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The Development of Cooperative Channels Explains the Maturation of Hair Cell’s Mechanotransduction

Hearing relies on the conversion of mechanical stimuli into electrical signals. In vertebrates, this process of mechanoelectrical transduction (MET) is performed by specialized receptors of the inner ear, the hair cells. Each hair cell is crowned by a hair bundle, a cluster of microvilli that pivot...

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Autores principales: Gianoli, Francesco, Risler, Thomas, Kozlov, Andrei S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817549/
https://www.ncbi.nlm.nih.gov/pubmed/31585704
http://dx.doi.org/10.1016/j.bpj.2019.08.042
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author Gianoli, Francesco
Risler, Thomas
Kozlov, Andrei S.
author_facet Gianoli, Francesco
Risler, Thomas
Kozlov, Andrei S.
author_sort Gianoli, Francesco
collection PubMed
description Hearing relies on the conversion of mechanical stimuli into electrical signals. In vertebrates, this process of mechanoelectrical transduction (MET) is performed by specialized receptors of the inner ear, the hair cells. Each hair cell is crowned by a hair bundle, a cluster of microvilli that pivot in response to sound vibrations, causing the opening and closing of mechanosensitive ion channels. Mechanical forces are projected onto the channels by molecular springs called tip links. Each tip link is thought to connect to a small number of MET channels that gate cooperatively and operate as a single transduction unit. Pushing the hair bundle in the excitatory direction opens the channels, after which they rapidly reclose in a process called fast adaptation. It has been experimentally observed that the hair cell’s biophysical properties mature gradually during postnatal development: the maximal transduction current increases, sensitivity sharpens, transduction occurs at smaller hair-bundle displacements, and adaptation becomes faster. Similar observations have been reported during tip-link regeneration after acoustic damage. Moreover, when measured at intermediate developmental stages, the kinetics of fast adaptation varies in a given cell, depending on the magnitude of the imposed displacement. The mechanisms underlying these seemingly disparate observations have so far remained elusive. Here, we show that these phenomena can all be explained by the progressive addition of MET channels of constant properties, which populate the hair bundle first as isolated entities and then progressively as clusters of more sensitive, cooperative MET channels. As the proposed mechanism relies on the difference in biophysical properties between isolated and clustered channels, this work highlights the importance of cooperative interactions between mechanosensitive ion channels for hearing.
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spelling pubmed-68175492020-10-10 The Development of Cooperative Channels Explains the Maturation of Hair Cell’s Mechanotransduction Gianoli, Francesco Risler, Thomas Kozlov, Andrei S. Biophys J Articles Hearing relies on the conversion of mechanical stimuli into electrical signals. In vertebrates, this process of mechanoelectrical transduction (MET) is performed by specialized receptors of the inner ear, the hair cells. Each hair cell is crowned by a hair bundle, a cluster of microvilli that pivot in response to sound vibrations, causing the opening and closing of mechanosensitive ion channels. Mechanical forces are projected onto the channels by molecular springs called tip links. Each tip link is thought to connect to a small number of MET channels that gate cooperatively and operate as a single transduction unit. Pushing the hair bundle in the excitatory direction opens the channels, after which they rapidly reclose in a process called fast adaptation. It has been experimentally observed that the hair cell’s biophysical properties mature gradually during postnatal development: the maximal transduction current increases, sensitivity sharpens, transduction occurs at smaller hair-bundle displacements, and adaptation becomes faster. Similar observations have been reported during tip-link regeneration after acoustic damage. Moreover, when measured at intermediate developmental stages, the kinetics of fast adaptation varies in a given cell, depending on the magnitude of the imposed displacement. The mechanisms underlying these seemingly disparate observations have so far remained elusive. Here, we show that these phenomena can all be explained by the progressive addition of MET channels of constant properties, which populate the hair bundle first as isolated entities and then progressively as clusters of more sensitive, cooperative MET channels. As the proposed mechanism relies on the difference in biophysical properties between isolated and clustered channels, this work highlights the importance of cooperative interactions between mechanosensitive ion channels for hearing. The Biophysical Society 2019-10-15 2019-09-12 /pmc/articles/PMC6817549/ /pubmed/31585704 http://dx.doi.org/10.1016/j.bpj.2019.08.042 Text en © 2019 Biophysical Society. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Articles
Gianoli, Francesco
Risler, Thomas
Kozlov, Andrei S.
The Development of Cooperative Channels Explains the Maturation of Hair Cell’s Mechanotransduction
title The Development of Cooperative Channels Explains the Maturation of Hair Cell’s Mechanotransduction
title_full The Development of Cooperative Channels Explains the Maturation of Hair Cell’s Mechanotransduction
title_fullStr The Development of Cooperative Channels Explains the Maturation of Hair Cell’s Mechanotransduction
title_full_unstemmed The Development of Cooperative Channels Explains the Maturation of Hair Cell’s Mechanotransduction
title_short The Development of Cooperative Channels Explains the Maturation of Hair Cell’s Mechanotransduction
title_sort development of cooperative channels explains the maturation of hair cell’s mechanotransduction
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817549/
https://www.ncbi.nlm.nih.gov/pubmed/31585704
http://dx.doi.org/10.1016/j.bpj.2019.08.042
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