Enhancement of airway ciliary beating mediated via voltage-gated Ca2+ channels/α7-nicotinic receptors in mice

Pflugers Arch. 2022 Oct;474(10):1091-1106. doi: 10.1007/s00424-022-02724-5. Epub 2022 Jul 11.

Abstract

Acetylcholine (ACh), which activates muscarinic ACh receptors (mAChRs) and nicotinic ACh receptors (nAChRs), enhances airway ciliary beating by increasing the intracellular Ca2+ concentration ([Ca2+]i). The mechanisms enhancing airway ciliary beating by nAChRs have remained largely unknown, although those by mAChRs are well understood. In this study, we focused on the effects of α7-nAChRs and voltage-gated Ca2+ channels (CaVs) on the airway ciliary beating. The activities of ciliary beating were assessed by frequency (CBF, ciliary beat frequency) and amplitude (CBD, ciliary bend distance) measured by high-speed video microscopy. ACh enhanced CBF and CBD by 25% mediated by an [Ca2+]i increase stimulated by mAChRs and α7-nAChRs (a subunit of nAChR) in airway ciliary cells of mice. Experiments using PNU282987 (an agonist of α7-nAChR) and MLA (an inhibitor of α7-nAChR) revealed that CBF and CBD enhanced by α7-nAChR are approximately 50% of those enhanced by ACh. CBF, CBD, and [Ca2+]i enhanced by α7-nAChRs were inhibited by nifedipine, suggesting activation of CaVs by α7-nAChRs. Experiments using a high K+ solution with/without nifedipine (155.5 mM K+) showed that the activation of CaVs enhances CBF and CBD via an [Ca2+]i increase. Immunofluorescence and immunoblotting studies demonstrated that Cav1.2 and α7-nAChR are expressed in airway cilia. Moreover, IL-13 stimulated MLA-sensitive increases in CBF and CBD in airway ciliary cells, suggesting an autocrine regulation of ciliary beating by CaV1.2/α7-nAChR/ACh. In conclusion, a novel Ca2+ signalling pathway in airway cilia, CaV1.2/α7-nAChR, enhances CBF and CBD and activates mucociliary clearance maintaining healthy airways.

Keywords: Airway; Ciliary beating; Intracellular Ca2+ concentration; VDCC; α7 nicotinic acetylcholine receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine* / metabolism
  • Acetylcholine* / pharmacology
  • Animals
  • Benzamides / pharmacology
  • Bridged Bicyclo Compounds / pharmacology
  • Calcium Channel Blockers / pharmacology
  • Calcium Channels, L-Type* / metabolism
  • Cholinergic Agents / pharmacology
  • Cilia* / drug effects
  • Cilia* / physiology
  • Interleukin-13 / metabolism
  • Mice
  • Nicotinic Agonists / pharmacology
  • Nifedipine / pharmacology
  • Respiratory Mucosa* / metabolism
  • Respiratory Mucosa* / physiology
  • alpha7 Nicotinic Acetylcholine Receptor* / antagonists & inhibitors
  • alpha7 Nicotinic Acetylcholine Receptor* / metabolism

Substances

  • Benzamides
  • Bridged Bicyclo Compounds
  • CACNA1C protein, mouse
  • Calcium Channel Blockers
  • Calcium Channels, L-Type
  • Cholinergic Agents
  • Interleukin-13
  • Nicotinic Agonists
  • PNU-282987
  • alpha7 Nicotinic Acetylcholine Receptor
  • Nifedipine
  • Acetylcholine