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Mechanisms of PIEZO Channel Inactivation

PIEZO channels PIEZO1 and PIEZO2 are the newly identified mechanosensitive, non-selective cation channels permeable to Ca(2+). In higher vertebrates, PIEZO1 is expressed ubiquitously in most tissues and cells while PIEZO2 is expressed more specifically in the peripheral sensory neurons. PIEZO channe...

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Detalles Bibliográficos
Autores principales: Zhou, Zijing, Martinac, Boris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531961/
https://www.ncbi.nlm.nih.gov/pubmed/37762415
http://dx.doi.org/10.3390/ijms241814113
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author Zhou, Zijing
Martinac, Boris
author_facet Zhou, Zijing
Martinac, Boris
author_sort Zhou, Zijing
collection PubMed
description PIEZO channels PIEZO1 and PIEZO2 are the newly identified mechanosensitive, non-selective cation channels permeable to Ca(2+). In higher vertebrates, PIEZO1 is expressed ubiquitously in most tissues and cells while PIEZO2 is expressed more specifically in the peripheral sensory neurons. PIEZO channels contribute to a wide range of biological behaviors and developmental processes, therefore driving significant attention in the effort to understand their molecular properties. One prominent property of PIEZO channels is their rapid inactivation, which manifests itself as a decrease in channel open probability in the presence of a sustained mechanical stimulus. The lack of the PIEZO channel inactivation is linked to various mechanopathologies emphasizing the significance of studying this PIEZO channel property and the factors affecting it. In the present review, we discuss the mechanisms underlying the PIEZO channel inactivation, its modulation by the interaction of the channels with lipids and/or proteins, and how the changes in PIEZO inactivation by the channel mutations can cause a variety of diseases in animals and humans.
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spelling pubmed-105319612023-09-28 Mechanisms of PIEZO Channel Inactivation Zhou, Zijing Martinac, Boris Int J Mol Sci Review PIEZO channels PIEZO1 and PIEZO2 are the newly identified mechanosensitive, non-selective cation channels permeable to Ca(2+). In higher vertebrates, PIEZO1 is expressed ubiquitously in most tissues and cells while PIEZO2 is expressed more specifically in the peripheral sensory neurons. PIEZO channels contribute to a wide range of biological behaviors and developmental processes, therefore driving significant attention in the effort to understand their molecular properties. One prominent property of PIEZO channels is their rapid inactivation, which manifests itself as a decrease in channel open probability in the presence of a sustained mechanical stimulus. The lack of the PIEZO channel inactivation is linked to various mechanopathologies emphasizing the significance of studying this PIEZO channel property and the factors affecting it. In the present review, we discuss the mechanisms underlying the PIEZO channel inactivation, its modulation by the interaction of the channels with lipids and/or proteins, and how the changes in PIEZO inactivation by the channel mutations can cause a variety of diseases in animals and humans. MDPI 2023-09-14 /pmc/articles/PMC10531961/ /pubmed/37762415 http://dx.doi.org/10.3390/ijms241814113 Text en © 2023 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
Zhou, Zijing
Martinac, Boris
Mechanisms of PIEZO Channel Inactivation
title Mechanisms of PIEZO Channel Inactivation
title_full Mechanisms of PIEZO Channel Inactivation
title_fullStr Mechanisms of PIEZO Channel Inactivation
title_full_unstemmed Mechanisms of PIEZO Channel Inactivation
title_short Mechanisms of PIEZO Channel Inactivation
title_sort mechanisms of piezo channel inactivation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531961/
https://www.ncbi.nlm.nih.gov/pubmed/37762415
http://dx.doi.org/10.3390/ijms241814113
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