Xu Jingyue, Liu Han, Lan Yu, Aronow Bruce J, Kalinichenko Vladimir V, Jiang Rulang
Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
Division of Plastic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
PLoS Genet. 2016 Jan 8;12(1):e1005769. doi: 10.1371/journal.pgen.1005769. eCollection 2016 Jan.
Cleft palate is among the most common birth defects in humans. Previous studies have shown that Shh signaling plays critical roles in palate development and regulates expression of several members of the forkhead-box (Fox) family transcription factors, including Foxf1 and Foxf2, in the facial primordia. Although cleft palate has been reported in mice deficient in Foxf2, whether Foxf2 plays an intrinsic role in and how Foxf2 regulates palate development remain to be elucidated. Using Cre/loxP-mediated tissue-specific gene inactivation in mice, we show that Foxf2 is required in the neural crest-derived palatal mesenchyme for normal palatogenesis. We found that Foxf2 mutant embryos exhibit altered patterns of expression of Shh, Ptch1, and Shox2 in the developing palatal shelves. Through RNA-seq analysis, we identified over 150 genes whose expression was significantly up- or down-regulated in the palatal mesenchyme in Foxf2-/- mutant embryos in comparison with control littermates. Whole mount in situ hybridization analysis revealed that the Foxf2 mutant embryos exhibit strikingly corresponding patterns of ectopic Fgf18 expression in the palatal mesenchyme and concomitant loss of Shh expression in the palatal epithelium in specific subdomains of the palatal shelves that correlate with where Foxf2, but not Foxf1, is expressed during normal palatogenesis. Furthermore, tissue specific inactivation of both Foxf1 and Foxf2 in the early neural crest cells resulted in ectopic activation of Fgf18 expression throughout the palatal mesenchyme and dramatic loss of Shh expression throughout the palatal epithelium. Addition of exogenous Fgf18 protein to cultured palatal explants inhibited Shh expression in the palatal epithelium. Together, these data reveal a novel Shh-Foxf-Fgf18-Shh circuit in the palate development molecular network, in which Foxf1 and Foxf2 regulate palatal shelf growth downstream of Shh signaling, at least in part, by repressing Fgf18 expression in the palatal mesenchyme to ensure maintenance of Shh expression in the palatal epithelium.
腭裂是人类最常见的出生缺陷之一。先前的研究表明,Shh信号在腭部发育中起关键作用,并调节面部原基中叉头框(Fox)家族转录因子的几个成员的表达,包括Foxf1和Foxf2。虽然在Foxf2缺陷的小鼠中已报道有腭裂,但Foxf2是否在腭部发育中起内在作用以及Foxf2如何调节腭部发育仍有待阐明。利用Cre/loxP介导的小鼠组织特异性基因失活,我们发现Foxf2在神经嵴衍生的腭间充质中是正常腭发育所必需的。我们发现Foxf2突变胚胎在发育中的腭突中Shh、Ptch1和Shox2的表达模式发生改变。通过RNA测序分析,我们鉴定出150多个基因,与对照同窝小鼠相比,其在Foxf2 - / - 突变胚胎的腭间充质中的表达显著上调或下调。整体原位杂交分析显示,Foxf2突变胚胎在腭突的特定亚区域的腭间充质中表现出异位Fgf18表达的显著相应模式,以及腭上皮中Shh表达的伴随缺失,这与正常腭发育过程中Foxf2而非Foxf1的表达位置相关。此外,早期神经嵴细胞中Foxf1和Foxf2的组织特异性失活导致整个腭间充质中Fgf18表达的异位激活以及整个腭上皮中Shh表达的显著丧失。向培养的腭外植体中添加外源性Fgf18蛋白可抑制腭上皮中Shh的表达。总之,这些数据揭示了腭发育分子网络中一个新的Shh - Foxf - Fgf18 - Shh回路,其中Foxf1和Foxf2至少部分地通过抑制腭间充质中Fgf18的表达来调节Shh信号下游的腭突生长,以确保腭上皮中Shh表达的维持。