Ray Heather J, Niswander Lee A
Department of Pediatrics, Cell Biology Stem Cells and Development Graduate Program, University of Colorado Anschutz Medical Campus and Children's Hospital Colorado, Aurora, CO 80045, USA.
Department of Pediatrics, Cell Biology Stem Cells and Development Graduate Program, University of Colorado Anschutz Medical Campus and Children's Hospital Colorado, Aurora, CO 80045, USA
Development. 2016 Apr 1;143(7):1192-204. doi: 10.1242/dev.129825. Epub 2016 Feb 22.
The transcription factor grainyhead-like 2 (GRHL2) is expressed in non-neural ectoderm (NNE) and Grhl2 loss results in fully penetrant cranial neural tube defects (NTDs) in mice. GRHL2 activates expression of several epithelial genes; however, additional molecular targets and functional processes regulated by GRHL2 in the NNE remain to be determined, as well as the underlying cause of the NTDs in Grhl2 mutants. Here, we find that Grhl2 loss results in abnormal mesenchymal phenotypes in the NNE, including aberrant vimentin expression and increased cellular dynamics that affects the NNE and neural crest cells. The resulting loss of NNE integrity contributes to an inability of the cranial neural folds to move toward the midline and results in NTD. Further, we identified Esrp1, Sostdc1, Fermt1, Tmprss2 and Lamc2 as novel NNE-expressed genes that are downregulated in Grhl2 mutants. Our in vitro assays show that they act as suppressors of the epithelial-to-mesenchymal transition (EMT). Thus, GRHL2 promotes the epithelial nature of the NNE during the dynamic events of neural tube formation by both activating key epithelial genes and actively suppressing EMT through novel downstream EMT suppressors.
转录因子颗粒头样蛋白2(GRHL2)在非神经外胚层(NNE)中表达,Grhl2缺失会导致小鼠出现完全显性的颅神经管缺陷(NTDs)。GRHL2可激活多个上皮基因的表达;然而,GRHL2在NNE中调控的其他分子靶点和功能过程仍有待确定,Grhl2突变体中NTDs的潜在原因也尚不明确。在此,我们发现Grhl2缺失会导致NNE中出现异常的间充质表型,包括波形蛋白表达异常以及细胞动态变化增加,这会影响NNE和神经嵴细胞。由此导致的NNE完整性丧失致使颅神经褶无法向中线移动,进而导致NTD。此外,我们鉴定出Esrp1、Sostdc1、Fermt1、Tmprss2和Lamac2是在NNE中表达的新基因,它们在Grhl2突变体中表达下调。我们的体外实验表明,它们可作为上皮-间充质转化(EMT)的抑制因子。因此,GRHL2在神经管形成的动态过程中,通过激活关键上皮基因并通过新的下游EMT抑制因子积极抑制EMT,来促进NNE的上皮特性。