Cargando…

Cochlear amplification and tuning depend on the cellular arrangement within the organ of Corti

The field of cochlear mechanics has been undergoing a revolution due to recent findings made possible by advancements in measurement techniques. While it has long been assumed that basilar-membrane (BM) motion is the most important determinant of sound transduction by the inner hair cells (IHCs), it...

Descripción completa

Detalles Bibliográficos
Autores principales: Motallebzadeh, Hamid, Soons, Joris A. M., Puria, Sunil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984506/
https://www.ncbi.nlm.nih.gov/pubmed/29760098
http://dx.doi.org/10.1073/pnas.1720979115
_version_ 1783328628823556096
author Motallebzadeh, Hamid
Soons, Joris A. M.
Puria, Sunil
author_facet Motallebzadeh, Hamid
Soons, Joris A. M.
Puria, Sunil
author_sort Motallebzadeh, Hamid
collection PubMed
description The field of cochlear mechanics has been undergoing a revolution due to recent findings made possible by advancements in measurement techniques. While it has long been assumed that basilar-membrane (BM) motion is the most important determinant of sound transduction by the inner hair cells (IHCs), it turns out that other parts of the sensory epithelium closer to the IHCs, such as the reticular lamina (RL), move with significantly greater amplitude for weaker sounds. It has not been established how these findings are related to the complex cytoarchitecture of the organ of Corti between the BM and RL, which is composed of a lattice of asymmetric Y-shaped elements, each consisting of a basally slanted outer hair cell (OHC), an apically slanted phalangeal process (PhP), and a supporting Deiters’ cell (DC). Here, a computational model of the mouse cochlea supports the hypothesis that the OHC micromotors require this Y-shaped geometry for their contribution to the exquisite sensitivity and frequency selectivity of the mammalian cochlea. By varying only the OHC gain parameter, the model can reproduce measurements of BM and RL gain and tuning for a variety of input sound levels. Malformations such as reversing the orientations of the OHCs and PhPs or removing the PhPs altogether greatly reduce the effectiveness of the OHC motors. These results imply that the DCs and PhPs must be properly accounted for in emerging OHC regeneration therapies.
format Online
Article
Text
id pubmed-5984506
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-59845062018-06-07 Cochlear amplification and tuning depend on the cellular arrangement within the organ of Corti Motallebzadeh, Hamid Soons, Joris A. M. Puria, Sunil Proc Natl Acad Sci U S A Biological Sciences The field of cochlear mechanics has been undergoing a revolution due to recent findings made possible by advancements in measurement techniques. While it has long been assumed that basilar-membrane (BM) motion is the most important determinant of sound transduction by the inner hair cells (IHCs), it turns out that other parts of the sensory epithelium closer to the IHCs, such as the reticular lamina (RL), move with significantly greater amplitude for weaker sounds. It has not been established how these findings are related to the complex cytoarchitecture of the organ of Corti between the BM and RL, which is composed of a lattice of asymmetric Y-shaped elements, each consisting of a basally slanted outer hair cell (OHC), an apically slanted phalangeal process (PhP), and a supporting Deiters’ cell (DC). Here, a computational model of the mouse cochlea supports the hypothesis that the OHC micromotors require this Y-shaped geometry for their contribution to the exquisite sensitivity and frequency selectivity of the mammalian cochlea. By varying only the OHC gain parameter, the model can reproduce measurements of BM and RL gain and tuning for a variety of input sound levels. Malformations such as reversing the orientations of the OHCs and PhPs or removing the PhPs altogether greatly reduce the effectiveness of the OHC motors. These results imply that the DCs and PhPs must be properly accounted for in emerging OHC regeneration therapies. National Academy of Sciences 2018-05-29 2018-05-14 /pmc/articles/PMC5984506/ /pubmed/29760098 http://dx.doi.org/10.1073/pnas.1720979115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Motallebzadeh, Hamid
Soons, Joris A. M.
Puria, Sunil
Cochlear amplification and tuning depend on the cellular arrangement within the organ of Corti
title Cochlear amplification and tuning depend on the cellular arrangement within the organ of Corti
title_full Cochlear amplification and tuning depend on the cellular arrangement within the organ of Corti
title_fullStr Cochlear amplification and tuning depend on the cellular arrangement within the organ of Corti
title_full_unstemmed Cochlear amplification and tuning depend on the cellular arrangement within the organ of Corti
title_short Cochlear amplification and tuning depend on the cellular arrangement within the organ of Corti
title_sort cochlear amplification and tuning depend on the cellular arrangement within the organ of corti
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984506/
https://www.ncbi.nlm.nih.gov/pubmed/29760098
http://dx.doi.org/10.1073/pnas.1720979115
work_keys_str_mv AT motallebzadehhamid cochlearamplificationandtuningdependonthecellulararrangementwithintheorganofcorti
AT soonsjorisam cochlearamplificationandtuningdependonthecellulararrangementwithintheorganofcorti
AT puriasunil cochlearamplificationandtuningdependonthecellulararrangementwithintheorganofcorti