Normal hearing sensitivity at low-to-middle frequencies with 34% prestin-charge density.

The mammalian outer hair cells (OHCs) provide a positive mechanical feedback to enhance the cochlea's hearing sensitivity and frequency selectivity. Although the OHC-specific, somatic motor protein prestin is required for cochlear amplification, it remains unclear whether prestin can provide su...

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Main Authors: Tetsuji Yamashita, Jie Fang, Jiangang Gao, Yiling Yu, Marcia Mellado Lagarde, Jian Zuo
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3448665?pdf=render
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spelling doaj-8e436fbbdefc4257ad4d5837f6a0a75e2020-11-24T22:17:06ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0179e4545310.1371/journal.pone.0045453Normal hearing sensitivity at low-to-middle frequencies with 34% prestin-charge density.Tetsuji YamashitaJie FangJiangang GaoYiling YuMarcia Mellado LagardeJian ZuoThe mammalian outer hair cells (OHCs) provide a positive mechanical feedback to enhance the cochlea's hearing sensitivity and frequency selectivity. Although the OHC-specific, somatic motor protein prestin is required for cochlear amplification, it remains unclear whether prestin can provide sufficient cycle-by-cycle feedback. In cochlear mechanical modeling, varying amounts of OHC motor activity should provide varying degrees of feedback efficiency to adjust the gain of cochlear amplifier at resonant frequencies. Here we created and characterized two new prestin-hypomorphic mouse models with reduced levels of wild-type prestin. OHCs from these mice exhibited length, total elementary charge movement (Q(max)), charge density, and electromotility intermediate between those of wild-type and prestin-null mice. Remarkably, measurements of auditory brainstem responses and distortion product otoacoustic emissions from these mice displayed wild-type like hearing sensitivities at 4-22 kHz. These results indicate that as low as 26.7% Q(max), 34.0% charge density and 44.0% electromotility in OHCs were sufficient for wild-type-like hearing sensitivity in mice at 4-22 kHz, and that these in vitro parameters of OHCs did not correlate linearly with the feedback efficiency for in vivo gain of the cochlear amplifier. Our results thus provide valuable data for modeling cochlear mechanics and will stimulate further mechanistic analysis of the cochlear amplifier.http://europepmc.org/articles/PMC3448665?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Tetsuji Yamashita
Jie Fang
Jiangang Gao
Yiling Yu
Marcia Mellado Lagarde
Jian Zuo
spellingShingle Tetsuji Yamashita
Jie Fang
Jiangang Gao
Yiling Yu
Marcia Mellado Lagarde
Jian Zuo
Normal hearing sensitivity at low-to-middle frequencies with 34% prestin-charge density.
PLoS ONE
author_facet Tetsuji Yamashita
Jie Fang
Jiangang Gao
Yiling Yu
Marcia Mellado Lagarde
Jian Zuo
author_sort Tetsuji Yamashita
title Normal hearing sensitivity at low-to-middle frequencies with 34% prestin-charge density.
title_short Normal hearing sensitivity at low-to-middle frequencies with 34% prestin-charge density.
title_full Normal hearing sensitivity at low-to-middle frequencies with 34% prestin-charge density.
title_fullStr Normal hearing sensitivity at low-to-middle frequencies with 34% prestin-charge density.
title_full_unstemmed Normal hearing sensitivity at low-to-middle frequencies with 34% prestin-charge density.
title_sort normal hearing sensitivity at low-to-middle frequencies with 34% prestin-charge density.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The mammalian outer hair cells (OHCs) provide a positive mechanical feedback to enhance the cochlea's hearing sensitivity and frequency selectivity. Although the OHC-specific, somatic motor protein prestin is required for cochlear amplification, it remains unclear whether prestin can provide sufficient cycle-by-cycle feedback. In cochlear mechanical modeling, varying amounts of OHC motor activity should provide varying degrees of feedback efficiency to adjust the gain of cochlear amplifier at resonant frequencies. Here we created and characterized two new prestin-hypomorphic mouse models with reduced levels of wild-type prestin. OHCs from these mice exhibited length, total elementary charge movement (Q(max)), charge density, and electromotility intermediate between those of wild-type and prestin-null mice. Remarkably, measurements of auditory brainstem responses and distortion product otoacoustic emissions from these mice displayed wild-type like hearing sensitivities at 4-22 kHz. These results indicate that as low as 26.7% Q(max), 34.0% charge density and 44.0% electromotility in OHCs were sufficient for wild-type-like hearing sensitivity in mice at 4-22 kHz, and that these in vitro parameters of OHCs did not correlate linearly with the feedback efficiency for in vivo gain of the cochlear amplifier. Our results thus provide valuable data for modeling cochlear mechanics and will stimulate further mechanistic analysis of the cochlear amplifier.
url http://europepmc.org/articles/PMC3448665?pdf=render
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