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The Complex Journey of the Calcium Regulation Downstream of TAS2R Activation

Bitter taste receptors (TAS2Rs) have recently arisen as a potential drug target for asthma due to their localization in airway cells. These receptors are expressed in all cell types of the respiratory system comprising epithelial, smooth muscle and immune cells; however, the expression pattern of th...

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Detalles Bibliográficos
Autores principales: Talmon, Maria, Pollastro, Federica, Fresu, Luigia Grazia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688576/
https://www.ncbi.nlm.nih.gov/pubmed/36429066
http://dx.doi.org/10.3390/cells11223638
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author Talmon, Maria
Pollastro, Federica
Fresu, Luigia Grazia
author_facet Talmon, Maria
Pollastro, Federica
Fresu, Luigia Grazia
author_sort Talmon, Maria
collection PubMed
description Bitter taste receptors (TAS2Rs) have recently arisen as a potential drug target for asthma due to their localization in airway cells. These receptors are expressed in all cell types of the respiratory system comprising epithelial, smooth muscle and immune cells; however, the expression pattern of the subtypes is different in each cell type and, accordingly, so is their role, for example, anti-inflammatory or bronchodilator. The most challenging aspect in studying TAS2Rs has been the identification of the downstream signaling cascades. Indeed, TAS2R activation leads to canonical IP3-dependent calcium release from the ER, but, alongside, there are other mechanisms that differ according to the histological localization. In this review, we summarize the current knowledge on the cytosolic calcium modulation downstream of TAS2R activation in the epithelial, smooth muscle and immune cells of the airway system.
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spelling pubmed-96885762022-11-25 The Complex Journey of the Calcium Regulation Downstream of TAS2R Activation Talmon, Maria Pollastro, Federica Fresu, Luigia Grazia Cells Review Bitter taste receptors (TAS2Rs) have recently arisen as a potential drug target for asthma due to their localization in airway cells. These receptors are expressed in all cell types of the respiratory system comprising epithelial, smooth muscle and immune cells; however, the expression pattern of the subtypes is different in each cell type and, accordingly, so is their role, for example, anti-inflammatory or bronchodilator. The most challenging aspect in studying TAS2Rs has been the identification of the downstream signaling cascades. Indeed, TAS2R activation leads to canonical IP3-dependent calcium release from the ER, but, alongside, there are other mechanisms that differ according to the histological localization. In this review, we summarize the current knowledge on the cytosolic calcium modulation downstream of TAS2R activation in the epithelial, smooth muscle and immune cells of the airway system. MDPI 2022-11-16 /pmc/articles/PMC9688576/ /pubmed/36429066 http://dx.doi.org/10.3390/cells11223638 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Talmon, Maria
Pollastro, Federica
Fresu, Luigia Grazia
The Complex Journey of the Calcium Regulation Downstream of TAS2R Activation
title The Complex Journey of the Calcium Regulation Downstream of TAS2R Activation
title_full The Complex Journey of the Calcium Regulation Downstream of TAS2R Activation
title_fullStr The Complex Journey of the Calcium Regulation Downstream of TAS2R Activation
title_full_unstemmed The Complex Journey of the Calcium Regulation Downstream of TAS2R Activation
title_short The Complex Journey of the Calcium Regulation Downstream of TAS2R Activation
title_sort complex journey of the calcium regulation downstream of tas2r activation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688576/
https://www.ncbi.nlm.nih.gov/pubmed/36429066
http://dx.doi.org/10.3390/cells11223638
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