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In situ motions of individual inner-hair-cell stereocilia from stapes stimulation in adult mice

In vertebrate hearing organs, mechanical vibrations are converted to ionic currents through mechanoelectrical-transduction (MET) channels. Concerted stereocilia motion produces an ensemble MET current driving the hair-cell receptor potential. Mammalian cochleae are unique in that the tuning of senso...

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Autores principales: Wang, Yanli, Steele, Charles R., Puria, Sunil, Ricci, Anthony J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357788/
https://www.ncbi.nlm.nih.gov/pubmed/34381157
http://dx.doi.org/10.1038/s42003-021-02459-6
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author Wang, Yanli
Steele, Charles R.
Puria, Sunil
Ricci, Anthony J.
author_facet Wang, Yanli
Steele, Charles R.
Puria, Sunil
Ricci, Anthony J.
author_sort Wang, Yanli
collection PubMed
description In vertebrate hearing organs, mechanical vibrations are converted to ionic currents through mechanoelectrical-transduction (MET) channels. Concerted stereocilia motion produces an ensemble MET current driving the hair-cell receptor potential. Mammalian cochleae are unique in that the tuning of sensory cells is determined by their mechanical environment and the mode of hair-bundle stimulation that their environment creates. However, little is known about the in situ intra-hair-bundle motions of stereocilia relative to one another, or to their environment. In this study, high-speed imaging allowed the stereocilium and cell-body motions of inner hair cells to be monitored in an ex vivo organ of Corti (OoC) mouse preparation. We have found that the OoC rotates about the base of the inner pillar cell, the hair bundle rotates about its base and lags behind the motion of the apical surface of the cell, and the individual stereocilia move semi-independently within a given hair bundle.
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spelling pubmed-83577882021-08-30 In situ motions of individual inner-hair-cell stereocilia from stapes stimulation in adult mice Wang, Yanli Steele, Charles R. Puria, Sunil Ricci, Anthony J. Commun Biol Article In vertebrate hearing organs, mechanical vibrations are converted to ionic currents through mechanoelectrical-transduction (MET) channels. Concerted stereocilia motion produces an ensemble MET current driving the hair-cell receptor potential. Mammalian cochleae are unique in that the tuning of sensory cells is determined by their mechanical environment and the mode of hair-bundle stimulation that their environment creates. However, little is known about the in situ intra-hair-bundle motions of stereocilia relative to one another, or to their environment. In this study, high-speed imaging allowed the stereocilium and cell-body motions of inner hair cells to be monitored in an ex vivo organ of Corti (OoC) mouse preparation. We have found that the OoC rotates about the base of the inner pillar cell, the hair bundle rotates about its base and lags behind the motion of the apical surface of the cell, and the individual stereocilia move semi-independently within a given hair bundle. Nature Publishing Group UK 2021-08-11 /pmc/articles/PMC8357788/ /pubmed/34381157 http://dx.doi.org/10.1038/s42003-021-02459-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Yanli
Steele, Charles R.
Puria, Sunil
Ricci, Anthony J.
In situ motions of individual inner-hair-cell stereocilia from stapes stimulation in adult mice
title In situ motions of individual inner-hair-cell stereocilia from stapes stimulation in adult mice
title_full In situ motions of individual inner-hair-cell stereocilia from stapes stimulation in adult mice
title_fullStr In situ motions of individual inner-hair-cell stereocilia from stapes stimulation in adult mice
title_full_unstemmed In situ motions of individual inner-hair-cell stereocilia from stapes stimulation in adult mice
title_short In situ motions of individual inner-hair-cell stereocilia from stapes stimulation in adult mice
title_sort in situ motions of individual inner-hair-cell stereocilia from stapes stimulation in adult mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357788/
https://www.ncbi.nlm.nih.gov/pubmed/34381157
http://dx.doi.org/10.1038/s42003-021-02459-6
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