Timing of the reticular lamina and basilar membrane vibration in living gerbil cochleae

Auditory sensory outer hair cells are thought to amplify sound-induced basilar membrane vibration through a feedback mechanism to enhance hearing sensitivity. For optimal amplification, the outer hair cell-generated force must act on the basilar membrane at an appropriate time at every cycle. Howeve...

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Main Authors: Wenxuan He, David Kemp, Tianying Ren
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2018-09-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/37625
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spelling doaj-64fd67cb6e774374a4b9eb87bdcc37e52021-05-05T16:08:09ZengeLife Sciences Publications LtdeLife2050-084X2018-09-01710.7554/eLife.37625Timing of the reticular lamina and basilar membrane vibration in living gerbil cochleaeWenxuan He0David Kemp1Tianying Ren2https://orcid.org/0000-0002-2533-7203Oregon Hearing Research Center, Department of Otolaryngology, Oregon Health & Science University, Portland, United StatesUniversity College London Ear Institute, University College London, London, United KingdomOregon Hearing Research Center, Department of Otolaryngology, Oregon Health & Science University, Portland, United StatesAuditory sensory outer hair cells are thought to amplify sound-induced basilar membrane vibration through a feedback mechanism to enhance hearing sensitivity. For optimal amplification, the outer hair cell-generated force must act on the basilar membrane at an appropriate time at every cycle. However, the temporal relationship between the outer hair cell-driven reticular lamina vibration and the basilar membrane vibration remains unclear. By measuring sub-nanometer vibrations directly from outer hair cells using a custom-built heterodyne low-coherence interferometer, we demonstrate in living gerbil cochleae that the reticular lamina vibration occurs after, not before, the basilar membrane vibration. Both tone- and click-induced responses indicate that the reticular lamina and basilar membrane vibrate in opposite directions at the cochlear base and they oscillate in phase near the best-frequency location. Our results suggest that outer hair cells enhance hearing sensitivity through a global hydromechanical mechanism, rather than through a local mechanical feedback as commonly supposed.https://elifesciences.org/articles/37625cochleacochlear amplifierouter hair cellslow-coherence interferometerreticular laminabasilar membrane
collection DOAJ
language English
format Article
sources DOAJ
author Wenxuan He
David Kemp
Tianying Ren
spellingShingle Wenxuan He
David Kemp
Tianying Ren
Timing of the reticular lamina and basilar membrane vibration in living gerbil cochleae
eLife
cochlea
cochlear amplifier
outer hair cells
low-coherence interferometer
reticular lamina
basilar membrane
author_facet Wenxuan He
David Kemp
Tianying Ren
author_sort Wenxuan He
title Timing of the reticular lamina and basilar membrane vibration in living gerbil cochleae
title_short Timing of the reticular lamina and basilar membrane vibration in living gerbil cochleae
title_full Timing of the reticular lamina and basilar membrane vibration in living gerbil cochleae
title_fullStr Timing of the reticular lamina and basilar membrane vibration in living gerbil cochleae
title_full_unstemmed Timing of the reticular lamina and basilar membrane vibration in living gerbil cochleae
title_sort timing of the reticular lamina and basilar membrane vibration in living gerbil cochleae
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2018-09-01
description Auditory sensory outer hair cells are thought to amplify sound-induced basilar membrane vibration through a feedback mechanism to enhance hearing sensitivity. For optimal amplification, the outer hair cell-generated force must act on the basilar membrane at an appropriate time at every cycle. However, the temporal relationship between the outer hair cell-driven reticular lamina vibration and the basilar membrane vibration remains unclear. By measuring sub-nanometer vibrations directly from outer hair cells using a custom-built heterodyne low-coherence interferometer, we demonstrate in living gerbil cochleae that the reticular lamina vibration occurs after, not before, the basilar membrane vibration. Both tone- and click-induced responses indicate that the reticular lamina and basilar membrane vibrate in opposite directions at the cochlear base and they oscillate in phase near the best-frequency location. Our results suggest that outer hair cells enhance hearing sensitivity through a global hydromechanical mechanism, rather than through a local mechanical feedback as commonly supposed.
topic cochlea
cochlear amplifier
outer hair cells
low-coherence interferometer
reticular lamina
basilar membrane
url https://elifesciences.org/articles/37625
work_keys_str_mv AT wenxuanhe timingofthereticularlaminaandbasilarmembranevibrationinlivinggerbilcochleae
AT davidkemp timingofthereticularlaminaandbasilarmembranevibrationinlivinggerbilcochleae
AT tianyingren timingofthereticularlaminaandbasilarmembranevibrationinlivinggerbilcochleae
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