Kindt Katie S, Sheets Lavinia
Section on Sensory Cell Development and Function, NIDCD/National Institutes of Health, Bethesda, MD, United States.
Department of Otolaryngology, Washington University School of Medicine, St. Louis, MO, United States.
Front Cell Dev Biol. 2018 Sep 11;6:114. doi: 10.3389/fcell.2018.00114. eCollection 2018.
Sensorineural hearing loss is the most common form of hearing loss in humans, and results from either dysfunction in hair cells, the sensory receptors of sound, or the neurons that innervate hair cells. A specific type of sensorineural hearing loss, referred to as auditory synaptopathy, occurs when hair cells are able to detect sound but fail to transmit sound stimuli at the hair-cell synapse. Auditory synaptopathy can originate from genetic alterations that specifically disrupt hair-cell synapse function. Additionally, environmental factors such as noise exposure can leave hair cells intact but result in loss of hair-cell synapses, and represent an acquired form of auditory synaptopathy. The zebrafish model has emerged as a valuable system for studies of hair-cell function, and specifically hair-cell synaptopathy. In this review, we describe the experimental tools that have been developed to study hair-cell synapses in zebrafish. We discuss how zebrafish genetics has helped identify and define the roles of hair-cell synaptic proteins crucial for hearing in humans, and highlight how studies in zebrafish have contributed to our understanding of hair-cell synapse formation and function. In addition, we also discuss work that has used noise exposure or pharmacological mimic of noise-induced excitotoxicity in zebrafish to define cellular mechanisms underlying noise-induced hair-cell damage and synapse loss. Lastly, we highlight how future studies in zebrafish could enhance our understanding of the pathological processes underlying synapse loss in both genetic and acquired auditory synaptopathy. This knowledge is critical in order to develop therapies that protect or repair auditory synaptic contacts.
感音神经性听力损失是人类最常见的听力损失形式,其起因是毛细胞(声音的感觉感受器)或支配毛细胞的神经元功能失调。一种特定类型的感音神经性听力损失,称为听觉突触病,当毛细胞能够检测声音但无法在毛细胞突触处传递声音刺激时就会发生。听觉突触病可能源于特异性破坏毛细胞突触功能的基因改变。此外,诸如噪声暴露等环境因素可使毛细胞保持完整,但会导致毛细胞突触丧失,这代表了一种后天获得性的听觉突触病。斑马鱼模型已成为研究毛细胞功能,特别是毛细胞突触病的重要系统。在这篇综述中,我们描述了已开发出的用于研究斑马鱼毛细胞突触的实验工具。我们讨论了斑马鱼遗传学如何帮助识别和定义对人类听力至关重要的毛细胞突触蛋白的作用,并强调了斑马鱼研究如何有助于我们理解毛细胞突触的形成和功能。此外,我们还讨论了利用噪声暴露或药物模拟噪声诱导的兴奋性毒性在斑马鱼中进行的研究,以确定噪声诱导的毛细胞损伤和突触丧失的细胞机制。最后,我们强调了未来在斑马鱼中的研究如何能够增进我们对遗传性和后天获得性感音神经性听力损失中突触丧失的病理过程的理解。这些知识对于开发保护或修复听觉突触连接的疗法至关重要。