平衡的Espin水平对立体纤毛的生长和长度的维持至关重要。

Agnieszka Rzadzinska, Mark Schneider, Konrad Noben-Trauth, James R Bartles, Bechara Kachar
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引用次数: 74

摘要

听力和平衡依赖于感觉毛细胞的微绒毛样肌动蛋白投射,称为立体纤毛。它们在纳米尺度上对机械位移的敏感性需要高度组织的毛发束,其中每个立体纤毛的物理尺寸受到严格控制。每根立体纤毛的长度和直径是在毛束成熟过程中形成的,并通过终身持续的动态调节来维持。在这里,我们通过检测Espin-deficient jerker小鼠(Espn(je))的毛细胞立体纤毛,研究了肌动蛋白捆绑蛋白Espin在立体纤毛生长中的作用,以及短暂过表达Espin对Corti培养器官神经上皮细胞的影响。使用荧光扫描共聚焦和电子显微镜,我们发现Espin的缺乏导致抑制立体纤毛生长,随后是毛束的进行性变性。相反,过度表达Espin诱导立体纤毛和微绒毛的延长,反映了其核心肌动蛋白细丝束的延长。有趣的是,Espin缺乏似乎也影响Myosin XVa的定位,这是一种非常规的肌球蛋白,通常存在于立纤毛尖端,其水平与立纤毛长度成正比。这些结果表明,Espin在内耳神经上皮细胞肌动蛋白基突起的生长和维持中起重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Balanced levels of Espin are critical for stereociliary growth and length maintenance.

Hearing and balance depend on microvilli-like actin-based projections of sensory hair cells called stereocilia. Their sensitivity to mechanical displacements on the nanometer scale requires a highly organized hair bundle in which the physical dimension of each stereocilium is tightly controlled. The length and diameter of each stereocilium are established during hair bundle maturation and maintained by life-long continuing dynamic regulation. Here, we studied the role of the actin-bundling protein Espin in stereociliary growth by examining the hair cell stereocilia of Espin-deficient jerker mice (Espn(je)), and the effects of transiently overexpressing Espin in the neuroepithelial cells of the organ of Corti cultures. Using fluorescence scanning confocal and electron microscopy, we found that a lack of Espin results in inhibition of stereociliary growth followed by progressive degeneration of the hair bundle. In contrast, overexpression of Espin induced lengthening of stereocilia and microvilli that mirrored the elongation of the actin filament bundle at their core. Interestingly, Espin deficiency also appeared to influence the localization of Myosin XVa, an unconventional myosin that is normally present at the stereocilia tip at levels proportional to stereocilia length. These results indicate that Espin is important for the growth and maintenance of the actin-based protrusions of inner ear neuroepithelial cells.

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