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Activated tissue-resident macrophages contribute to hair cell insults in noise-induced hearing loss in mice.
- Source :
-
Communications biology [Commun Biol] 2024 Sep 02; Vol. 7 (1), pp. 1078. Date of Electronic Publication: 2024 Sep 02. - Publication Year :
- 2024
-
Abstract
- Macrophages serve as the primary immune cell population and assume a pivotal role in the immune response within the damaged cochleae. Yet, the origin and role of macrophages in response to noise exposure remain controversial. Here, we take advantage of Ccr2 <superscript>RFP/+</superscript> Cx3cr1 <superscript>GFP/+</superscript> dual-reporter mice to identify the infiltrated and tissue-resident macrophages. After noise exposure, we reveal that activated resident macrophages change in morphology, increase in abundance, and migrate to the region of hair cells, leading to the loss of outer hair cells and the damage of ribbon synapses. Meanwhile, peripheral monocytes are not implicated in the noise-induced hair cell insults. These noise-induced activities of macrophages are abolished by inhibiting TLR4 signaling, resulting in alleviated insults of hair cells and partial recovery of hearing. Our findings indicate cochlear resident macrophages are pro-inflammatory and detrimental players in acoustic trauma and introduce a potential therapeutic target in noise-induced hearing loss.<br /> (© 2024. The Author(s).)
- Subjects :
- Animals
Mice
Mice, Inbred C57BL
Toll-Like Receptor 4 metabolism
Toll-Like Receptor 4 genetics
Hair Cells, Auditory pathology
Hair Cells, Auditory metabolism
Noise adverse effects
Macrophage Activation
Cochlea pathology
Cochlea immunology
Cochlea metabolism
Male
Mice, Transgenic
Hearing Loss, Noise-Induced pathology
Hearing Loss, Noise-Induced immunology
Macrophages immunology
Macrophages metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2399-3642
- Volume :
- 7
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Communications biology
- Publication Type :
- Academic Journal
- Accession number :
- 39223249
- Full Text :
- https://doi.org/10.1038/s42003-024-06768-4