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本文引用的文献

1
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.
2
The first steps towards hearing: mechanisms of otic placode induction.听觉形成的第一步:耳基板诱导机制。
Int J Dev Biol. 2007;51(6-7):463-72. doi: 10.1387/ijdb.072320to.
3
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.
4
Loss of Fgfr3 leads to excess hair cell development in the mouse organ of Corti.成纤维细胞生长因子受体3(Fgfr3)缺失导致小鼠柯蒂氏器中毛细胞过度发育。
Dev Dyn. 2007 Feb;236(2):525-33. doi: 10.1002/dvdy.21026.
5
A morphogenetic wave of p27Kip1 transcription directs cell cycle exit during organ of Corti development.p27Kip1转录的形态发生波在柯蒂氏器发育过程中引导细胞周期退出。
Development. 2006 Aug;133(15):2817-26. doi: 10.1242/dev.02453. Epub 2006 Jun 21.
6
Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family.成纤维细胞生长因子家族的受体特异性。完整的哺乳动物成纤维细胞生长因子家族。
J Biol Chem. 2006 Jun 9;281(23):15694-700. doi: 10.1074/jbc.M601252200. Epub 2006 Apr 4.
7
Expression of Prox1 during mouse cochlear development.Prox1在小鼠耳蜗发育过程中的表达。
J Comp Neurol. 2006 May 10;496(2):172-86. doi: 10.1002/cne.20944.
8
Notch ligands with contrasting functions: Jagged1 and Delta1 in the mouse inner ear.具有相反功能的Notch配体:小鼠内耳中的Jagged1和Delta1
Development. 2006 Apr;133(7):1277-86. doi: 10.1242/dev.02284. Epub 2006 Feb 22.
9
Competence of cranial ectoderm to respond to Fgf signaling suggests a two-step model of otic placode induction.颅外胚层对Fgf信号作出反应的能力提示了耳板诱导的两步模型。
Development. 2006 Mar;133(5):877-87. doi: 10.1242/dev.02267. Epub 2006 Feb 1.
10
The Notch ligand JAG1 is required for sensory progenitor development in the mammalian inner ear.Notch配体JAG1是哺乳动物内耳感觉祖细胞发育所必需的。
PLoS Genet. 2006 Jan;2(1):e4. doi: 10.1371/journal.pgen.0020004. Epub 2006 Jan 13.

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。

Fgf20 is required for sensory epithelial specification in the developing cochlea.

作者信息

Hayashi Toshinori, Ray Catherine A, Bermingham-McDonogh Olivia

机构信息

Virginia Merrill Bloedel Hearing Research Center and Department of Biological Structure, University of Washington, Seattle, Washington 98195, USA.

出版信息

J Neurosci. 2008 Jun 4;28(23):5991-9. doi: 10.1523/JNEUROSCI.1690-08.2008.

DOI:10.1523/JNEUROSCI.1690-08.2008
PMID:18524904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2597653/
Abstract

Tissue-specific deletion of Fgfr1 results in severe defects in the development of both hair cells and support cells (Pirvola et al., 2002). Despite the importance of Fgfr1 in this early phase of cochlear development, the timing for the requirement for FGF signaling at this stage is not known. Therefore, we investigated the requirement for FGF signaling at early stages of cochlear development using an FGF receptor inhibitor. We find that inhibition of FGF signaling from embryonic day 14 (E14) to E16 has a dramatic effect on the development of the sensory epithelium, causing a severe reduction in hair cells and support cells, similar to that reported for the Fgfr1 deletion. The effects of inhibition of FGF signaling on sensory specification are not explained by increases in cell death or changes in proliferation but lead to a rapid reduction in Pea3 and Erm and a loss of Math1 expression. We also show that a specific FGF, FGF20, is the likely ligand for FGFR1 at this sensory specification phase of cochlear development; Fgf20 is expressed at the right time and place to mediate sensory cell specification, and blocking FGF20 with a specific antibody inhibits hair cell and support cell development in a manner similar to the FGF receptor inhibitor. Our results thus define the period of FGF-dependent sensory cell specification and the ligand that mediates this step in cochlear development.

摘要

Fgfr1的组织特异性缺失导致毛细胞和支持细胞发育出现严重缺陷(皮尔沃拉等人,2002年)。尽管Fgfr1在耳蜗发育的这一早期阶段很重要,但在此阶段对FGF信号传导的需求时间尚不清楚。因此,我们使用FGF受体抑制剂研究了耳蜗发育早期对FGF信号传导的需求。我们发现,从胚胎第14天(E14)到E16抑制FGF信号传导对感觉上皮的发育有显著影响,导致毛细胞和支持细胞严重减少,类似于Fgfr1缺失所报道的情况。FGF信号传导抑制对感觉特化的影响不能用细胞死亡增加或增殖变化来解释,而是导致Pea3和Erm迅速减少以及Math1表达丧失。我们还表明,特定的FGF,即FGF20,可能是耳蜗发育这个感觉特化阶段FGFR1的配体;Fgf20在正确的时间和地点表达以介导感觉细胞特化,用特异性抗体阻断FGF20会以类似于FGF受体抑制剂的方式抑制毛细胞和支持细胞的发育。因此,我们的结果确定了FGF依赖的感觉细胞特化时期以及在耳蜗发育中介导这一步骤的配体。