Taste Receptors in Upper Airway Innate Immunity

Taste receptors, first identified on the tongue, are best known for their role in guiding our dietary preferences. The expression of taste receptors for umami, sweet, and bitter have been demonstrated in tissues outside of the oral cavity, including in the airway, brain, gastrointestinal tract, and...

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Main Authors: Ryan M. Carey, Robert J. Lee
Format: Article
Language:English
Published: MDPI AG 2019-08-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/11/9/2017
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spelling doaj-4f2299e27ccc41b2b3fc0f996e48692d2020-11-25T02:01:12ZengMDPI AGNutrients2072-66432019-08-01119201710.3390/nu11092017nu11092017Taste Receptors in Upper Airway Innate ImmunityRyan M. Carey0Robert J. Lee1Department of Otorhinolaryngology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USADepartment of Otorhinolaryngology and Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USATaste receptors, first identified on the tongue, are best known for their role in guiding our dietary preferences. The expression of taste receptors for umami, sweet, and bitter have been demonstrated in tissues outside of the oral cavity, including in the airway, brain, gastrointestinal tract, and reproductive organs. The extra-oral taste receptor chemosensory pathways and the endogenous taste receptor ligands are generally unknown, but there is increasing data suggesting that taste receptors are involved in regulating some aspects of innate immunity, and may potentially control the composition of the nasal microbiome in healthy individuals or patients with upper respiratory diseases like chronic rhinosinusitis (CRS). For this reason, taste receptors may serve as potential therapeutic targets, providing alternatives to conventional antibiotics. This review focuses on the physiology of sweet (T1R) and bitter (T2R) taste receptors in the airway and their activation by secreted bacterial products. There is particular focus on T2R38 in sinonasal ciliated cells, as well as the sweet and bitter receptors found on specialized sinonasal solitary chemosensory cells. Additionally, this review explores the impact of genetic variations in these receptors on the differential susceptibility of patients to upper airway infections, such as CRS.https://www.mdpi.com/2072-6643/11/9/2017chronic rhinosinusitisnitric oxideinnate immunitycilianasal diseasegustationrespiratory infectionantimicrobial peptidesmucociliary clearance
collection DOAJ
language English
format Article
sources DOAJ
author Ryan M. Carey
Robert J. Lee
spellingShingle Ryan M. Carey
Robert J. Lee
Taste Receptors in Upper Airway Innate Immunity
Nutrients
chronic rhinosinusitis
nitric oxide
innate immunity
cilia
nasal disease
gustation
respiratory infection
antimicrobial peptides
mucociliary clearance
author_facet Ryan M. Carey
Robert J. Lee
author_sort Ryan M. Carey
title Taste Receptors in Upper Airway Innate Immunity
title_short Taste Receptors in Upper Airway Innate Immunity
title_full Taste Receptors in Upper Airway Innate Immunity
title_fullStr Taste Receptors in Upper Airway Innate Immunity
title_full_unstemmed Taste Receptors in Upper Airway Innate Immunity
title_sort taste receptors in upper airway innate immunity
publisher MDPI AG
series Nutrients
issn 2072-6643
publishDate 2019-08-01
description Taste receptors, first identified on the tongue, are best known for their role in guiding our dietary preferences. The expression of taste receptors for umami, sweet, and bitter have been demonstrated in tissues outside of the oral cavity, including in the airway, brain, gastrointestinal tract, and reproductive organs. The extra-oral taste receptor chemosensory pathways and the endogenous taste receptor ligands are generally unknown, but there is increasing data suggesting that taste receptors are involved in regulating some aspects of innate immunity, and may potentially control the composition of the nasal microbiome in healthy individuals or patients with upper respiratory diseases like chronic rhinosinusitis (CRS). For this reason, taste receptors may serve as potential therapeutic targets, providing alternatives to conventional antibiotics. This review focuses on the physiology of sweet (T1R) and bitter (T2R) taste receptors in the airway and their activation by secreted bacterial products. There is particular focus on T2R38 in sinonasal ciliated cells, as well as the sweet and bitter receptors found on specialized sinonasal solitary chemosensory cells. Additionally, this review explores the impact of genetic variations in these receptors on the differential susceptibility of patients to upper airway infections, such as CRS.
topic chronic rhinosinusitis
nitric oxide
innate immunity
cilia
nasal disease
gustation
respiratory infection
antimicrobial peptides
mucociliary clearance
url https://www.mdpi.com/2072-6643/11/9/2017
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