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Ultrastructure of noise-induced cochlear synaptopathy

Acoustic overexposure can eliminate synapses between inner hair cells (IHCs) and auditory nerve fibers (ANFs), even if hair-cell function recovers. This synaptopathy has been extensively studied by confocal microscopy, however, understanding the nature and sequence of damage requires ultrastructural...

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Autores principales: Moverman, Daniel J., Liberman, Leslie D., Kraemer, Stephan, Corfas, Gabriel, Liberman, M. Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636047/
https://www.ncbi.nlm.nih.gov/pubmed/37945811
http://dx.doi.org/10.1038/s41598-023-46859-6
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author Moverman, Daniel J.
Liberman, Leslie D.
Kraemer, Stephan
Corfas, Gabriel
Liberman, M. Charles
author_facet Moverman, Daniel J.
Liberman, Leslie D.
Kraemer, Stephan
Corfas, Gabriel
Liberman, M. Charles
author_sort Moverman, Daniel J.
collection PubMed
description Acoustic overexposure can eliminate synapses between inner hair cells (IHCs) and auditory nerve fibers (ANFs), even if hair-cell function recovers. This synaptopathy has been extensively studied by confocal microscopy, however, understanding the nature and sequence of damage requires ultrastructural analysis. Here, we used focused ion-beam scanning electron microscopy to mill, image, segment and reconstruct ANF terminals in mice, 1 day and 1 week after synaptopathic exposure (8–16 kHz, 98 dB SPL). At both survivals, ANF terminals were normal in number, but 62% and 53%, respectively, lacked normal synaptic specializations. Most non-synapsing fibers (57% and 48% at 1 day and 1 week) remained in contact with an IHC and contained healthy-looking organelles. ANFs showed a transient increase in mitochondrial content (51%) and efferent innervation (34%) at 1 day. Fibers maintaining synaptic connections showed hypertrophy of pre-synaptic ribbons at both 1 day and 1 week. Non-synaptic fibers were lower in mitochondrial content and typically on the modiolar side of the IHC, where ANFs with high-thresholds and low spontaneous rates are normally found. Even 1 week post-exposure, many ANF terminals remained in IHC contact despite loss of synaptic specializations, thus, regeneration efforts at early post-exposure times should concentrate on synaptogenesis rather than neurite extension.
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spelling pubmed-106360472023-11-11 Ultrastructure of noise-induced cochlear synaptopathy Moverman, Daniel J. Liberman, Leslie D. Kraemer, Stephan Corfas, Gabriel Liberman, M. Charles Sci Rep Article Acoustic overexposure can eliminate synapses between inner hair cells (IHCs) and auditory nerve fibers (ANFs), even if hair-cell function recovers. This synaptopathy has been extensively studied by confocal microscopy, however, understanding the nature and sequence of damage requires ultrastructural analysis. Here, we used focused ion-beam scanning electron microscopy to mill, image, segment and reconstruct ANF terminals in mice, 1 day and 1 week after synaptopathic exposure (8–16 kHz, 98 dB SPL). At both survivals, ANF terminals were normal in number, but 62% and 53%, respectively, lacked normal synaptic specializations. Most non-synapsing fibers (57% and 48% at 1 day and 1 week) remained in contact with an IHC and contained healthy-looking organelles. ANFs showed a transient increase in mitochondrial content (51%) and efferent innervation (34%) at 1 day. Fibers maintaining synaptic connections showed hypertrophy of pre-synaptic ribbons at both 1 day and 1 week. Non-synaptic fibers were lower in mitochondrial content and typically on the modiolar side of the IHC, where ANFs with high-thresholds and low spontaneous rates are normally found. Even 1 week post-exposure, many ANF terminals remained in IHC contact despite loss of synaptic specializations, thus, regeneration efforts at early post-exposure times should concentrate on synaptogenesis rather than neurite extension. Nature Publishing Group UK 2023-11-09 /pmc/articles/PMC10636047/ /pubmed/37945811 http://dx.doi.org/10.1038/s41598-023-46859-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Moverman, Daniel J.
Liberman, Leslie D.
Kraemer, Stephan
Corfas, Gabriel
Liberman, M. Charles
Ultrastructure of noise-induced cochlear synaptopathy
title Ultrastructure of noise-induced cochlear synaptopathy
title_full Ultrastructure of noise-induced cochlear synaptopathy
title_fullStr Ultrastructure of noise-induced cochlear synaptopathy
title_full_unstemmed Ultrastructure of noise-induced cochlear synaptopathy
title_short Ultrastructure of noise-induced cochlear synaptopathy
title_sort ultrastructure of noise-induced cochlear synaptopathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636047/
https://www.ncbi.nlm.nih.gov/pubmed/37945811
http://dx.doi.org/10.1038/s41598-023-46859-6
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