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Updated: Jun 16, 2026

Combining Human Organoids and Organ-on-a-Chip Technology to Model Intestinal Region-Specific Functionality
Published on: May 5, 2022
Current Practices and Considerations for Benchmarking Human Gastrointestinal Organoids
Monica E Brown1, Antoine R Gleizes2, Qianhui Yu3
1Department of Cell and Developmental Biology, Vanderbilt University, Nashville, Tennessee; Epithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee; Center for Computational Systems Biology, Vanderbilt University, Nashville, Tennessee.
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Since the first reports of organoids cultured from primary human small intestine and colonic epithelium in 2011, these systems have held considerable potential to accelerate our understanding of gastrointestinal biology and disease. Improvements in tissue isolation and culture conditions for primary tissue organoids, as well as the parallel development of protocols for generating organoids from pluripotent cells, have made organoid research increasingly accessible over the last 15 years. As organoids emerge as bona fide model systems, there is a growing need to understand and evaluate the accuracy and limitations of their ability to represent different aspects of gastrointestinal biology, both within and across laboratories and experimental contexts. In this Guiding Principles commentary, we outline the current state of the field and challenges for benchmarking human small intestinal and colonic organoids against native gastrointestinal tract biology. We outline a conceptual framework for approaching organoid benchmarking at multiple scales, review current approaches and efforts in assaying similarities between organoids and their source tissues, and discuss the "next frontiers" for validating organoids as reproducible and high-fidelity models of the human gastrointestinal tract.

