4.6 Article

Taste Receptor Activation in Tracheal Brush Cells by Denatonium Modulates ENaC Channels via Ca2+, cAMP and ACh

Journal

CELLS
Volume 11, Issue 15, Pages -

Publisher

MDPI
DOI: 10.3390/cells11152411

Keywords

ion transport; airway epithelium; Ussing chamber; mucociliary clearance; brush cell; ENaC; ACh; Trpm5; CFTR

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Funding

  1. German Research Foundation (DFG) [SFB TRR152, 2338, KR4338/1-2]
  2. Homfor2022 (Homburger Forschungsforderung, Saarland University)

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This study found that brush cells play a regulatory role in mucociliary clearance in the airways. Activation of brush cells leads to the inhibition of epithelial sodium channels through the bitter taste signaling cascade, resulting in a reduction of mucociliary clearance.
Mucociliary clearance is a primary defence mechanism of the airways consisting of two components, ciliary beating and transepithelial ion transport (I-SC). Specialised chemosensory cholinergic epithelial cells, named brush cells (BC), are involved in regulating various physiological and immunological processes. However, it remains unclear if BC influence I-SC. In murine tracheae, denatonium, a taste receptor agonist, reduced basal I-SC in a concentration-dependent manner (EC50 397 mu M). The inhibition of bitter taste signalling components with gallein (G(beta gamma) subunits), U73122 (phospholipase C), 2-APB (IP3-receptors) or with TPPO (Trpm5, transient receptor potential-melastatin 5 channel) reduced the denatonium effect. Supportively, the I-SC was also diminished in Trpm5(-/-) mice. Mecamylamine (nicotinic acetylcholine receptor, nAChR, inhibitor) and amiloride (epithelial sodium channel, ENaC, antagonist) decreased the denatonium effect. Additionally, the inhibition of G(alpha) subunits (pertussis toxin) reduced the denatonium effect, while an inhibition of phosphodiesterase (IBMX) increased and of adenylate cyclase (forskolin) reversed the denatonium effect. The cystic fibrosis transmembrane conductance regulator (CFTR) inhibitor CFTRinh172 and the KCNQ1 potassium channel antagonist chromanol 293B both reduced the denatonium effect. Thus, denatonium reduces I-SC via the canonical bitter taste signalling cascade leading to the Trpm5-dependent nAChR-mediated inhibition of ENaC as well as G(alpha) signalling leading to a reduction in cAMP-dependent I-SC. Therefore, BC activation contributes to the regulation of fluid homeostasis.

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