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Efferent feedback controls bilateral auditory spontaneous activity

In the developing auditory system, spontaneous activity generated in the cochleae propagates into the central nervous system to promote circuit formation. The effects of peripheral firing patterns on spontaneous activity in the central auditory system are not well understood. Here, we describe wide-...

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Autores principales: Wang, Yixiang, Sanghvi, Maya, Gribizis, Alexandra, Zhang, Yueyi, Song, Lei, Morley, Barbara, Barson, Daniel G., Santos-Sacchi, Joseph, Navaratnam, Dhasakumar, Crair, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079389/
https://www.ncbi.nlm.nih.gov/pubmed/33907194
http://dx.doi.org/10.1038/s41467-021-22796-8
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author Wang, Yixiang
Sanghvi, Maya
Gribizis, Alexandra
Zhang, Yueyi
Song, Lei
Morley, Barbara
Barson, Daniel G.
Santos-Sacchi, Joseph
Navaratnam, Dhasakumar
Crair, Michael
author_facet Wang, Yixiang
Sanghvi, Maya
Gribizis, Alexandra
Zhang, Yueyi
Song, Lei
Morley, Barbara
Barson, Daniel G.
Santos-Sacchi, Joseph
Navaratnam, Dhasakumar
Crair, Michael
author_sort Wang, Yixiang
collection PubMed
description In the developing auditory system, spontaneous activity generated in the cochleae propagates into the central nervous system to promote circuit formation. The effects of peripheral firing patterns on spontaneous activity in the central auditory system are not well understood. Here, we describe wide-spread bilateral coupling of spontaneous activity that coincides with the period of transient efferent modulation of inner hair cells from the brainstem medial olivocochlear system. Knocking out α9/α10 nicotinic acetylcholine receptors, a requisite part of the efferent pathway, profoundly reduces bilateral correlations. Pharmacological and chemogenetic experiments confirm that the efferent system is necessary for normal bilateral coupling. Moreover, auditory sensitivity at hearing onset is reduced in the absence of pre-hearing efferent modulation. Together, these results demonstrate how afferent and efferent pathways collectively shape spontaneous activity patterns and reveal the important role of efferents in coordinating bilateral spontaneous activity and the emergence of functional responses during the prehearing period.
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spelling pubmed-80793892021-05-11 Efferent feedback controls bilateral auditory spontaneous activity Wang, Yixiang Sanghvi, Maya Gribizis, Alexandra Zhang, Yueyi Song, Lei Morley, Barbara Barson, Daniel G. Santos-Sacchi, Joseph Navaratnam, Dhasakumar Crair, Michael Nat Commun Article In the developing auditory system, spontaneous activity generated in the cochleae propagates into the central nervous system to promote circuit formation. The effects of peripheral firing patterns on spontaneous activity in the central auditory system are not well understood. Here, we describe wide-spread bilateral coupling of spontaneous activity that coincides with the period of transient efferent modulation of inner hair cells from the brainstem medial olivocochlear system. Knocking out α9/α10 nicotinic acetylcholine receptors, a requisite part of the efferent pathway, profoundly reduces bilateral correlations. Pharmacological and chemogenetic experiments confirm that the efferent system is necessary for normal bilateral coupling. Moreover, auditory sensitivity at hearing onset is reduced in the absence of pre-hearing efferent modulation. Together, these results demonstrate how afferent and efferent pathways collectively shape spontaneous activity patterns and reveal the important role of efferents in coordinating bilateral spontaneous activity and the emergence of functional responses during the prehearing period. Nature Publishing Group UK 2021-04-27 /pmc/articles/PMC8079389/ /pubmed/33907194 http://dx.doi.org/10.1038/s41467-021-22796-8 Text en © The Author(s) 2021 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Yixiang
Sanghvi, Maya
Gribizis, Alexandra
Zhang, Yueyi
Song, Lei
Morley, Barbara
Barson, Daniel G.
Santos-Sacchi, Joseph
Navaratnam, Dhasakumar
Crair, Michael
Efferent feedback controls bilateral auditory spontaneous activity
title Efferent feedback controls bilateral auditory spontaneous activity
title_full Efferent feedback controls bilateral auditory spontaneous activity
title_fullStr Efferent feedback controls bilateral auditory spontaneous activity
title_full_unstemmed Efferent feedback controls bilateral auditory spontaneous activity
title_short Efferent feedback controls bilateral auditory spontaneous activity
title_sort efferent feedback controls bilateral auditory spontaneous activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079389/
https://www.ncbi.nlm.nih.gov/pubmed/33907194
http://dx.doi.org/10.1038/s41467-021-22796-8
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