Liang Chun, Zhai Tian-Ying, Fang Shu, Chen Jin, Liu Li-Man, Yu Ning, Zhao Hong-Bo
bioRxiv. 2024 Oct 16:2024.10.14.618333. doi: 10.1101/2024.10.14.618333.
Hearing sensitivity and noise protection are mediated and determined by negative feedback of the cochlear efferent system. Type II auditory nerves (ANs) innervate outer hair cells (OHCs) in the cochlea and provide an input to this efferent control. However, little is known about underlying channel information. Here, we report that ATP-gated P2x7 receptor had a predominant expression at type II ANs and the synaptic areas under inner hair cells and OHCs with lateral and medial olivocochlear efferent nerves. Knockout (KO) of P2x7 increased hearing sensitivity with enhanced acoustic startle response (ASR), auditory brainstem response (ABR), and cochlear microphonics (CM) by increasing OHC electromotility, an active cochlear amplifier in mammals. P2x7 KO also increased susceptibility to noise. Middle level noise exposure could impair active cochlear mechanics resulting in permanent hearing loss in P2x7 KO mice. These data demonstrate that P2x7 receptors have a critical role in type II AN function and the cochlear efferent system to control hearing sensitivity; deficiency of P2x7 receptors can impair the cochlear efferent suppression leading to hearing oversensitivity and susceptibility to noise.
听觉敏感性和噪声保护由耳蜗传出系统的负反馈介导和决定。II型听觉神经(ANs)支配耳蜗中的外毛细胞(OHCs),并为这种传出控制提供输入。然而,关于潜在的通道信息知之甚少。在这里,我们报告ATP门控的P2x7受体在II型ANs以及内毛细胞和OHCs下方与外侧和内侧橄榄耳蜗传出神经的突触区域有主要表达。P2x7基因敲除(KO)通过增加OHC电运动性(哺乳动物中的一种主动耳蜗放大器)提高了听觉敏感性,增强了听觉惊吓反应(ASR)、听觉脑干反应(ABR)和耳蜗微音电位(CM)。P2x7基因敲除还增加了对噪声的易感性。中等强度的噪声暴露会损害主动耳蜗力学,导致P2x7基因敲除小鼠永久性听力损失。这些数据表明,P2x7受体在II型AN功能和耳蜗传出系统中对控制听觉敏感性起关键作用;P2x7受体的缺乏会损害耳蜗传出抑制,导致听觉超敏和对噪声的易感性。