Cargando…

Cochlear resident macrophage mediates development of ribbon synapses via CX3CR1/CX3CL1 axis

Cochlear ribbon synapses formed between spiral ganglion neurons and inner hair cells in postnatal mice must undergo significant morphological and functional development to reach auditory maturation. However, the mechanisms underlying cochlear ribbon synapse remodeling remain unclear. This study foun...

Descripción completa

Detalles Bibliográficos
Autores principales: Song, Xinyu, Li, Yang, Guo, Rui, Yu, Qianru, Liu, Shan, Teng, Qi, Chen, Zhong-Rui, Xie, Jing, Gong, Shusheng, Liu, Ke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742371/
https://www.ncbi.nlm.nih.gov/pubmed/36518186
http://dx.doi.org/10.3389/fnmol.2022.1031278
_version_ 1784848500865892352
author Song, Xinyu
Li, Yang
Guo, Rui
Yu, Qianru
Liu, Shan
Teng, Qi
Chen, Zhong-Rui
Xie, Jing
Gong, Shusheng
Liu, Ke
author_facet Song, Xinyu
Li, Yang
Guo, Rui
Yu, Qianru
Liu, Shan
Teng, Qi
Chen, Zhong-Rui
Xie, Jing
Gong, Shusheng
Liu, Ke
author_sort Song, Xinyu
collection PubMed
description Cochlear ribbon synapses formed between spiral ganglion neurons and inner hair cells in postnatal mice must undergo significant morphological and functional development to reach auditory maturation. However, the mechanisms underlying cochlear ribbon synapse remodeling remain unclear. This study found that cochlear resident macrophages are essential for cochlear ribbon synapse development and maturation in mice via the CX3CR1/CX3CL1 axis. CX3CR1 expression (a macrophage surface-specific receptor) and macrophage count in the cochlea were significantly increased from postnatal day 7 then decreased from days 14 to 28. Seven-day treatment with CX3CR1 inhibitors and artificial upregulation of CX3CL1 levels in the inner ear environment using the semicircular canal injection technique were initiated on day 7, and this resulted in a significant increase in hearing threshold on day 28. Additionally, abnormalities in the morphology and number of cochlear ribbon synapses were detected on day P14, which may be associated with hearing impairment. In conclusion, macrophage regulation of cochlear ribbon synapse remodeling via the CX3CR1/CX3CL1 axis is required during hearing development and offers a new perspective on immune-related hearing loss throughout auditory development. Importantly, it could be a new treatment target for sensorineural hearing loss.
format Online
Article
Text
id pubmed-9742371
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-97423712022-12-13 Cochlear resident macrophage mediates development of ribbon synapses via CX3CR1/CX3CL1 axis Song, Xinyu Li, Yang Guo, Rui Yu, Qianru Liu, Shan Teng, Qi Chen, Zhong-Rui Xie, Jing Gong, Shusheng Liu, Ke Front Mol Neurosci Molecular Neuroscience Cochlear ribbon synapses formed between spiral ganglion neurons and inner hair cells in postnatal mice must undergo significant morphological and functional development to reach auditory maturation. However, the mechanisms underlying cochlear ribbon synapse remodeling remain unclear. This study found that cochlear resident macrophages are essential for cochlear ribbon synapse development and maturation in mice via the CX3CR1/CX3CL1 axis. CX3CR1 expression (a macrophage surface-specific receptor) and macrophage count in the cochlea were significantly increased from postnatal day 7 then decreased from days 14 to 28. Seven-day treatment with CX3CR1 inhibitors and artificial upregulation of CX3CL1 levels in the inner ear environment using the semicircular canal injection technique were initiated on day 7, and this resulted in a significant increase in hearing threshold on day 28. Additionally, abnormalities in the morphology and number of cochlear ribbon synapses were detected on day P14, which may be associated with hearing impairment. In conclusion, macrophage regulation of cochlear ribbon synapse remodeling via the CX3CR1/CX3CL1 axis is required during hearing development and offers a new perspective on immune-related hearing loss throughout auditory development. Importantly, it could be a new treatment target for sensorineural hearing loss. Frontiers Media S.A. 2022-11-28 /pmc/articles/PMC9742371/ /pubmed/36518186 http://dx.doi.org/10.3389/fnmol.2022.1031278 Text en Copyright © 2022 Song, Li, Guo, Yu, Liu, Teng, Chen, Xie, Gong and Liu. 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 Molecular Neuroscience
Song, Xinyu
Li, Yang
Guo, Rui
Yu, Qianru
Liu, Shan
Teng, Qi
Chen, Zhong-Rui
Xie, Jing
Gong, Shusheng
Liu, Ke
Cochlear resident macrophage mediates development of ribbon synapses via CX3CR1/CX3CL1 axis
title Cochlear resident macrophage mediates development of ribbon synapses via CX3CR1/CX3CL1 axis
title_full Cochlear resident macrophage mediates development of ribbon synapses via CX3CR1/CX3CL1 axis
title_fullStr Cochlear resident macrophage mediates development of ribbon synapses via CX3CR1/CX3CL1 axis
title_full_unstemmed Cochlear resident macrophage mediates development of ribbon synapses via CX3CR1/CX3CL1 axis
title_short Cochlear resident macrophage mediates development of ribbon synapses via CX3CR1/CX3CL1 axis
title_sort cochlear resident macrophage mediates development of ribbon synapses via cx3cr1/cx3cl1 axis
topic Molecular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742371/
https://www.ncbi.nlm.nih.gov/pubmed/36518186
http://dx.doi.org/10.3389/fnmol.2022.1031278
work_keys_str_mv AT songxinyu cochlearresidentmacrophagemediatesdevelopmentofribbonsynapsesviacx3cr1cx3cl1axis
AT liyang cochlearresidentmacrophagemediatesdevelopmentofribbonsynapsesviacx3cr1cx3cl1axis
AT guorui cochlearresidentmacrophagemediatesdevelopmentofribbonsynapsesviacx3cr1cx3cl1axis
AT yuqianru cochlearresidentmacrophagemediatesdevelopmentofribbonsynapsesviacx3cr1cx3cl1axis
AT liushan cochlearresidentmacrophagemediatesdevelopmentofribbonsynapsesviacx3cr1cx3cl1axis
AT tengqi cochlearresidentmacrophagemediatesdevelopmentofribbonsynapsesviacx3cr1cx3cl1axis
AT chenzhongrui cochlearresidentmacrophagemediatesdevelopmentofribbonsynapsesviacx3cr1cx3cl1axis
AT xiejing cochlearresidentmacrophagemediatesdevelopmentofribbonsynapsesviacx3cr1cx3cl1axis
AT gongshusheng cochlearresidentmacrophagemediatesdevelopmentofribbonsynapsesviacx3cr1cx3cl1axis
AT liuke cochlearresidentmacrophagemediatesdevelopmentofribbonsynapsesviacx3cr1cx3cl1axis