4.7 Article

Transplantation of intestinal organoids into a mouse model of colitis

期刊

NATURE PROTOCOLS
卷 17, 期 3, 页码 649-+

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NATURE PORTFOLIO
DOI: 10.1038/s41596-021-00658-3

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资金

  1. MEXT/JSPS KAKENHI [18K15743, 20H03657, 19H01050, 19H03634]
  2. Young Innovative Medical Science Unit (TMDU), Naoki Tsuchiya Research Grant, Japan Agency for Medical Research and Development (AMED) [20bm0704029h0003, 20bm0304001h0008, 20bk0104008h0003, 20bm0404055h0002]
  3. Marie Curie fellowship programme [625238]
  4. DFF mobilex programme [1333-00130B]
  5. European Union [KBJ - ERCCoG682665]
  6. Novo Nordisk Foundation Center for Stem Cell Medicine by Novo Nordisk Foundation [NNF17CC0027852, NNF21CC0073729]
  7. Grants-in-Aid for Scientific Research [18K15743, 19H03634, 19H01050, 20H03657] Funding Source: KAKEN

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This article provides a detailed description of how to orthotopically transplant epithelial organoids into the colon of recipient mice. The protocol has been successfully applied to organoids derived from different sources and states, and has been used for disease modeling and regenerative medicine research.
Intestinal organoids are fundamental in vitro tools that have enabled new research opportunities in intestinal stem cell research. Organoids can also be transplanted in vivo, which enables them to probe stem cell potential and be used for disease modeling and as a preclinical tool in regenerative medicine. Here we describe in detail how to orthotopically transplant epithelial organoids into the colon of recipient mice. In this assay, epithelial injury is initiated at the distal part of colon by the administration of dextran sulfate sodium, and organoids are infused into the luminal space via the anus. The infused organoids subsequently attach to the injured region and rebuild a donor-derived epithelium. The steps for cell infusion can be completed in 10 min. The assay has been applied successfully to organoids derived from both wild-type and genetically altered epithelial cells from adult colonic and small intestinal epithelium, as well as fetal small intestine. This is a versatile protocol, providing the technical basis for transplantation following alternative colonic injury models. It has been used previously for functional assays to probe cellular potential, and formed the basis for the first in-human clinical trial using colonic organoid transplantation therapy for intractable cases of ulcerative colitis. An approach to studying epithelia derived from organoids of either fetal or adult state and from both the small intestine and colon via transplantation into animals in which the colon has been damaged following administration of dextran sulfate sodium.

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