1 Manchester Academic Health Sciences Centre, University of Manchester, Manchester, UK.
2 Current address: Human Genetics, Life Sciences, University of Nottingham, University Park, Nottingham, UK.
J Dent Res. 2018 Dec;97(13):1485-1493. doi: 10.1177/0022034518785336. Epub 2018 Jul 5.
Cleft palate is a common birth defect that frequently occurs in human congenital malformations caused by mutations in components of the Sonic Hedgehog (S HH) signaling cascade. Shh is expressed in dynamic, spatiotemporal domains within epithelial rugae and plays a key role in driving epithelial-mesenchymal interactions that are central to development of the secondary palate. However, the gene regulatory networks downstream of Hedgehog (Hh) signaling are incompletely characterized. Here, we show that ectopic Hh signaling in the palatal mesenchyme disrupts oral-nasal patterning of the neural crest cell-derived ectomesenchyme of the palatal shelves, leading to defective palatine bone formation and fully penetrant cleft palate. We show that a series of Fox transcription factors, including the novel direct target Foxl1, function downstream of Hh signaling in the secondary palate. Furthermore, we demonstrate that Wnt/bone morphogenetic protein (BMP) antagonists, in particular Sostdc1, are positively regulated by Hh signaling, concomitant with downregulation of key regulators of osteogenesis and BMP signaling effectors. Our data demonstrate that ectopic Hh-Smo signaling downregulates Wnt/BMP pathways, at least in part by upregulating Sostdc1, resulting in cleft palate and defective osteogenesis.
腭裂是一种常见的出生缺陷,常发生于人类先天性畸形,由 Sonic Hedgehog (S HH) 信号级联反应成分中的突变引起。Shh 在上皮嵴的动态、时空域中表达,在驱动上皮-间充质相互作用中发挥关键作用,而这些相互作用是次级腭发育的核心。然而,Hedgehog (Hh) 信号下游的基因调控网络尚未完全描述。在这里,我们表明,腭间质中的异位 Hh 信号会破坏腭突衍生的外胚间充质的口腔-鼻腔模式,导致腭骨形成缺陷和完全穿透性腭裂。我们表明,一系列 Fox 转录因子,包括新的直接靶标 Foxl1,在次级腭中作为 Hh 信号的下游发挥作用。此外,我们证明 Wnt/骨形态发生蛋白 (BMP) 拮抗剂,特别是 Sostdc1,受 Hh 信号的正调控,同时下调成骨和 BMP 信号效应物的关键调节剂。我们的数据表明,异位 Hh-Smo 信号下调 Wnt/BMP 途径,至少部分是通过上调 Sostdc1 导致腭裂和骨形成缺陷。