Department of Otolaryngology, Kresge Hearing Research Institute, Ann Arbor, MI, USA.
Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI, USA.
J Physiol. 2022 Jan;600(1):61-73. doi: 10.1113/JP282262. Epub 2021 Dec 6.
Understanding communication signals, especially in noisy environments, is crucial to social interactions. Yet, as we age, acoustic signals can be disrupted by cochlear damage and the subsequent auditory nerve fibre degeneration. The most vulnerable medium- and high-threshold-auditory nerve fibres innervate various cell types in the cochlear nucleus, among which the small cells are unique in receiving this input exclusively. Furthermore, small cells project to medial olivocochlear (MOC) neurons, which in turn send branched collaterals back into the small cell cap. Here, we use single-unit recordings to characterise small cell firing characteristics and demonstrate superior intensity coding in this cell class. We show converse effects when activating/blocking the MOC system, demonstrating that small-cell unique coding properties are facilitated by direct cholinergic input from the MOC system. Small cells also maintain tone-level coding in the presence of background noise. Finally, small cells precisely code low-frequency modulation more accurately than other ventral cochlear nucleus cell types, demonstrating accurate envelope coding that may be important for vocalisation processing. These results highlight the small cell olivocochlear circuit as a key player in signal processing in noisy environments, which may be selectively degraded in ageing or after noise insult. KEY POINTS: Cochlear nucleus small cells receive input from low/medium spontaneous rate auditory nerve fibres and medial olivocochlear neurons. Electrical stimulation of medial olivocochlear neurons in the ventral nucleus of the trapezoid body and blocking cholinergic input to small cells using atropine demonstrates an excitatory cholinergic input to small cells, which increases responses to suprathreshold sound. Unique inputs to small cells produce superior sound intensity coding. This coding of intensity is preserved in the presence of background noise, an effect exclusive to this cell type in the cochlear nucleus. These results suggest that small cells serve an essential function in the ascending auditory system, which may be relevant to disorders such as hidden hearing loss.
理解通讯信号,尤其是在嘈杂环境中,对社交互动至关重要。然而,随着年龄的增长,耳蜗损伤和随后的听神经纤维变性会干扰声信号。中等和高阈值听觉神经纤维最易受损,它们支配耳蜗核中的各种细胞类型,其中小细胞的独特之处在于其仅接收这种输入。此外,小细胞投射到内侧橄榄耳蜗(MOC)神经元,后者反过来又将分支侧支返回到小细胞帽。在这里,我们使用单细胞记录来描述小细胞的放电特征,并证明该细胞类别的强度编码具有优越性。当激活/阻断 MOC 系统时,我们会显示出相反的效果,这表明小细胞独特的编码特性是由 MOC 系统的直接胆碱能输入促进的。小细胞在存在背景噪声的情况下也能保持音高编码。最后,小细胞比其他耳蜗腹核细胞类型更准确地编码低频调制,证明了对声音处理很重要的精确包络编码。这些结果强调了小细胞橄榄耳蜗回路作为嘈杂环境中信号处理的关键参与者,其可能在衰老或噪声损伤后选择性退化。关键点:耳蜗核小细胞接收来自低/中自发率听觉神经纤维和内侧橄榄耳蜗神经元的输入。电刺激梯形体腹侧核中的内侧橄榄耳蜗神经元并用阿托品阻断小细胞的胆碱能输入,证明了小细胞的兴奋性胆碱能输入增加了对阈上声音的反应。小细胞的独特输入产生了优越的声音强度编码。这种强度编码在存在背景噪声的情况下得以保留,这是耳蜗核中该细胞类型独有的效应。这些结果表明,小细胞在听觉上行系统中起着至关重要的作用,这可能与隐藏性听力损失等疾病有关。