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Mesenchymal-epithelial interaction regulates gastrointestinal tract development in mouse embryos.
Zhao, Lianzheng; Song, Wanlu; Chen, Ye-Guang.
Affiliation
  • Zhao L; The State Key Laboratory of Membrane Biology, Tsinghua-Peking Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China.
  • Song W; The State Key Laboratory of Membrane Biology, Tsinghua-Peking Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China.
  • Chen YG; The State Key Laboratory of Membrane Biology, Tsinghua-Peking Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China; Guangzhou Laboratory, Guangzhou, China. Electronic address: ygchen@tsinghua.edu.cn.
Cell Rep ; 40(2): 111053, 2022 07 12.
Article in En | MEDLINE | ID: mdl-35830795
After gut tube patterning in early embryos, the cellular and molecular changes of developing stomach and intestine remain largely unknown. Here, combining single-cell RNA sequencing and spatial RNA sequencing, we construct a spatiotemporal transcriptomic landscape of the mouse stomach and intestine during embryonic days E9.5-E15.5. Several subpopulations are identified, including Lox+ stomach mesenchyme, Aldh1a3+ small-intestinal mesenchyme, and Adamdec1+ large-intestinal mesenchyme. The regionalization and heterogeneity of both the epithelium and the mesenchyme can be traced back to E9.5. The spatiotemporal distributions of cell clusters and the mesenchymal-epithelial interaction analysis indicate that a coordinated development of the epithelium and mesenchyme contribute to the stomach regionalization, intestine segmentation, and villus formation. Using the gut tube-derived organoids, we find that the cell fate of the foregut and hindgut can be switched by the regional niche factors, including fibroblast growth factors (FGFs) and retinoic acid (RA). This work lays a foundation for further dissection of the mechanisms governing this process.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Endoderm / Mesoderm Type of study: Prognostic_studies Limits: Animals Language: En Journal: Cell Rep Year: 2022 Document type: Article Affiliation country: China Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Endoderm / Mesoderm Type of study: Prognostic_studies Limits: Animals Language: En Journal: Cell Rep Year: 2022 Document type: Article Affiliation country: China Country of publication: United States