Cargando…
Vibration hotspots reveal longitudinal funneling of sound-evoked motion in the mammalian cochlea
The micromechanical mechanisms that underpin tuning and dynamic range compression in the mammalian inner ear are fundamental to hearing, but poorly understood. Here, we present new, high-resolution optical measurements that directly map sound-evoked vibrations on to anatomical structures in the inta...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6076242/ https://www.ncbi.nlm.nih.gov/pubmed/30076297 http://dx.doi.org/10.1038/s41467-018-05483-z |
_version_ | 1783344675459956736 |
---|---|
author | Cooper, Nigel P. Vavakou, Anna van der Heijden, Marcel |
author_facet | Cooper, Nigel P. Vavakou, Anna van der Heijden, Marcel |
author_sort | Cooper, Nigel P. |
collection | PubMed |
description | The micromechanical mechanisms that underpin tuning and dynamic range compression in the mammalian inner ear are fundamental to hearing, but poorly understood. Here, we present new, high-resolution optical measurements that directly map sound-evoked vibrations on to anatomical structures in the intact, living gerbil cochlea. The largest vibrations occur in a tightly delineated hotspot centering near the interface between the Deiters’ and outer hair cells. Hotspot vibrations are less sharply tuned, but more nonlinear, than basilar membrane vibrations, and behave non-monotonically (exhibiting hyper-compression) near their characteristic frequency. Amplitude and phase differences between hotspot and basilar membrane responses depend on both frequency and measurement angle, and indicate that hotspot vibrations involve longitudinal motion. We hypothesize that structural coupling between the Deiters’ and outer hair cells funnels sound-evoked motion into the hotspot region, under the control of the outer hair cells, to optimize cochlear tuning and compression. |
format | Online Article Text |
id | pubmed-6076242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60762422018-08-07 Vibration hotspots reveal longitudinal funneling of sound-evoked motion in the mammalian cochlea Cooper, Nigel P. Vavakou, Anna van der Heijden, Marcel Nat Commun Article The micromechanical mechanisms that underpin tuning and dynamic range compression in the mammalian inner ear are fundamental to hearing, but poorly understood. Here, we present new, high-resolution optical measurements that directly map sound-evoked vibrations on to anatomical structures in the intact, living gerbil cochlea. The largest vibrations occur in a tightly delineated hotspot centering near the interface between the Deiters’ and outer hair cells. Hotspot vibrations are less sharply tuned, but more nonlinear, than basilar membrane vibrations, and behave non-monotonically (exhibiting hyper-compression) near their characteristic frequency. Amplitude and phase differences between hotspot and basilar membrane responses depend on both frequency and measurement angle, and indicate that hotspot vibrations involve longitudinal motion. We hypothesize that structural coupling between the Deiters’ and outer hair cells funnels sound-evoked motion into the hotspot region, under the control of the outer hair cells, to optimize cochlear tuning and compression. Nature Publishing Group UK 2018-08-03 /pmc/articles/PMC6076242/ /pubmed/30076297 http://dx.doi.org/10.1038/s41467-018-05483-z Text en © The Author(s) 2018 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 Cooper, Nigel P. Vavakou, Anna van der Heijden, Marcel Vibration hotspots reveal longitudinal funneling of sound-evoked motion in the mammalian cochlea |
title | Vibration hotspots reveal longitudinal funneling of sound-evoked motion in the mammalian cochlea |
title_full | Vibration hotspots reveal longitudinal funneling of sound-evoked motion in the mammalian cochlea |
title_fullStr | Vibration hotspots reveal longitudinal funneling of sound-evoked motion in the mammalian cochlea |
title_full_unstemmed | Vibration hotspots reveal longitudinal funneling of sound-evoked motion in the mammalian cochlea |
title_short | Vibration hotspots reveal longitudinal funneling of sound-evoked motion in the mammalian cochlea |
title_sort | vibration hotspots reveal longitudinal funneling of sound-evoked motion in the mammalian cochlea |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6076242/ https://www.ncbi.nlm.nih.gov/pubmed/30076297 http://dx.doi.org/10.1038/s41467-018-05483-z |
work_keys_str_mv | AT coopernigelp vibrationhotspotsreveallongitudinalfunnelingofsoundevokedmotioninthemammaliancochlea AT vavakouanna vibrationhotspotsreveallongitudinalfunnelingofsoundevokedmotioninthemammaliancochlea AT vanderheijdenmarcel vibrationhotspotsreveallongitudinalfunnelingofsoundevokedmotioninthemammaliancochlea |