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Atoh1 谱系在哺乳动物耳蜗中产生毛细胞和支持细胞。

The Atoh1-lineage gives rise to hair cells and supporting cells within the mammalian cochlea.

机构信息

Laboratory of Cochlear Development, National Institute on Deafness and Other Communications Disorders, NIH, Bethesda, MD 20892, USA.

出版信息

Dev Biol. 2013 Apr 1;376(1):86-98. doi: 10.1016/j.ydbio.2013.01.005. Epub 2013 Jan 11.

Abstract

The organ of Corti, located within the mammalian cochlea, contains a precise mosaic of hair cells (HC) and supporting cells (SC), the patterning of which is critical for auditory function. Progenitors of HCs and SCs are found in the same post-mitotic region of the cochlear duct during early stages of cochlear development, and both HCs and SCs are absent in mice lacking the transcription factor Atoh1. Based on existing data, Atoh1 is thought to be the earliest determinant of HC fate, and to have a cell-autonomous role in HC differentiation, but the lineage of Atoh1-positive cells within the cochlear duct remains unclear. To address this issue, we used an inducible Atoh1(Cre⁎PR) allele to permanently mark Atoh1-expressing cells at different developmental time points. We found that up to 30% of cells from the Atoh1-lineage develop as SCs, and that the number of Atoh1-positive SCs decreases both spatially and temporally in a pattern consistent with ongoing commitment. Modulation of Notch signaling, necessary for formation of the HC-SC mosaic, changes the percentage of cells from the Atoh1-lineage that develop as either HCs or SCs. The HC-SC ratio is also affected by morphogenesis of the cochlea, as inhibiting the outgrowth of the cochlear duct increases the number of Atoh1-lineage cells that develop as SCs. Our results demonstrate that the Atoh1-lineage is established early in cochlear development, but also show that expression of Atoh1 does not absolutely result in commitment to a HC fate.

摘要

科蒂器位于哺乳动物耳蜗内,包含精确的毛细胞(HC)和支持细胞(SC)镶嵌模式,其模式对于听觉功能至关重要。在耳蜗发育的早期阶段,HC 和 SC 的祖细胞存在于耳蜗管的同一个有丝分裂后区域,并且在缺乏转录因子 Atoh1 的小鼠中,HC 和 SC 均不存在。根据现有数据,Atoh1 被认为是 HC 命运的最早决定因素,并且在 HC 分化中具有细胞自主作用,但耳蜗管内 Atoh1 阳性细胞的谱系仍然不清楚。为了解决这个问题,我们使用可诱导的 Atoh1(Cre⁎PR)等位基因在不同的发育时间点永久标记 Atoh1 表达细胞。我们发现,多达 30%的 Atoh1 谱系细胞分化为 SC,并且 Atoh1 阳性 SC 的数量在空间和时间上都减少,这与持续的分化一致。 Notch 信号的调节,对于 HC-SC 镶嵌的形成是必需的,改变了 Atoh1 谱系细胞分化为 HC 或 SC 的百分比。HC-SC 比例也受到耳蜗形态发生的影响,因为抑制耳蜗管的生长会增加 Atoh1 谱系细胞分化为 SC 的数量。我们的结果表明,Atoh1 谱系在耳蜗发育的早期就已经建立,但也表明 Atoh1 的表达并不绝对导致 HC 命运的确定。

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