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Optimal Electrical Properties of Outer Hair Cells Ensure Cochlear Amplification

The organ of Corti (OC) is the auditory epithelium of the mammalian cochlea comprising sensory hair cells and supporting cells riding on the basilar membrane. The outer hair cells (OHCs) are cellular actuators that amplify small sound-induced vibrations for transmission to the inner hair cells. We d...

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Detalles Bibliográficos
Autores principales: Nam, Jong-Hoon, Fettiplace, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507780/
https://www.ncbi.nlm.nih.gov/pubmed/23209783
http://dx.doi.org/10.1371/journal.pone.0050572
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author Nam, Jong-Hoon
Fettiplace, Robert
author_facet Nam, Jong-Hoon
Fettiplace, Robert
author_sort Nam, Jong-Hoon
collection PubMed
description The organ of Corti (OC) is the auditory epithelium of the mammalian cochlea comprising sensory hair cells and supporting cells riding on the basilar membrane. The outer hair cells (OHCs) are cellular actuators that amplify small sound-induced vibrations for transmission to the inner hair cells. We developed a finite element model of the OC that incorporates the complex OC geometry and force generation by OHCs originating from active hair bundle motion due to gating of the transducer channels and somatic contractility due to the membrane protein prestin. The model also incorporates realistic OHC electrical properties. It explains the complex vibration modes of the OC and reproduces recent measurements of the phase difference between the top and the bottom surface vibrations of the OC. Simulations of an individual OHC show that the OHC somatic motility lags the hair bundle displacement by ∼90 degrees. Prestin-driven contractions of the OHCs cause the top and bottom surfaces of the OC to move in opposite directions. Combined with the OC mechanics, this results in ∼90 degrees phase difference between the OC top and bottom surface vibration. An appropriate electrical time constant for the OHC membrane is necessary to achieve the phase relationship between OC vibrations and OHC actuations. When the OHC electrical frequency characteristics are too high or too low, the OHCs do not exert force with the correct phase to the OC mechanics so that they cannot amplify. We conclude that the components of OHC forward and reverse transduction are crucial for setting the phase relations needed for amplification.
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spelling pubmed-35077802012-12-03 Optimal Electrical Properties of Outer Hair Cells Ensure Cochlear Amplification Nam, Jong-Hoon Fettiplace, Robert PLoS One Research Article The organ of Corti (OC) is the auditory epithelium of the mammalian cochlea comprising sensory hair cells and supporting cells riding on the basilar membrane. The outer hair cells (OHCs) are cellular actuators that amplify small sound-induced vibrations for transmission to the inner hair cells. We developed a finite element model of the OC that incorporates the complex OC geometry and force generation by OHCs originating from active hair bundle motion due to gating of the transducer channels and somatic contractility due to the membrane protein prestin. The model also incorporates realistic OHC electrical properties. It explains the complex vibration modes of the OC and reproduces recent measurements of the phase difference between the top and the bottom surface vibrations of the OC. Simulations of an individual OHC show that the OHC somatic motility lags the hair bundle displacement by ∼90 degrees. Prestin-driven contractions of the OHCs cause the top and bottom surfaces of the OC to move in opposite directions. Combined with the OC mechanics, this results in ∼90 degrees phase difference between the OC top and bottom surface vibration. An appropriate electrical time constant for the OHC membrane is necessary to achieve the phase relationship between OC vibrations and OHC actuations. When the OHC electrical frequency characteristics are too high or too low, the OHCs do not exert force with the correct phase to the OC mechanics so that they cannot amplify. We conclude that the components of OHC forward and reverse transduction are crucial for setting the phase relations needed for amplification. Public Library of Science 2012-11-27 /pmc/articles/PMC3507780/ /pubmed/23209783 http://dx.doi.org/10.1371/journal.pone.0050572 Text en © 2012 Nam, Fettiplace http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Nam, Jong-Hoon
Fettiplace, Robert
Optimal Electrical Properties of Outer Hair Cells Ensure Cochlear Amplification
title Optimal Electrical Properties of Outer Hair Cells Ensure Cochlear Amplification
title_full Optimal Electrical Properties of Outer Hair Cells Ensure Cochlear Amplification
title_fullStr Optimal Electrical Properties of Outer Hair Cells Ensure Cochlear Amplification
title_full_unstemmed Optimal Electrical Properties of Outer Hair Cells Ensure Cochlear Amplification
title_short Optimal Electrical Properties of Outer Hair Cells Ensure Cochlear Amplification
title_sort optimal electrical properties of outer hair cells ensure cochlear amplification
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507780/
https://www.ncbi.nlm.nih.gov/pubmed/23209783
http://dx.doi.org/10.1371/journal.pone.0050572
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