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The Rho GTPase Cdc42 regulates hair cell planar polarity and cellular patterning in the developing cochlea

机译:Rho GTPase Cdc42调节发育中的耳蜗中的毛细胞平面极性和细胞模式

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摘要

Hair cells of the organ of Corti (OC) of the cochlea exhibit distinct planar polarity, both at the tissue and cellular level. Planar polarity at tissue level is manifested as uniform orientation of the hair cell stereociliary bundles. Hair cell intrinsic polarity is defined as structural hair bundle asymmetry; positioning of the kinocilium/basal body complex at the vertex of the V-shaped bundle. Consistent with strong apical polarity, the hair cell apex displays prominent actin and microtubule cytoskeletons. The Rho GTPase Cdc42 regulates cytoskeletal dynamics and polarization of various cell types, and, thus, serves as a candidate regulator of hair cell polarity. We have here induced Cdc42 inactivation in the late-embryonic OC. We show the role of Cdc42 in the establishment of planar polarity of hair cells and in cellular patterning. Abnormal planar polarity was displayed as disturbances in hair bundle orientation and morphology and in kinocilium/basal body positioning. These defects were accompanied by a disorganized cell-surface microtubule network. Atypical protein kinase C (aPKC), a putative Cdc42 effector, colocalized with Cdc42 at the hair cell apex, and aPKC expression was altered upon Cdc42 depletion. Our data suggest that Cdc42 together with aPKC is part of the machinery establishing hair cell planar polarity and that Cdc42 acts on polarity through the cell-surface microtubule network. The data also suggest that defects in apical polarization are influenced by disturbed cellular patterning in the OC. In addition, our data demonstrates that Cdc42 is required for stereociliogenesis in the immature cochlea.
机译:耳蜗的Corti(OC)器官的毛细胞在组织和细胞水平上均表现出独特的平面极性。组织水平的平面极性表现为毛细胞立体纤毛束的均匀方向。毛细胞固有极性定义为结构性发束不对称;在K形束的顶点处定位运动蛋白/基体复合物。与强烈的顶端极性一致,毛细胞顶点显示出突出的肌动蛋白和微管细胞骨架。 Rho GTPase Cdc42调节各种细胞类型的细胞骨架动力学和极化,因此可作为毛细胞极性的候选调节剂。我们在这里已在胚胎后期OC中诱导了Cdc42失活。我们显示Cdc42在毛细胞平面极性的建立和细胞模式中的作用。异常的平面极性显示为束发方向和形态以及运动蛋白/基体位置的干扰。这些缺陷伴有杂乱无章的细胞表面微管网络。非典型蛋白激酶C(aPKC),一种假定的Cdc42效应子,与Cdc42在毛细胞顶点共定位,并且在Cdc42耗尽时aPKC表达发生改变。我们的数据表明Cdc42和aPKC是建立毛细胞平面极性的机制的一部分,并且Cdc42通过细胞表面微管网络作用于极性。数据还表明,根尖极化的缺陷受OC中细胞图谱的干扰。此外,我们的数据表明Cdc42是未成熟的耳蜗中立体睫毛发生所必需的。

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