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Building the world's best hearing aid; regulation of cell fate in the cochlea.打造世界上最好的助听器;耳蜗中细胞命运的调控。
Curr Opin Genet Dev. 2009 Aug;19(4):368-73. doi: 10.1016/j.gde.2009.06.004. Epub 2009 Jul 13.
2
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Hey1 and Hey2 control the spatial and temporal pattern of mammalian auditory hair cell differentiation downstream of Hedgehog signaling.Hey1 和 Hey2 控制 Hedgehog 信号下游哺乳动物听觉毛细胞分化的时空模式。
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Correct timing of proliferation and differentiation is necessary for normal inner ear development and auditory hair cell viability.正确的增殖和分化时间对于正常内耳发育和听觉毛细胞活力是必要的。
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本文引用的文献

1
Sox2 signaling in prosensory domain specification and subsequent hair cell differentiation in the developing cochlea.Sox2信号在发育中的耳蜗感觉前体细胞区域特化及随后的毛细胞分化过程中的作用
Proc Natl Acad Sci U S A. 2008 Nov 25;105(47):18396-401. doi: 10.1073/pnas.0808175105. Epub 2008 Nov 14.
2
Functional auditory hair cells produced in the mammalian cochlea by in utero gene transfer.通过子宫内基因转移在哺乳动物耳蜗中产生的功能性听觉毛细胞。
Nature. 2008 Sep 25;455(7212):537-41. doi: 10.1038/nature07265. Epub 2008 Aug 27.
3
Eya1 gene dosage critically affects the development of sensory epithelia in the mammalian inner ear.Eya1基因剂量严重影响哺乳动物内耳感觉上皮的发育。
Hum Mol Genet. 2008 Nov 1;17(21):3340-56. doi: 10.1093/hmg/ddn229. Epub 2008 Aug 4.
4
Hedgehog signaling regulates sensory cell formation and auditory function in mice and humans.刺猬信号通路调节小鼠和人类的感觉细胞形成及听觉功能。
J Neurosci. 2008 Jul 16;28(29):7350-8. doi: 10.1523/JNEUROSCI.0312-08.2008.
5
Jxc1/Sobp, encoding a nuclear zinc finger protein, is critical for cochlear growth, cell fate, and patterning of the organ of corti.编码一种核锌指蛋白的Jxc1/Sobp对耳蜗生长、细胞命运及柯蒂氏器的模式形成至关重要。
J Neurosci. 2008 Jun 25;28(26):6633-41. doi: 10.1523/JNEUROSCI.1280-08.2008.
6
Fgf20 is required for sensory epithelial specification in the developing cochlea.成纤维细胞生长因子20(Fgf20)是发育中的耳蜗感觉上皮特化所必需的。
J Neurosci. 2008 Jun 4;28(23):5991-9. doi: 10.1523/JNEUROSCI.1690-08.2008.
7
Bmp4 is essential for the formation of the vestibular apparatus that detects angular head movements.骨形态发生蛋白4(Bmp4)对于检测头部角向运动的前庭器官的形成至关重要。
PLoS Genet. 2008 Apr 11;4(4):e1000050. doi: 10.1371/journal.pgen.1000050.
8
Hesr1 and Hesr2 may act as early effectors of Notch signaling in the developing cochlea.Hesr1和Hesr2可能作为发育中的耳蜗中Notch信号通路的早期效应分子发挥作用。
Dev Biol. 2008 Apr 1;316(1):87-99. doi: 10.1016/j.ydbio.2008.01.006. Epub 2008 Jan 18.
9
Fgf8 induces pillar cell fate and regulates cellular patterning in the mammalian cochlea.成纤维细胞生长因子8(Fgf8)诱导柱状细胞命运并调节哺乳动物耳蜗中的细胞模式。
Development. 2007 Aug;134(16):3021-9. doi: 10.1242/dev.02874. Epub 2007 Jul 18.
10
Expression of LHX3 and SOX2 during mouse inner ear development.LHX3和SOX2在小鼠内耳发育过程中的表达。
Gene Expr Patterns. 2007 Aug;7(7):798-807. doi: 10.1016/j.modgep.2007.05.002. Epub 2007 May 26.

打造世界上最好的助听器;耳蜗中细胞命运的调控。

Building the world's best hearing aid; regulation of cell fate in the cochlea.

作者信息

Puligilla Chandrakala, Kelley Matthew W

机构信息

Section on Developmental Neuroscience, National Institute on Deafness and other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Curr Opin Genet Dev. 2009 Aug;19(4):368-73. doi: 10.1016/j.gde.2009.06.004. Epub 2009 Jul 13.

DOI:10.1016/j.gde.2009.06.004
PMID:19604683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2845966/
Abstract

In mammals, auditory perception is initially mediated through sensory cells located in a rigorously patterned mosaic of unique cell types located within the coiled cochlea. Identification of the factors that direct multipotent progenitor cells to develop as each of these specialized cell types has the potential to enhance our understanding of the development of the auditory system and to identify potential targets for regenerative therapies. Recent results have identified specific signaling molecules and pathways, including Notch, Hedgehog, Sox2 and Fgfs, that guide progenitor cells to develop first as a sensory precursor, referred to as a prosensory cell, and subsequently as one of the specialized cell types within the sensory mosaic.

摘要

在哺乳动物中,听觉感知最初是通过位于卷曲耳蜗内由独特细胞类型构成的严格模式化镶嵌结构中的感觉细胞来介导的。确定引导多能祖细胞发育成这些特殊细胞类型中每一种的因素,有可能增进我们对听觉系统发育的理解,并确定再生疗法的潜在靶点。最近的研究结果已经确定了特定的信号分子和信号通路,包括Notch、Hedgehog、Sox2和Fgf,这些信号分子和信号通路引导祖细胞首先发育成一种感觉前体细胞,即前感觉细胞,随后发育成感觉镶嵌结构中的一种特殊细胞类型。