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耳蜗毛细胞中踝关节连接复合体的分子特征及其在毛束功能中的作用。

Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning.

作者信息

Michalski Nicolas, Michel Vincent, Bahloul Amel, Lefèvre Gaëlle, Barral Jérémie, Yagi Hideshi, Chardenoux Sébastien, Weil Dominique, Martin Pascal, Hardelin Jean-Pierre, Sato Makoto, Petit Christine

机构信息

Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche en Santé 587, Collège de France, Institut Pasteur, 75724 Paris cedex 15, France.

出版信息

J Neurosci. 2007 Jun 13;27(24):6478-88. doi: 10.1523/JNEUROSCI.0342-07.2007.

Abstract

Several lines of evidence indicate that very large G-protein-coupled receptor 1 (Vlgr1) makes up the ankle links that connect the stereocilia of hair cells at their base. Here, we show that the transmembrane protein usherin, the putative transmembrane protein vezatin, and the PDZ (postsynaptic density-95/Discs large/zona occludens-1) domain-containing submembrane protein whirlin are colocalized with Vlgr1 at the stereocilia base in developing cochlear hair cells and are absent in Vlgr1-/- mice that lack the ankle links. Direct in vitro interactions between these four proteins further support their involvement in a molecular complex associated with the ankle links and scaffolded by whirlin. In addition, the delocalization of these proteins in myosin VIIa defective mutant mice as well as the myosin VIIa tail direct interactions with vezatin, whirlin, and, we show, Vlgr1 and usherin, suggest that myosin VIIa conveys proteins of the ankle-link complex to the stereocilia. Adenylyl cyclase 6, which was found at the base of stereocilia, was both overexpressed and mislocated in Vlgr1-/- mice. In postnatal day 7 Vlgr1-/- mice, mechanoelectrical transduction currents evoked by displacements of the hair bundle toward the tallest stereocilia (i.e., in the excitatory direction) were reduced in outer but not inner hair cells. In both cell types, stimulation of the hair bundle in the opposite direction paradoxically resulted in significant transduction currents. The absence of ankle-link-mediated cohesive forces within hair bundles lacking Vlgr1 may account for the electrophysiological results. However, because some long cadherin-23 isoforms could no longer be detected in Vlgr1-/- mice shortly after birth, the loss of some apical links could be involved too. The premature disappearance of these cadherin isoforms in the Vlgr1-/- mutant argues in favor of a signaling function of the ankle links in hair bundle differentiation.

摘要

多项证据表明,超大G蛋白偶联受体1(Vlgr1)构成了连接毛细胞静纤毛基部的踝关节连接。在此,我们表明跨膜蛋白usherin、假定的跨膜蛋白vezatin以及含PDZ(突触后致密蛋白95/盘状大蛋白/紧密连接蛋白1)结构域的亚膜蛋白whirlin在发育中的耳蜗毛细胞静纤毛基部与Vlgr1共定位,而在缺乏踝关节连接的Vlgr1基因敲除小鼠中则不存在。这四种蛋白之间直接的体外相互作用进一步支持它们参与了与踝关节连接相关且由whirlin搭建的分子复合物。此外,这些蛋白在肌球蛋白VIIa缺陷突变小鼠中的错位,以及肌球蛋白VIIa尾部与vezatin、whirlin的直接相互作用,还有我们所展示的与Vlgr1和usherin的直接相互作用,表明肌球蛋白VIIa将踝关节连接复合物的蛋白转运至静纤毛。在静纤毛基部发现的腺苷酸环化酶6在Vlgr1基因敲除小鼠中既过度表达又定位错误。在出生后第7天的Vlgr1基因敲除小鼠中,毛束向最高静纤毛方向(即兴奋方向)位移所诱发的机械电转导电流在外毛细胞中减少,但在内毛细胞中未减少。在这两种细胞类型中,向相反方向刺激毛束却反常地导致了显著的转导电流。缺乏Vlgr1的毛束内缺乏踝关节连接介导的内聚力可能解释了这些电生理结果。然而,由于出生后不久在Vlgr1基因敲除小鼠中就无法再检测到一些长的钙黏蛋白-23异构体,一些顶端连接的丧失也可能与之有关。Vlgr1基因敲除突变体中这些钙黏蛋白异构体的过早消失支持了踝关节连接在毛束分化中的信号功能。

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