首页> 美国卫生研究院文献>PLoS Genetics >Roles of the Espin Actin-Bundling Proteins in the Morphogenesis and Stabilization of Hair Cell Stereocilia Revealed in CBA/CaJ Congenic Jerker Mice
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Roles of the Espin Actin-Bundling Proteins in the Morphogenesis and Stabilization of Hair Cell Stereocilia Revealed in CBA/CaJ Congenic Jerker Mice

机译:Espin肌动蛋白捆绑蛋白的作用在CBA / CaJ同基因抽搐小鼠中揭示的毛细胞胞浆菌的形态发生和稳定性中的作用

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摘要

Hearing and vestibular function depend on mechanosensory staircase collections of hair cell stereocilia, which are produced from microvillus-like precursors as their parallel actin bundle scaffolds increase in diameter and elongate or shorten. Hair cell stereocilia contain multiple classes of actin-bundling protein, but little is known about what each class contributes. To investigate the roles of the espin class of actin-bundling protein, we used a genetic approach that benefited from a judicious selection of mouse background strain and an examination of the effects of heterozygosity. A congenic jerker mouse line was prepared by repeated backcrossing into the inbred CBA/CaJ strain, which is known for excellent hearing and minimal age-related hearing loss. We compared stereocilia in wild-type CBA/CaJ mice, jerker homozygotes that lack espin proteins owing to a frameshift mutation in the espin gene, and jerker heterozygotes that contain reduced espin levels. The lack of espins radically impaired stereociliary morphogenesis, resulting in stereocilia that were abnormally thin and short, with reduced differential elongation to form a staircase. Mean stereociliary diameter did not increase beyond ∼0.10–0.14 µm, making stereocilia ∼30%–60% thinner than wild type and suggesting that they contained ∼50%–85% fewer actin filaments. These characteristics indicate a requirement for espins in the appositional growth and differential elongation of the stereociliary parallel actin bundle and fit the known biological activities of espins in vitro and in transfected cells. The stereocilia of jerker heterozygotes showed a transient proximal-distal tapering suggestive of haploinsufficiency and a slowing of morphogenesis that revealed previously unrecognized assembly steps and intermediates. The lack of espins also led to a region-dependent degeneration of stereocilia involving shortening and collapse. We conclude that the espin actin-bundling proteins are required for the assembly and stabilization of the stereociliary parallel actin bundle.
机译:听力和前庭功能取决于毛细胞立体纤毛的机械感官楼梯集合,这些集合是由微绒毛状前体产生的,因为它们的平行肌动蛋白束支架直径增大,伸长或缩短。毛细胞立体纤毛包含多种类型的肌动蛋白束蛋白,但对于每种类型的贡献却鲜为人知。为了研究espin类肌动蛋白捆绑蛋白的作用,我们使用了一种遗传方法,该方法得益于对小鼠背景菌株的明智选择以及对杂合性的影响的检查。通过重复回交近交CBA / CaJ品系来制备同系抽搐小鼠品系,该品系以出色的听力和与年龄相关的最小听力损失而著称。我们比较了野生型CBA / CaJ小鼠中的立体纤毛,由于espin基因的移码突变而缺乏espin蛋白的抽搐纯合子和包含降低的espin水平的抽搐杂合子。缺乏旋风从根本上削弱了立体睫毛的形态发生,导致立体睫毛异常稀疏和短小,差异伸长率降低,从而形成了阶梯。平均纤毛纤丝直径没有增加到超过〜0.10–0.14 µm,使纤毛纤毛比野生型纤毛纤细约30%–60%,这表明它们的肌动蛋白丝减少了约50%–85%。这些特征表明espins在立体睫状平行肌动蛋白束的并置生长和差异伸长中的需求,并适合espins在体外和转染细胞中的已知生物学活性。抽搐杂合子的立体纤毛显示出短暂的近端至远端逐渐变细,提示单倍体功能不全和形态发生减慢,这揭示了以前无法识别的组装步骤和中间体。缺乏旋风也导致视锥细胞的区域依赖性变性,包括缩短和塌陷。我们得出结论,espin肌动蛋白捆绑蛋白是立体睫状平行肌动蛋白束的组装和稳定所必需的。

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