Dendritic Degeneration and Altered Synaptic Innervation of a Central Auditory Neuron During Age-related Hearing Loss

被引:4
|
作者
Wang, Meijian [1 ]
Zhang, Chuangeng [1 ]
Lin, Shengyin [1 ]
Xie, Ruili [1 ,2 ]
机构
[1] Ohio State Univ, Dept Otolaryngol, 400 Tzagournis Med Res Facil ,420 W 12th Ave, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Neurosci, Columbus, OH 43210 USA
关键词
dendritic degeneration; bushy neurons; auditory nerve synapse; cochlear nucleus; age -related hearing loss; calretinin; ANTEROVENTRAL COCHLEAR NUCLEUS; PRIMARY AXOSOMATIC ENDINGS; TEMPORAL FINE-STRUCTURE; HORSERADISH-PEROXIDASE; INHIBITORY INPUTS; SPEECH-PERCEPTION; BUSHY CELLS; RESPONSES; CAT; PRECISION;
D O I
10.1016/j.neuroscience.2023.01.037
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
morphology and synaptic configuration are key determinants of neuronal function and are often modified under pathological conditions. In the first nucleus of the central auditory system, the cochlear nucleus (CN), principal bushy neurons specialize in processing temporal information of sound critical for hearing. These neurons alter their physiological properties during aging that contribute to age-related hearing loss (ARHL). The structural basis of such changes remains unclear, especially age-related modifications in their den-dritic morphology and the innervating auditory nerve (AN) synapses. Using young (2-5 months) and aged (28- 33 months) CBA/CaJ mice of either sex, we filled individual bushy neurons with fluorescent dye in acute brain slices to characterize their dendritic morphology, followed by immunostaining against vesicular glutamate trans-porter 1 (VGluT1) and calretinin (CR) to identify innervating AN synapses. We found that dendritic morphology of aged bushy neurons had significantly reduced complexity, suggesting age-dependent dendritic degeneration, especially in neurons with predominantly non-CR-expressing synapses on the soma. These dendrites were inner-vated by AN bouton synapses, which were predominantly non-CR-expressing in young mice but had increased proportion of CR-expressing synapses in old mice. While somatic AN synapses degenerated substantially with age, as quantified by VGluT1-labeled puncta volume, no significant difference was observed in the total volume of dendritic synapses between young and old mice. Consequently, synaptic density on dendrites was signifi-cantly higher in old mice. The findings suggest that dendritic degeneration and altered synaptic innervation in bushy neurons during aging may underlie their changed physiological activity and contribute to the development of ARHL.(c) 2023 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:25 / 37
页数:13
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