| Literature DB >> 34133940 |
Shaohe Wang1, Kazue Matsumoto2, Samantha R Lish3, Alexander X Cartagena-Rivera3, Kenneth M Yamada4.
Abstract
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. Published by Elsevier Inc.Entities:
Keywords: E-cadherin; branching morphogenesis; budding morphogenesis; cell-cell adhesion; cell-matrix adhesion; differential adhesion; epithelial morphogenesis; integrin; salivary gland; tissue engineering
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Year: 2021 PMID: 34133940 PMCID: PMC8287763 DOI: 10.1016/j.cell.2021.05.015
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 66.850