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发育中的下颌骨内内皮素-A受体基因的缺失。

Deletion of the endothelin-A receptor gene within the developing mandible.

作者信息

Ruest Louis-Bruno, Kedzierski Rafal, Yanagisawa Masashi, Clouthier David E

机构信息

Department of Molecular, Cellular and Craniofacial Biology and the Birth Defects Center, University of Louisville, Louisville, KY, 40292, USA.

出版信息

Cell Tissue Res. 2005 Mar;319(3):447-53. doi: 10.1007/s00441-004-0988-1. Epub 2005 Jan 13.

Abstract

Signaling from the endothelin-A (Ednra) receptor is responsible for initiating multiple signaling pathways within neural crest cells (NCCs). Loss of this initiation is presumably the basis for the craniofacial defects observed in Ednra-/- embryos. However, it is not known whether continued Ednra signaling in NCC derivatives is required for subsequent development of the lower jaw. To address this question, mice containing loxP recombination sequences flanking a portion of the Ednra gene were bred with transgenic mice that express Cre recombinase under control of a Dlx5/6 enhancer element. We find that while Ednra gene inactivation within the mandibular arch of these Ednra conditional knockout embryos is detectable by embryonic day (E) 10.5, mandibular arch-specific gene expression is normal, as is overall mandible development. These results suggest that while Ednra receptor signaling is crucial for early NCC patterning, subsequent Ednra signaling is not essential for mandible bone development.

摘要

内皮素-A(Ednra)受体发出的信号负责在神经嵴细胞(NCCs)内启动多个信号通路。这种信号启动的缺失可能是在Ednra基因敲除胚胎中观察到颅面缺陷的基础。然而,尚不清楚NCC衍生物中持续的Ednra信号对于下颌骨的后续发育是否是必需的。为了解决这个问题,将含有位于Ednra基因一部分侧翼的loxP重组序列的小鼠与在Dlx5/6增强子元件控制下表达Cre重组酶的转基因小鼠进行杂交。我们发现,虽然在这些Ednra条件性敲除胚胎的下颌弓内,Ednra基因失活在胚胎第10.5天(E10.5)时就可检测到,但下颌弓特异性基因表达正常,下颌骨的整体发育也正常。这些结果表明,虽然Ednra受体信号对于早期NCC模式形成至关重要,但后续的Ednra信号对于下颌骨发育并非必不可少。

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本文引用的文献

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