Deep visual proteomics reveals an in vivo-like phenotype of orthotopically transplanted human colon organoids

Intestinal epithelial damage predisposes to disorders like inflammatory bowel disease (IBD), with organoid transplantation emerging as a potential treatment. However, it is not known how well organoids recapitulate in vivo intestinal epithelial cells (IECs). We employed deep visual proteomics (DVP), integrating AI-guided cell classification, laser microdissection, and ultra-high-sensitivity proteomics at the single-cell level to generate an in-depth proteome resource of IECs directly isolated from the human colon and organoids. While in vitro organoids display high proliferation and low functional signatures, xenotransplantation induces a remarkable shift toward an in vivo-like phenotype. We recapitulated this transition by modifying culture conditions. Our data provide a comprehensive spatial proteomics resource and validate xenotransplanted organoids as suitable models for studying human IEC behavior with unprecedented molecular detail and demonstrate their clinical potential for patients with IBD and other intestinal disorders. A record of this paper's transparent peer review process is included in the supplemental information.

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Publication Details

Journal
Cell Systems
Published
2025-09-01
DOI
https://doi.org/10.1016/j.cels.2025.101396
Citations
2
Primary Topic
Cancer Cells and Metastasis
Type
article
Field-Weighted Citation Impact
2.09
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article

Deep visual proteomics reveals an in vivo-like phenotype of orthotopically transplanted human colon organoids

Theresa Louise Boye, Ole Haagen Nielsen, Toshiro Sato, Ditte L. Clement et al.
2 citations
Cell Systems
Cancer Cells and Metastasis
2.09
article

Deep visual proteomics reveals an in vivo-like phenotype of orthotopically transplanted human colon organoids

Theresa Louise Boye, Ole Haagen Nielsen, Toshiro Sato, Ditte L. Clement, Alexandra Brand, Casper Steenholdt, Florian A. Rosenberger, Kadi Lõhmussaar, Martti Maimets, Hjalte List Larsen, Andreas Mund, Jonathan Skov, Kim B. Jensen, Frederik Post, Sonja Kabatnik, Sophia Steigerwald, Annika Hausmann, Matthias Mann, Gabriela Jez
article en
2 citations

Abstract

Intestinal epithelial damage predisposes to disorders like inflammatory bowel disease (IBD), with organoid transplantation emerging as a potential treatment. However, it is not known how well organoids recapitulate in vivo intestinal epithelial cells (IECs). We employed deep visual proteomics (DVP), integrating AI-guided cell classification, laser microdissection, and ultra-high-sensitivity proteomics at the single-cell level to generate an in-depth proteome resource of IECs directly isolated from the human colon and organoids. While in vitro organoids display high proliferation and low functional signatures, xenotransplantation induces a remarkable shift toward an in vivo-like phenotype. We recapitulated this transition by modifying culture conditions. Our data provide a comprehensive spatial proteomics resource and validate xenotransplanted organoids as suitable models for studying human IEC behavior with unprecedented molecular detail and demonstrate their clinical potential for patients with IBD and other intestinal disorders. A record of this paper's transparent peer review process is included in the supplemental information.

Cell SystemsVol. 16(9)
University of Copenhagen (DK), University of Southern Denmark (DK), Keio University (JP), Novo Nordisk Foundation (DK), Odense University Hospital (DK), Herlev Hospital (DK), Max Planck Institute of Biochemistry (DE)
Openalex Percentile: Top 10%
Cancer Cells and Metastasis
2.09
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