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Organoid Derivation and Orthotopic Xenotransplantation for Studying Human Intestinal Stem Cell Dynamics

Protocol
Part of the Methods in Molecular Biology book series (MIMB, volume 2171)

Abstract

Intestinal stem cells continuously self-renew throughout life to maintain gut homeostasis. With the advent of the organoid culture system, we are now able to indefinitely expand healthy and diseased tissue-derived human intestinal stem cells in vitro and use them for various applications. Nonetheless, investigating the behavior of human intestinal stem cells in vivo still remains challenging. We recently developed an orthotopic xenotransplantation system that realizes in vivo reconstruction of human intestinal epithelial tissue with preserved stem cell hierarchy by engrafting human normal colon organoids onto the mouse colon surface. We also introduced new growth factors, namely, insulin-like growth factor-1 (IGF-1) and fibroblast growth factor-2 (FGF-2), into the culture condition for human intestinal organoids that significantly increase scalability and transfectability of the organoids. By integrating these recent advances, we organized a tissue-oriented platform encompassing derivation of patient-derived intestinal organoids and their orthotopic xenotransplantation. The research platform based on orthotopic xenotransplantation of human intestinal organoids provides a powerful tool for studying human intestinal stem cell biology in native tissue-relevant contexts as well as for establishing novel disease modeling systems.

Key words

Intestinal stem cells LGR5 Crypt isolation Organoid culture Mini-gut Colon Human Electroporation Orthotopic transplantation Endoscopy 

Notes

Acknowledgments

This work was in part supported by the Research Center Network for Realization of Regenerative Medicine project from the Japan Agency for Medical Research and Development.

References

  1. 1.
    Sato T, Vries RG, Snippert HJ et al (2009) Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche. Nature 459:262–265PubMedPubMedCentralGoogle Scholar
  2. 2.
    Sato T, Stange DE, Ferrante M et al (2011) Long-term expansion of epithelial organoids from human colon, adenoma, adenocarcinoma, and Barrett's epithelium. Gastroenterology 141:1762–1772PubMedGoogle Scholar
  3. 3.
    Mihara E, Hirai H, Yamamoto H et al (2016) Active and water-soluble form of lipidated Wnt protein is maintained by a serum glycoprotein afamin/alpha-albumin. Elife 5:e11621.  https://doi.org/10.7554/eLife.11621CrossRefPubMedPubMedCentralGoogle Scholar
  4. 4.
    Fujii M, Matano M, Toshimitsu K et al (2018) Human intestinal organoids maintain self-renewal capacity and cellular diversity in niche-inspired culture condition. Cell Stem Cell 23:787–793.e6PubMedGoogle Scholar
  5. 5.
    Sugimoto S, Ohta Y, Fujii M et al (2018) Reconstruction of the human colon epithelium in vivo. Cell Stem Cell 22:171–176.e5PubMedGoogle Scholar
  6. 6.
    Fukuda M, Mizutani T, Mochizuki W et al (2014) Small intestinal stem cell identity is maintained with functional Paneth cells in heterotopically grafted epithelium onto the colon. Genes Dev 28:1752–1757PubMedPubMedCentralGoogle Scholar
  7. 7.
    Fujii M, Matano M, Nanki K et al (2015) Efficient genetic engineering of human intestinal organoids using electroporation. Nat Protoc 10:1474–1485PubMedGoogle Scholar
  8. 8.
    Seino T, Kawasaki S, Shimokawa M et al (2018) Human pancreatic tumor Organoids reveal loss of stem cell niche factor dependence during disease progression. Cell Stem Cell 22:454–467.e6PubMedPubMedCentralGoogle Scholar
  9. 9.
    Ootani A, Li X, Sangiorgi E et al (2009) Sustained in vitro intestinal epithelial culture within a Wnt-dependent stem cell niche. Nat Med 15:701–706PubMedPubMedCentralGoogle Scholar
  10. 10.
    Farin HF, Van Es JH, Clevers H (2012) Redundant sources of Wnt regulate intestinal stem cells and promote formation of Paneth cells. Gastroenterology 143:1518–1529.e7PubMedGoogle Scholar
  11. 11.
    Koo BK, Stange DE, Sato T et al (2011) Controlled gene expression in primary Lgr5 organoid cultures. Nat Methods 9:81–83PubMedGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2020

Authors and Affiliations

  1. 1.Department of Organoid MedicineKeio University School of MedicineShinjuku-kuJapan
  2. 2.Department of GastroenterologyKeio University School of MedicineShinjuku-kuJapan

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