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缺乏功能性肌球蛋白XV a时的听觉机械转导

Auditory mechanotransduction in the absence of functional myosin-XVa.

作者信息

Stepanyan Ruben, Belyantseva Inna A, Griffith Andrew J, Friedman Thomas B, Frolenkov Gregory I

机构信息

Department of Physiology, University of Kentucky, MS508, Chandler Medical Center, 800 Rose Street, Lexington, KY 40536, USA.

出版信息

J Physiol. 2006 Nov 1;576(Pt 3):801-8. doi: 10.1113/jphysiol.2006.118547. Epub 2006 Sep 14.

Abstract

In hair cells of all vertebrates, a mechanosensory bundle is formed by stereocilia with precisely graded heights. Unconventional myosin-XVa is critical for formation of this bundle because it transports whirlin and perhaps other molecular components responsible for programmed elongation of stereocilia to the stereocilia tips. A tip of a stereocilium is the site of stereocilia growth and one of the proposed sites of mechano-electrical transduction. In adult shaker 2 mice, a mutation that disables the motor function of myosin-XVa results in profound deafness and abnormally short stereocilia that lack stereocilia links, an indispensable component of mechanotransduction machinery. Therefore, it was assumed that myosin-XVa is required for proper formation of the mechanotransduction apparatus. Here we show that in young postnatal shaker 2 mice, abnormally short stereocilia bundles of auditory hair cells have numerous stereocilia links and 'wild type' mechano-electrical transduction. We compared the mechanotransduction current in auditory hair cells of young normal-hearing littermates, myosin-XVa-deficient shaker 2 mice, and whirler mice that have similarly short stereocilia but intact myosin-XVa at the stereocilia tips. This comparison revealed that the absence of functional myosin-XVa does not disrupt adaptation of the mechanotransduction current during sustained bundle deflection. Thus, the hair cell mechanotransduction complex forms and functions independently from myosin-XVa-based hair bundle morphogenesis.

摘要

在所有脊椎动物的毛细胞中,机械感觉束由高度精确分级的静纤毛形成。非传统肌球蛋白-XVa对该束的形成至关重要,因为它将whirlin以及可能其他负责静纤毛程序性伸长的分子成分运输到静纤毛尖端。静纤毛的尖端是静纤毛生长的部位,也是机械电转导的假定部位之一。在成年的shaker 2小鼠中,一种使肌球蛋白-XVa的运动功能丧失的突变导致严重耳聋和静纤毛异常短小,且缺乏机械转导机制不可或缺的组成部分——静纤毛连接。因此,人们认为肌球蛋白-XVa是机械转导装置正常形成所必需的。在此我们表明,在出生后早期的shaker 2小鼠中,听觉毛细胞异常短小的静纤毛束有许多静纤毛连接和“野生型”机械电转导。我们比较了正常听力的同窝幼崽、缺乏肌球蛋白-XVa的shaker 2小鼠以及静纤毛同样短小但静纤毛尖端肌球蛋白-XVa完整的whirler小鼠的听觉毛细胞中的机械转导电流。这种比较表明,功能性肌球蛋白-XVa的缺失在静纤毛束持续偏转期间不会破坏机械转导电流的适应性。因此,毛细胞机械转导复合体的形成和功能独立于基于肌球蛋白-XVa的毛束形态发生。

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