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Lgr5 marks stem/progenitor cells contributing to epithelial and muscle development in the mouse esophagus

Author

Listed:
  • Lana Kostic

    (Proteos)

  • Carly Leung

    (Proteos)

  • Katzrin Ahmad Murad

    (Proteos)

  • Snezhina Kancheva

    (Proteos)

  • Stefano Perna

    (Experimental Medicine)

  • Bernett Lee

    (Experimental Medicine
    Immunos
    Immunos
    90 Yishun Central)

  • Nick Barker

    (Proteos
    National University of Singapore)

Abstract

The existence and function of Lgr5+ cells within the developing esophagus remains unknown. Here, we document multiple discrete Lgr5+ populations in the developing mouse esophagus, predominantly within nascent epithelial and external muscle layers. Lgr5 expression initially emerges in the developing proximal embryonic epithelium, but progressively extends distally and persists within the distal epithelium of neonates. Fate mapping and ablation analyses reveal a long-term contribution of epithelial Lgr5+ cells to esophageal organogenesis. Additionally, Lgr5-expressing cells are present in the developing external muscle layer, particularly during the development of the striated component. Fate mapping reveals a significant contribution of these embryonic Lgr5+ cells to the adult muscle layer. Embryonic Lgr5+ epithelial cells are also found to be important for regulating epithelial development, serving as a key source of Wnt6, among other ligands, to promote epithelial cell proliferation and formation of epithelial layers. These findings significantly enhance our understanding of esophageal development and shed light on the involvement of Lgr5+ stem/progenitor cells during organogenesis. Importantly, this study lays the foundation for investigating esophageal diseases related to the Lgr5+ stem/progenitor cell pool.

Suggested Citation

  • Lana Kostic & Carly Leung & Katzrin Ahmad Murad & Snezhina Kancheva & Stefano Perna & Bernett Lee & Nick Barker, 2024. "Lgr5 marks stem/progenitor cells contributing to epithelial and muscle development in the mouse esophagus," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-51559-4
    DOI: 10.1038/s41467-024-51559-4
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    References listed on IDEAS

    as
    1. Mohammad Faujul Kabir & Adam L. Karami & Ricardo Cruz-Acuña & Alena Klochkova & Reshu Saxena & Anbin Mu & Mary Grace Murray & Jasmine Cruz & Annie D. Fuller & Margarette H. Clevenger & Kumaraswamy Nai, 2022. "Single cell transcriptomic analysis reveals cellular diversity of murine esophageal epithelium," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
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    3. Ryo Seishima & Carly Leung & Swathi Yada & Katzrin Bte Ahmed Murad & Liang Thing Tan & Amin Hajamohideen & Si Hui Tan & Hideki Itoh & Kazuhiro Murakami & Yoshihiro Ishida & Satoshi Nakamizo & Yusuke Y, 2019. "Neonatal Wnt-dependent Lgr5 positive stem cells are essential for uterine gland development," Nature Communications, Nature, vol. 10(1), pages 1-17, December.
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