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本文引用的文献

1
Developmental profiling of spiral ganglion neurons reveals insights into auditory circuit assembly.螺旋神经节神经元的发育特征揭示了听觉回路组装的深入见解。
J Neurosci. 2011 Jul 27;31(30):10903-18. doi: 10.1523/JNEUROSCI.2358-11.2011.
2
Canonical Notch signaling is not necessary for prosensory induction in the mouse cochlea: insights from a conditional mutant of RBPjkappa.经典 Notch 信号通路对于小鼠耳蜗前体细胞诱导并非必需:来自 RBPjkappa 条件性突变体的见解。
J Neurosci. 2011 Jun 1;31(22):8046-58. doi: 10.1523/JNEUROSCI.6671-10.2011.
3
Rbpj regulates development of prosensory cells in the mammalian inner ear.Rbpj 调节哺乳动物内耳前体细胞的发育。
Dev Biol. 2011 May 15;353(2):367-79. doi: 10.1016/j.ydbio.2011.03.016. Epub 2011 Mar 21.
4
Conditional deletion of Atoh1 using Pax2-Cre results in viable mice without differentiated cochlear hair cells that have lost most of the organ of Corti.使用 Pax2-Cre 条件性删除 Atoh1 会导致没有分化的耳蜗毛细胞的存活小鼠,这些细胞失去了大部分 Corti 器官。
Hear Res. 2011 May;275(1-2):66-80. doi: 10.1016/j.heares.2010.12.002. Epub 2010 Dec 10.
5
Neurod1 suppresses hair cell differentiation in ear ganglia and regulates hair cell subtype development in the cochlea.Neurod1 抑制耳神经节中的毛细胞分化,并调节耳蜗中毛细胞亚型的发育。
PLoS One. 2010 Jul 22;5(7):e11661. doi: 10.1371/journal.pone.0011661.
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Generation and characterization of Atoh1-Cre knock-in mouse line.Atoh1-Cre基因敲入小鼠品系的构建与鉴定
Genesis. 2010 Jun;48(6):407-13. doi: 10.1002/dvg.20633.
7
Transfection of mouse cochlear explants by electroporation.通过电穿孔法转染小鼠耳蜗外植体。
Curr Protoc Neurosci. 2010 Apr;Chapter 4:Unit 4.34.1-10. doi: 10.1002/0471142301.ns0434s51.
8
Excitatory neurons of the proprioceptive, interoceptive, and arousal hindbrain networks share a developmental requirement for Math1.本体感受、内脏感觉和觉醒后脑网络的兴奋性神经元都需要 Math1 来发育。
Proc Natl Acad Sci U S A. 2009 Dec 29;106(52):22462-7. doi: 10.1073/pnas.0911579106. Epub 2009 Dec 18.
9
A robust and high-throughput Cre reporting and characterization system for the whole mouse brain.一种用于整个小鼠大脑的强大且高通量的 Cre 报告和表征系统。
Nat Neurosci. 2010 Jan;13(1):133-40. doi: 10.1038/nn.2467. Epub 2009 Dec 20.
10
Specification of cell fate in the mammalian cochlea.哺乳动物耳蜗中细胞命运的特化。
Birth Defects Res C Embryo Today. 2009 Sep;87(3):212-21. doi: 10.1002/bdrc.20154.

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.

DOI:10.1016/j.ydbio.2013.01.005
PMID:23318633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3652277/
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。