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Spatial patterns of noise-induced inner hair cell ribbon loss in the mouse mid-cochlea.


ABSTRACT: In the mammalian cochlea, moderate acoustic overexposure leads to loss of ribbon-type synapse between the inner hair cell (IHC) and its postsynaptic spiral ganglion neuron (SGN), causing a reduced dynamic range of hearing but not a permanent threshold elevation. A prevailing view is that such ribbon loss (known as synaptopathy) selectively impacts the low-spontaneous-rate and high-threshold SGN fibers contacting predominantly the modiolar IHC face. However, the spatial pattern of synaptopathy remains scarcely characterized in the most sensitive mid-cochlear region, where two morphological subtypes of IHC with distinct ribbon size gradients coexist. Here, we used volume electron microscopy to investigate noise exposure-related changes in the mouse IHCs with and without ribbon loss. Our quantifications reveal that IHC subtypes differ in the worst-hit area of synaptopathy. Moreover, we show relative enrichment of mitochondria in the surviving SGN terminals, providing key experimental evidence for the long-proposed role of SGN-terminal mitochondria in synaptic vulnerability.

SUBMITTER: Lu Y 

PROVIDER: S-EPMC10835352 | biostudies-literature | 2024 Feb

REPOSITORIES: biostudies-literature

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Spatial patterns of noise-induced inner hair cell ribbon loss in the mouse mid-cochlea.

Lu Yan Y   Liu Jing J   Li Bei B   Wang Haoyu H   Wang Fangfang F   Wang Shengxiong S   Wu Hao H   Han Hua H   Hua Yunfeng Y  

iScience 20240108 2


In the mammalian cochlea, moderate acoustic overexposure leads to loss of ribbon-type synapse between the inner hair cell (IHC) and its postsynaptic spiral ganglion neuron (SGN), causing a reduced dynamic range of hearing but not a permanent threshold elevation. A prevailing view is that such ribbon loss (known as synaptopathy) selectively impacts the low-spontaneous-rate and high-threshold SGN fibers contacting predominantly the modiolar IHC face. However, the spatial pattern of synaptopathy re  ...[more]

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