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Ca(2+) Signaling by TRPV4 Channels in Respiratory Function and Disease

Members of the transient receptor potential (TRP) superfamily are broadly expressed in our body and contribute to multiple cellular functions. Most interestingly, the fourth member of the vanilloid family of TRP channels (TRPV4) serves different partially antagonistic functions in the respiratory sy...

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Autores principales: Rajan, Suhasini, Schremmer, Christian, Weber, Jonas, Alt, Philipp, Geiger, Fabienne, Dietrich, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067475/
https://www.ncbi.nlm.nih.gov/pubmed/33917551
http://dx.doi.org/10.3390/cells10040822
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author Rajan, Suhasini
Schremmer, Christian
Weber, Jonas
Alt, Philipp
Geiger, Fabienne
Dietrich, Alexander
author_facet Rajan, Suhasini
Schremmer, Christian
Weber, Jonas
Alt, Philipp
Geiger, Fabienne
Dietrich, Alexander
author_sort Rajan, Suhasini
collection PubMed
description Members of the transient receptor potential (TRP) superfamily are broadly expressed in our body and contribute to multiple cellular functions. Most interestingly, the fourth member of the vanilloid family of TRP channels (TRPV4) serves different partially antagonistic functions in the respiratory system. This review highlights the role of TRPV4 channels in lung fibroblasts, the lung endothelium, as well as the alveolar and bronchial epithelium, during physiological and pathophysiological mechanisms. Data available from animal models and human tissues confirm the importance of this ion channel in cellular signal transduction complexes with Ca(2+) ions as a second messenger. Moreover, TRPV4 is an excellent therapeutic target with numerous specific compounds regulating its activity in diseases, like asthma, lung fibrosis, edema, and infections.
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spelling pubmed-80674752021-04-25 Ca(2+) Signaling by TRPV4 Channels in Respiratory Function and Disease Rajan, Suhasini Schremmer, Christian Weber, Jonas Alt, Philipp Geiger, Fabienne Dietrich, Alexander Cells Review Members of the transient receptor potential (TRP) superfamily are broadly expressed in our body and contribute to multiple cellular functions. Most interestingly, the fourth member of the vanilloid family of TRP channels (TRPV4) serves different partially antagonistic functions in the respiratory system. This review highlights the role of TRPV4 channels in lung fibroblasts, the lung endothelium, as well as the alveolar and bronchial epithelium, during physiological and pathophysiological mechanisms. Data available from animal models and human tissues confirm the importance of this ion channel in cellular signal transduction complexes with Ca(2+) ions as a second messenger. Moreover, TRPV4 is an excellent therapeutic target with numerous specific compounds regulating its activity in diseases, like asthma, lung fibrosis, edema, and infections. MDPI 2021-04-06 /pmc/articles/PMC8067475/ /pubmed/33917551 http://dx.doi.org/10.3390/cells10040822 Text en © 2021 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
Rajan, Suhasini
Schremmer, Christian
Weber, Jonas
Alt, Philipp
Geiger, Fabienne
Dietrich, Alexander
Ca(2+) Signaling by TRPV4 Channels in Respiratory Function and Disease
title Ca(2+) Signaling by TRPV4 Channels in Respiratory Function and Disease
title_full Ca(2+) Signaling by TRPV4 Channels in Respiratory Function and Disease
title_fullStr Ca(2+) Signaling by TRPV4 Channels in Respiratory Function and Disease
title_full_unstemmed Ca(2+) Signaling by TRPV4 Channels in Respiratory Function and Disease
title_short Ca(2+) Signaling by TRPV4 Channels in Respiratory Function and Disease
title_sort ca(2+) signaling by trpv4 channels in respiratory function and disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067475/
https://www.ncbi.nlm.nih.gov/pubmed/33917551
http://dx.doi.org/10.3390/cells10040822
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