Dictionary of human intestinal organoid responses to secreted niche factors at single cell resolution

The intestinal epithelium plays a critical role in health and disease, yet the impact of microenvironmental cues in diseased contexts, such as inflammatory bowel disease (IBD), remains poorly defined. To address this gap, we first benchmarked human colonic organoid injury models against IBD tissue and established a disease-relevant model of inflammation using inflammatory cytokines. Using this system, we built a dictionary of epithelial responses to 79 secreted niche factors at single cell resolution via donor-pooled, multiplexed single cell RNA-sequencing. The comprehensive nature of our atlas allowed us to map relationships between perturbations, infer the function of less characterized ligands, and identify cell type-specific perturbed pathways. Finally, we established the relevance of organoid-derived gene programs by mapping them to single cell and spatial atlases of human IBD tissue. Our resource offers a global view of epithelial responses to microenvironmental cues, offering insights into epithelial homeostasis and repair mechanisms in IBD.

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Publication Details

Journal
Nature Communications
Published
2026-01-09
DOI
https://doi.org/10.1038/s41467-025-68247-6
Primary Topic
Single-cell and spatial transcriptomics
Type
article
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article

Dictionary of human intestinal organoid responses to secreted niche factors at single cell resolution

Devan Phillips, Runmin Wei, Meghan M. Capeling, Elizabeth Skippington et al.
Nature Communications
Single-cell and spatial transcriptomics
article

Dictionary of human intestinal organoid responses to secreted niche factors at single cell resolution

Devan Phillips, Runmin Wei, Meghan M. Capeling, Elizabeth Skippington, Caden W. Sweet, Lisa McGinnis, Verónica López, Kazeera Aliar, Sandra Rost, Loryn Holokai, Zora Modrusan, Conrad Foo, Xinming Tong, Jing Li, Mary Keir, Sharmila Chatterjee, Bob Chen, Orit Rozenblatt-Rosen, Elisa Penna, Michelle B. Chen
article en

Abstract

The intestinal epithelium plays a critical role in health and disease, yet the impact of microenvironmental cues in diseased contexts, such as inflammatory bowel disease (IBD), remains poorly defined. To address this gap, we first benchmarked human colonic organoid injury models against IBD tissue and established a disease-relevant model of inflammation using inflammatory cytokines. Using this system, we built a dictionary of epithelial responses to 79 secreted niche factors at single cell resolution via donor-pooled, multiplexed single cell RNA-sequencing. The comprehensive nature of our atlas allowed us to map relationships between perturbations, infer the function of less characterized ligands, and identify cell type-specific perturbed pathways. Finally, we established the relevance of organoid-derived gene programs by mapping them to single cell and spatial atlases of human IBD tissue. Our resource offers a global view of epithelial responses to microenvironmental cues, offering insights into epithelial homeostasis and repair mechanisms in IBD.

Nature CommunicationsVol. 17(1)
Gene Therapy Laboratory (FR)
Openalex Percentile: Top 93%
Single-cell and spatial transcriptomics
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