Conditional Deletion of Atoh1 Reveals Distinct Critical Periods for Survival and Function of Hair Cells in the Organ of Corti

被引:102
作者
Cai, Tiantian [1 ,5 ]
Seymour, Michelle L. [3 ,6 ]
Zhang, Hongyuan [1 ]
Pereira, Fred A. [3 ,4 ,6 ]
Groves, Andrew K. [1 ,2 ,5 ]
机构
[1] Baylor Coll Med, Dept Neurosci, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[4] Baylor Coll Med, Dept Otolaryngol Head & Neck Surg, Houston, TX 77030 USA
[5] Baylor Coll Med, Program Dev Biol, Houston, TX 77030 USA
[6] Baylor Coll Med, Huffington Ctr Aging, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
MATH1; FATE; DIFFERENTIATION; MUTANT; GENE; MECHANISMS; EXPRESSION; GENERATION; MUTATION; NEURONS;
D O I
10.1523/JNEUROSCI.5606-12.2013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:10110 / 10122
页数:13
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