首页> 外文期刊>The Journal of Clinical Investigation: The Official Journal of the American Society for Clinical Investigation >Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate.
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Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate.

机译:Fgf10/Fgfr2b配位的上皮-间充质相互作用的破坏导致腭裂。

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摘要

Classical research has suggested that early palate formation develops via epithelial-mesenchymal interactions, and in this study we reveal which signals control this process. Using Fgf10-/-, FGF receptor 2b-/- (Fgfr2b-/-), and Sonic hedgehog (Shh) mutant mice, which all exhibit cleft palate, we show that Shh is a downstream target of Fgf10/Fgfr2b signaling. Our results demonstrate that mesenchymal Fgf10 regulates the epithelial expression of Shh, which in turn signals back to the mesenchyme. This was confirmed by demonstrating that cell proliferation is decreased not only in the palatal epithelium but also in the mesenchyme of Fgfr2b-/- mice. These results reveal a new role for Fgf signaling in mammalian palate development. We show that coordinated epithelial-mesenchymal interactions are essential during the initial stages of palate development and require an Fgf-Shh signaling network.
机译:经典研究表明,早期上颚形成是通过上皮-间充质相互作用发展起来的,在这项研究中,我们揭示了哪些信号控制了这一过程。使用 Fgf10-/-、FGF 受体 2b-/- (Fgfr2b-/-) 和 Sonic hedgehog (Shh) 突变小鼠,它们都表现出腭裂,我们表明 Shh 是 Fgf10/Fgfr2b 信号传导的下游靶标。我们的结果表明,间充质 Fgf10 调节 Shh 的上皮表达,而 Shh 又向间充质发出信号。通过证明不仅腭上皮细胞增殖减少,而且Fgfr2b-/-小鼠间充质中的细胞增殖减少,证实了这一点。这些结果揭示了Fgf信号转导在哺乳动物上颚发育中的新作用。我们发现,协调的上皮-间充质相互作用在上颚发育的初始阶段是必不可少的,并且需要 Fgf-Shh 信号网络。

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