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Volume electron microscopy reveals age-related circuit remodeling in the auditory brainstem
The medial nucleus of the trapezoid body (MNTB) is an integral component of the auditory brainstem circuitry involved in sound localization. The giant presynaptic nerve terminal with multiple active zones, the calyx of Held (CH), is a hallmark of this nucleus, which mediates fast and synchronized gl...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9799098/ https://www.ncbi.nlm.nih.gov/pubmed/36589288 http://dx.doi.org/10.3389/fncel.2022.1070438 |
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author | Chequer Charan, Daniela Hua, Yunfeng Wang, Haoyu Huang, Wenqing Wang, Fangfang Elgoyhen, Ana Belén Boergens, Kevin M. Di Guilmi, Mariano N. |
author_facet | Chequer Charan, Daniela Hua, Yunfeng Wang, Haoyu Huang, Wenqing Wang, Fangfang Elgoyhen, Ana Belén Boergens, Kevin M. Di Guilmi, Mariano N. |
author_sort | Chequer Charan, Daniela |
collection | PubMed |
description | The medial nucleus of the trapezoid body (MNTB) is an integral component of the auditory brainstem circuitry involved in sound localization. The giant presynaptic nerve terminal with multiple active zones, the calyx of Held (CH), is a hallmark of this nucleus, which mediates fast and synchronized glutamatergic synaptic transmission. To delineate how these synaptic structures adapt to reduced auditory afferents due to aging, we acquired and reconstructed circuitry-level volumes of mouse MNTB at different ages (3 weeks, 6, 18, and 24 months) using serial block-face electron microscopy. We used C57BL/6J, the most widely inbred mouse strain used for transgenic lines, which displays a type of age-related hearing loss. We found that MNTB neurons reduce in density with age. Surprisingly we observed an average of approximately 10% of poly-innervated MNTB neurons along the mouse lifespan, with prevalence in the low frequency region. Moreover, a tonotopy-dependent heterogeneity in CH morphology was observed in young but not in older mice. In conclusion, our data support the notion that age-related hearing impairments can be in part a direct consequence of several structural alterations and circuit remodeling in the brainstem. |
format | Online Article Text |
id | pubmed-9799098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97990982022-12-30 Volume electron microscopy reveals age-related circuit remodeling in the auditory brainstem Chequer Charan, Daniela Hua, Yunfeng Wang, Haoyu Huang, Wenqing Wang, Fangfang Elgoyhen, Ana Belén Boergens, Kevin M. Di Guilmi, Mariano N. Front Cell Neurosci Cellular Neuroscience The medial nucleus of the trapezoid body (MNTB) is an integral component of the auditory brainstem circuitry involved in sound localization. The giant presynaptic nerve terminal with multiple active zones, the calyx of Held (CH), is a hallmark of this nucleus, which mediates fast and synchronized glutamatergic synaptic transmission. To delineate how these synaptic structures adapt to reduced auditory afferents due to aging, we acquired and reconstructed circuitry-level volumes of mouse MNTB at different ages (3 weeks, 6, 18, and 24 months) using serial block-face electron microscopy. We used C57BL/6J, the most widely inbred mouse strain used for transgenic lines, which displays a type of age-related hearing loss. We found that MNTB neurons reduce in density with age. Surprisingly we observed an average of approximately 10% of poly-innervated MNTB neurons along the mouse lifespan, with prevalence in the low frequency region. Moreover, a tonotopy-dependent heterogeneity in CH morphology was observed in young but not in older mice. In conclusion, our data support the notion that age-related hearing impairments can be in part a direct consequence of several structural alterations and circuit remodeling in the brainstem. Frontiers Media S.A. 2022-12-15 /pmc/articles/PMC9799098/ /pubmed/36589288 http://dx.doi.org/10.3389/fncel.2022.1070438 Text en Copyright © 2022 Chequer Charan, Hua, Wang, Huang, Wang, Elgoyhen, Boergens and Di Guilmi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular Neuroscience Chequer Charan, Daniela Hua, Yunfeng Wang, Haoyu Huang, Wenqing Wang, Fangfang Elgoyhen, Ana Belén Boergens, Kevin M. Di Guilmi, Mariano N. Volume electron microscopy reveals age-related circuit remodeling in the auditory brainstem |
title | Volume electron microscopy reveals age-related circuit remodeling in the auditory brainstem |
title_full | Volume electron microscopy reveals age-related circuit remodeling in the auditory brainstem |
title_fullStr | Volume electron microscopy reveals age-related circuit remodeling in the auditory brainstem |
title_full_unstemmed | Volume electron microscopy reveals age-related circuit remodeling in the auditory brainstem |
title_short | Volume electron microscopy reveals age-related circuit remodeling in the auditory brainstem |
title_sort | volume electron microscopy reveals age-related circuit remodeling in the auditory brainstem |
topic | Cellular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9799098/ https://www.ncbi.nlm.nih.gov/pubmed/36589288 http://dx.doi.org/10.3389/fncel.2022.1070438 |
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