TY - JOUR
T1 - In Vivo Intestinal Research Using Organoid Transplantation
AU - Sugimoto, Shinya
AU - Kobayashi, Eiji
AU - Kanai, Takanori
AU - Sato, Toshiro
N1 - Funding Information:
This work was supported by the Japan Agency for Medical Research and Development (AMED) (grant numbers JP21ek0109523 and JP21bm0704069), AMED-CREST (grant number JP18gm1210001), Japan Society for the Promotion of Science (grant numbers JP21K19540 and JP20H03746), the Mochida Memorial Foundation for Medical and Pharmaceutical Research, the Takeda Science Foundation, and Keio Gijuku Fukuzawa Memorial Fund for the Advancement of Education and Research.
Publisher Copyright:
© 2022 by The Keio Journal of Medicine.
PY - 2022
Y1 - 2022
N2 - Our understanding of the biology of the intestinal epithelium has advanced since the establishment of an organoid culture system. Although organoids have enabled investigation of the mechanism of self-renewal of human intestinal stem cells in vitro, it remains difficult to clarify the behavior of human normal and diseased intestinal epithelium in vivo. Recently, we developed a xenotransplantation system in which human intestinal organoids are engrafted onto epithelium-depleted mouse colons. This xenograft recapitulated the original tissue structures. Upon xenotransplantation, normal colon organoids developed normal colon crypt structures without tumorigenesis, whereas tumor-derived organoids formed colonic tumors resembling the original tumors. The non-tumorigenicity of human intestinal organoids highlights the safety of organoid-based regenerative medicine. As an example of regenerative medicine for short bowel syndrome, we devised a unique organ-repurposing approach to convert colons into small intestines by organoid transplantation. In this approach, the transplanted rat small intestinal organ-oids not only engrafted onto the rat colons but also remodeled the colon subepithelial structures into a small intestine-like conformation. Luminal flow accelerated the maturation of villi in the small intes-tine, which promoted the formation of a lymphovascular network mimicking lacteals. In this review, we provide an overview of recent advances in gastrointestinal organoid transplantation and share our understanding of human disease biology and regenerative medicine derived from these studies.
AB - Our understanding of the biology of the intestinal epithelium has advanced since the establishment of an organoid culture system. Although organoids have enabled investigation of the mechanism of self-renewal of human intestinal stem cells in vitro, it remains difficult to clarify the behavior of human normal and diseased intestinal epithelium in vivo. Recently, we developed a xenotransplantation system in which human intestinal organoids are engrafted onto epithelium-depleted mouse colons. This xenograft recapitulated the original tissue structures. Upon xenotransplantation, normal colon organoids developed normal colon crypt structures without tumorigenesis, whereas tumor-derived organoids formed colonic tumors resembling the original tumors. The non-tumorigenicity of human intestinal organoids highlights the safety of organoid-based regenerative medicine. As an example of regenerative medicine for short bowel syndrome, we devised a unique organ-repurposing approach to convert colons into small intestines by organoid transplantation. In this approach, the transplanted rat small intestinal organ-oids not only engrafted onto the rat colons but also remodeled the colon subepithelial structures into a small intestine-like conformation. Luminal flow accelerated the maturation of villi in the small intes-tine, which promoted the formation of a lymphovascular network mimicking lacteals. In this review, we provide an overview of recent advances in gastrointestinal organoid transplantation and share our understanding of human disease biology and regenerative medicine derived from these studies.
KW - epithelium replacement
KW - intestinal organoid
KW - organoid transplantation
KW - regenerative medicine
KW - xenograft
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U2 - 10.2302/kjm.2022-0019-IR
DO - 10.2302/kjm.2022-0019-IR
M3 - Article
C2 - 36450523
AN - SCOPUS:85144637164
SN - 0022-9717
VL - 71
SP - 73
EP - 81
JO - Keio Journal of Medicine
JF - Keio Journal of Medicine
IS - 4
ER -