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Hair bundles of cochlear outer hair cells are shaped to minimize their fluid-dynamic resistance
The mammalian sense of hearing relies on two types of sensory cells: inner hair cells transmit the auditory stimulus to the brain, while outer hair cells mechanically modulate the stimulus through active feedback. Stimulation of a hair cell is mediated by displacements of its mechanosensitive hair b...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472565/ https://www.ncbi.nlm.nih.gov/pubmed/28620181 http://dx.doi.org/10.1038/s41598-017-03773-y |
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author | Ciganović, Nikola Wolde-Kidan, Amanuel Reichenbach, Tobias |
author_facet | Ciganović, Nikola Wolde-Kidan, Amanuel Reichenbach, Tobias |
author_sort | Ciganović, Nikola |
collection | PubMed |
description | The mammalian sense of hearing relies on two types of sensory cells: inner hair cells transmit the auditory stimulus to the brain, while outer hair cells mechanically modulate the stimulus through active feedback. Stimulation of a hair cell is mediated by displacements of its mechanosensitive hair bundle which protrudes from the apical surface of the cell into a narrow fluid-filled space between reticular lamina and tectorial membrane. While hair bundles of inner hair cells are of linear shape, those of outer hair cells exhibit a distinctive V-shape. The biophysical rationale behind this morphology, however, remains unknown. Here we use analytical and computational methods to study the fluid flow across rows of differently shaped hair bundles. We find that rows of V-shaped hair bundles have a considerably reduced resistance to crossflow, and that the biologically observed shapes of hair bundles of outer hair cells are near-optimal in this regard. This observation accords with the function of outer hair cells and lends support to the recent hypothesis that inner hair cells are stimulated by a net flow, in addition to the well-established shear flow that arises from shearing between the reticular lamina and the tectorial membrane. |
format | Online Article Text |
id | pubmed-5472565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54725652017-06-19 Hair bundles of cochlear outer hair cells are shaped to minimize their fluid-dynamic resistance Ciganović, Nikola Wolde-Kidan, Amanuel Reichenbach, Tobias Sci Rep Article The mammalian sense of hearing relies on two types of sensory cells: inner hair cells transmit the auditory stimulus to the brain, while outer hair cells mechanically modulate the stimulus through active feedback. Stimulation of a hair cell is mediated by displacements of its mechanosensitive hair bundle which protrudes from the apical surface of the cell into a narrow fluid-filled space between reticular lamina and tectorial membrane. While hair bundles of inner hair cells are of linear shape, those of outer hair cells exhibit a distinctive V-shape. The biophysical rationale behind this morphology, however, remains unknown. Here we use analytical and computational methods to study the fluid flow across rows of differently shaped hair bundles. We find that rows of V-shaped hair bundles have a considerably reduced resistance to crossflow, and that the biologically observed shapes of hair bundles of outer hair cells are near-optimal in this regard. This observation accords with the function of outer hair cells and lends support to the recent hypothesis that inner hair cells are stimulated by a net flow, in addition to the well-established shear flow that arises from shearing between the reticular lamina and the tectorial membrane. Nature Publishing Group UK 2017-06-15 /pmc/articles/PMC5472565/ /pubmed/28620181 http://dx.doi.org/10.1038/s41598-017-03773-y Text en © The Author(s) 2017 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/. |
spellingShingle | Article Ciganović, Nikola Wolde-Kidan, Amanuel Reichenbach, Tobias Hair bundles of cochlear outer hair cells are shaped to minimize their fluid-dynamic resistance |
title | Hair bundles of cochlear outer hair cells are shaped to minimize their fluid-dynamic resistance |
title_full | Hair bundles of cochlear outer hair cells are shaped to minimize their fluid-dynamic resistance |
title_fullStr | Hair bundles of cochlear outer hair cells are shaped to minimize their fluid-dynamic resistance |
title_full_unstemmed | Hair bundles of cochlear outer hair cells are shaped to minimize their fluid-dynamic resistance |
title_short | Hair bundles of cochlear outer hair cells are shaped to minimize their fluid-dynamic resistance |
title_sort | hair bundles of cochlear outer hair cells are shaped to minimize their fluid-dynamic resistance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472565/ https://www.ncbi.nlm.nih.gov/pubmed/28620181 http://dx.doi.org/10.1038/s41598-017-03773-y |
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