Jung Jinsei, Müller Ulrich
The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Department of Otorhinolaryngology, Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Curr Opin Physiol. 2023 Apr;32. doi: 10.1016/j.cophys.2023.100632. Epub 2023 Jan 25.
Hair cells of the mammalian cochlea are specialized mechanosensory cells that convert mechanical stimuli into electrical signals to initiate the neuronal responses that lead to the perception of sound. The mechanoelectrical transduction (MET) machinery of cochlear hair cells is a multimeric protein complex that consists of the pore forming subunits of the MET channel and several essential accessory subunits that are crucial to regulate channel function and render the channel mechanically sensitive. Mutations have been discovered in the genes that encode all known components of the MET machinery. These mutations cause hearing loss with or without vestibular dysfunction. Some mutations also affect other tissues such as the retina. In this brief review, we will summarize gene mutations that affect the MET machinery of hair cells and how the study of the affected genes has illuminated our understanding of the physiological role of the encoded proteins.
哺乳动物耳蜗的毛细胞是特化的机械感觉细胞,可将机械刺激转化为电信号,从而引发神经元反应,进而产生听觉。耳蜗毛细胞的机械电转导(MET)机制是一种多聚体蛋白复合物,由MET通道的孔形成亚基和几个重要的辅助亚基组成,这些辅助亚基对于调节通道功能和使通道具有机械敏感性至关重要。在编码MET机制所有已知组分的基因中都发现了突变。这些突变会导致伴有或不伴有前庭功能障碍的听力损失。一些突变还会影响其他组织,如视网膜。在这篇简短的综述中,我们将总结影响毛细胞MET机制的基因突变,以及对受影响基因的研究如何阐明了我们对所编码蛋白质生理作用的理解。