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Updated: Aug 1, 2026

Generation of hiPSC-Derived Intestinal Organoids for Developmental and Disease Modelling Applications
Published on: March 8, 2024
An integrated transcriptomic cell atlas of human endoderm-derived organoids
Quan Xu1, Lennard Halle2, Soroor Hediyeh-Zadeh2,3
1Institute of Human Biology (IHB), Roche Pharma Research and Early Development, Roche Innovation Center, Basel, Switzerland. quan.xu@roche.com.
This study integrates nearly one million cells from human endoderm-derived organoids to create a cell atlas. This resource aids in understanding tissue development, disease modeling, and improving organoid protocols.
Area of Science:
- Stem cell biology
- Developmental biology
- Bioinformatics
Background:
- Human stem cells can generate endoderm-derived tissues in vitro.
- These organoid models mimic aspects of human physiology.
- A comprehensive cell atlas is needed for these models.
Purpose of the Study:
- To establish an initial version of a human endoderm-derived organoid cell atlas.
- To integrate single-cell transcriptomes from diverse organoid models.
- To provide a resource for assessing organoid fidelity and disease modeling.
Main Methods:
- Integration of single-cell transcriptomes from 218 samples.
- Analysis of nearly one million cells across various conditions and protocols.
- Harmonization of cell annotations by mapping to primary tissue counterparts.
Main Results:
- Creation of a human endoderm-derived organoid cell atlas.
- Comparison of cell types and states between organoid models.
- Demonstration of atlas utility for assessing perturbations and disease models in intestine and lung organoids.
Conclusions:
- The human endoderm-derived organoid cell atlas centralizes diverse datasets.
- The atlas is valuable for assessing organoid fidelity and characterizing diseased states.
- This resource will streamline organoid protocol development.
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