House dust mite extract activates apical Cl(-) channels through protease-activated receptor 2 in human airway

Hyung-Ju Cho1, Jae Young Choi, Yu-Mi Yang

  • 1Department of Otorhinolaryngology, Hallym University College of Medicine, Seoul, South Korea.

Insights

House dust mite extract activates protease-activated receptor-2 (PAR-2), increasing airway fluid secretion via chloride channels. This finding is crucial for understanding allergic rhinitis and mucociliary clearance.

Area of Science:

  • Respiratory Medicine
  • Cell Biology
  • Immunology

Background:

  • Airway mucosal fluid secretion is vital for mucociliary clearance.
  • Fluid hypersecretion characterizes inflammatory airway diseases like allergic rhinitis.
  • House dust mite (HDM) extract activates protease-activated receptors (PARs) in airway epithelia, but its role in ion transport and fluid secretion is unknown.

Purpose of the Study:

  • To investigate the effect of HDM extract on ion transport and fluid secretion in human nasal epithelial cells.
  • To elucidate the role of protease-activated receptor-2 (PAR-2) in HDM-induced airway responses.

Main Methods:

  • Primary human nasal epithelial cells were used to measure intracellular calcium concentration ([Ca(2+)](i)) using Fura2-AM spectrofluorometry.
  • Short-circuit current (Isc) was measured using Ussing chambers.
  • Fluid secretion was assessed in porcine airway mucosa via optical measurement.

Main Results:

  • HDM extract activated PAR-2, leading to a significant increase in [Ca(2+)](i).
  • HDM induced Isc that was sensitive to inhibitors of cystic fibrosis transmembrane conductance regulator (CFTR) and calcium-activated chloride channels (CaCC).
  • HDM extract stimulated fluid secretion in porcine airway mucosa.

Conclusions:

  • HDM extract activates PAR-2, stimulating apical chloride secretion through CaCC and CFTR channels.
  • HDM-induced fluid secretion in airway mucosa suggests a role for PAR-2 in mucociliary clearance and hypersecretory responses to airborne allergens.

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