Department of Craniofacial Development and Comprehensive Biomedical Research Centre, Dental Institute, King's College London, UK.
Dev Biol. 2012 May 1;365(1):61-70. doi: 10.1016/j.ydbio.2012.02.009. Epub 2012 Feb 14.
Thickening and the subsequent invagination of the epithelium are an important initial step in ectodermal organ development. Ikkα has been shown to play a critical role in controlling epithelial growth, since Ikkα mutant mice show protrusions (evaginations) of incisor tooth, whisker and hair follicle epithelium rather than invagination. We show here that mutation of the Interferon regulatory factor (Irf) family, Irf6 also results in evagination of incisor epithelium. In common with Ikkα mutants, Irf6 mutant evagination occurs in a NF-κB-independent manner and shows the same molecular changes as those in Ikkα mutants. Irf6 thus also plays a critical role in regulating epithelial invagination. In addition, we also found that canonical Wnt signaling is upregulated in evaginated incisor epithelium of both Ikkα and Irf6 mutant embryos.
上皮细胞的增厚和随后的内陷是外胚层器官发育的重要初始步骤。已经表明 Ikkα 在控制上皮细胞生长中起着关键作用,因为 Ikkα 突变小鼠的门牙、触须和毛囊上皮出现突起(外翻),而不是内陷。我们在这里表明,干扰素调节因子(Irf)家族的突变 Irf6 也导致门牙上皮的外翻。与 Ikkα 突变体一样,Irf6 突变体的外翻发生在 NF-κB 独立的方式下,并显示出与 Ikkα 突变体相同的分子变化。因此,Irf6 也在调节上皮内陷中起着关键作用。此外,我们还发现,经典 Wnt 信号在 Ikkα 和 Irf6 突变胚胎的外翻门牙上皮中上调。