picornaviridae Infections / virology
  • RNA, Double-Stranded / metabolism
  • Receptors, Immunologic
  • Rhinovirus*
  • Signal Transduction
  • Suramin / chemistry
  • Th2 Cells / cytology
  • Toll-Like Receptor 3 / metabolism

Substances

  • Culture Media, Conditioned
  • IL33 protein, human
  • Interleukin-33
  • RNA, Double-Stranded
  • Receptors, Immunologic
  • TLR3 protein, human
  • Toll-Like Receptor 3
  • Suramin
  • Dexamethasone
  • Adenosine Triphosphate
  • RIGI protein, human
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases