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Spatial patterns of noise-induced inner hair cell ribbon loss in the mouse mid-cochlea.
Lu, Yan; Liu, Jing; Li, Bei; Wang, Haoyu; Wang, Fangfang; Wang, Shengxiong; Wu, Hao; Han, Hua; Hua, Yunfeng.
Afiliação
  • Lu Y; Department of Otolaryngology-Head and Neck Surgery, Shanghai Ninth People's Hospital, Shanghai 200125, China.
  • Liu J; Ear Institute, Shanghai Jiao Tong University School of Medicine, Shanghai 200125, China.
  • Li B; Shanghai Key Laboratory of Translational Medicine on Ear and Nose Diseases, Shanghai 200125, China.
  • Wang H; Shanghai Institute of Precision Medicine, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200125, China.
  • Wang F; Laboratory of Brain Atlas and Brain-inspired Intelligence, Institute of Automation, Chinese Academy of Sciences, Beijing 100190, China.
  • Wang S; Department of Otolaryngology-Head and Neck Surgery, Shanghai Ninth People's Hospital, Shanghai 200125, China.
  • Wu H; Ear Institute, Shanghai Jiao Tong University School of Medicine, Shanghai 200125, China.
  • Han H; Shanghai Key Laboratory of Translational Medicine on Ear and Nose Diseases, Shanghai 200125, China.
  • Hua Y; Shanghai Institute of Precision Medicine, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200125, China.
iScience ; 27(2): 108825, 2024 Feb 16.
Article em En | MEDLINE | ID: mdl-38313060
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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article