Cell Biology Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
Cell Biology Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
Cell. 2021 Jul 8;184(14):3702-3716.e30. doi: 10.1016/j.cell.2021.05.015. Epub 2021 Jun 15.
Many embryonic organs undergo epithelial morphogenesis to form tree-like hierarchical structures. However, it remains unclear what drives the budding and branching of stratified epithelia, such as in the embryonic salivary gland and pancreas. Here, we performed live-organ imaging of mouse embryonic salivary glands at single-cell resolution to reveal that budding morphogenesis is driven by expansion and folding of a distinct epithelial surface cell sheet characterized by strong cell-matrix adhesions and weak cell-cell adhesions. Profiling of single-cell transcriptomes of this epithelium revealed spatial patterns of transcription underlying these cell adhesion differences. We then synthetically reconstituted budding morphogenesis by experimentally suppressing E-cadherin expression and inducing basement membrane formation in 3D spheroid cultures of engineered cells, which required β1-integrin-mediated cell-matrix adhesion for successful budding. Thus, stratified epithelial budding, the key first step of branching morphogenesis, is driven by an overall combination of strong cell-matrix adhesion and weak cell-cell adhesion by peripheral epithelial cells.
许多胚胎器官经历上皮形态发生,形成树状层次结构。然而,驱动分层上皮(如胚胎唾液腺和胰腺)出芽和分支的原因仍不清楚。在这里,我们以单细胞分辨率对小鼠胚胎唾液腺进行了活体器官成像,揭示了出芽形态发生是由具有强细胞-基质粘附和弱细胞-细胞粘附的独特上皮表面细胞片的扩展和折叠驱动的。对该上皮细胞的单细胞转录组进行分析,揭示了这些细胞粘附差异背后的转录空间模式。然后,我们通过在工程细胞的 3D 球体培养物中实验性抑制 E-钙粘蛋白表达和诱导基底膜形成,综合重建了出芽形态发生,这需要β1-整合素介导的细胞-基质粘附才能成功出芽。因此,分层上皮出芽是分支形态发生的关键第一步,由外围上皮细胞的强细胞-基质粘附和弱细胞-细胞粘附的总体组合驱动。