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条件性敲除 Atoh1 揭示了耳蜗毛细胞存活和功能的不同关键期。

Conditional deletion of Atoh1 reveals distinct critical periods for survival and function of hair cells in the organ of Corti.

机构信息

Department of Neuroscience, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

J Neurosci. 2013 Jun 12;33(24):10110-22. doi: 10.1523/JNEUROSCI.5606-12.2013.

Abstract

Atonal homolog1 (Atoh1) encodes a basic helix-loop-helix protein that is the first transcription factor to be expressed in differentiating hair cells. Previous work suggests that expression of Atoh1 in prosensory precursors is necessary for the differentiation and survival of hair cells, but it is not clear whether Atoh1 is required exclusively for these processes, or whether it regulates other functions later during hair cell maturation. We used EGFP-tagged Atoh1 knock-in mice to demonstrate for the first time that Atoh1 protein is expressed in hair cell precursors several days before the appearance of differentiated markers, but not in the broad pattern expected of a proneural gene. We conditionally deleted Atoh1 at different points in hair cell development and observe a rapid onset of hair cell defects, suggesting that the Atoh1 protein is unstable in differentiating hair cells and is necessary through an extended phase of their differentiation. Conditional deletion of Atoh1 reveals multiple functions in hair cell survival, maturation of stereociliary bundles, and auditory function. We show the presence of distinct critical periods for Atoh1 in each of these functions, suggesting that Atoh1 may be directly regulating many aspects of hair cell function. Finally, we show that the supporting cell death that accompanies loss of Atoh1 in hair cells is likely caused by the abortive trans-differentiation of supporting cells into hair cells. Together our data suggest that Atoh1 regulates multiple aspects of hair cell development and function.

摘要

Atonal homolog1(Atoh1)编码一种碱性螺旋-环-螺旋蛋白,是第一个在分化的毛细胞中表达的转录因子。先前的工作表明,前感觉前体中 Atoh1 的表达对于毛细胞的分化和存活是必要的,但尚不清楚 Atoh1 是否专门用于这些过程,或者它是否在毛细胞成熟的后期调节其他功能。我们使用 EGFP 标记的 Atoh1 敲入小鼠首次证明,Atoh1 蛋白在出现分化标志物的前几天就在毛细胞前体中表达,但不在预期的神经前基因的广泛模式中。我们在毛细胞发育的不同时间点条件性地删除了 Atoh1,并观察到毛细胞缺陷的快速出现,这表明 Atoh1 蛋白在分化的毛细胞中不稳定,并且在其分化的延长阶段是必需的。Atoh1 的条件性缺失揭示了 Atoh1 在毛细胞存活、静纤毛束成熟和听觉功能中的多种功能。我们表明,Atoh1 在这些功能中的每一个都存在不同的关键时期,这表明 Atoh1 可能直接调节毛细胞功能的许多方面。最后,我们表明,伴随 Atoh1 在毛细胞中缺失的支持细胞死亡可能是由支持细胞向毛细胞的失败转分化引起的。我们的数据表明,Atoh1 调节毛细胞发育和功能的多个方面。

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