钾离子平衡在听力损失中的改变

V. Szűts, J. Jarabin, N. Nagy, F. Otvos, R. Nagy, Attila L Nagy, K. Halasy, L. Rovó, M. Széll, J. Kiss
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引用次数: 3

摘要

连接蛋白、kv型离子通道和泛连接蛋白在维持耳蜗钾离子稳态中起主导作用。细胞背景电流由Kir2.1离子通道维持;然而,它们在听觉系统中的作用尚不清楚。在这项研究中,利用基因定位和免疫荧光方法,从匈牙利白种高加索人群中筛选间隙连接蛋白β 2 (GJB2)、β 3 (GJB3)和β 6 (GJB6)在血液细胞上的翻译蛋白-连接蛋白。研究耳蜗植入前耳聋患者血细胞中连接蛋白和Kir2.1离子通道的表达,结果显示连接蛋白26和连接蛋白43的表达量明显降低。此外,Kir2.1离子通道与突触相关的97蛋白的共表达部分受损。我们的研究发现,耳聋患者的Kir2.1通道水平降低,表明K+通道的功能性Shaker超家族在非病变听力系统中起着至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Altered Potassium Ion Homeostasis in Hearing Loss
Connexins, Kv-type ion channels, and pannexins have a dominant role in maintaining the potassium ion homeostasis in the cochlea. The cellular background currents are sustained by Kir2.1 ion channels; however, their involvement in the hearing system is less clear. In this study, the mutations of gap junction proteins beta 2 (GJB2), beta 3 (GJB3) and beta 6 (GJB6) were screened in the white Caucasian population in Hungary using gene mapping and immunofluorescence methods from translated proteins of these genes—connexins on blood cells. Expression of connexins and Kir2.1 ion channels was investigated in the blood cells of deaf patients prior to cochlear implantation, and the results show significantly decreased amounts of connexin26 and connexin43. In addition, the coexpression of Kir2.1 ion channels with synapse-associated 97 proteins was partially impaired. Our investigation revealed a reduced level of Kir2.1 channels in deaf patients indicating a crucial role for the functional Shaker superfamily of K+ channels in the non-diseased hearing system.
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