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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.

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。

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