4.5 Article

Drivers of transcriptional variance in human intestinal epithelial organoids

Journal

PHYSIOLOGICAL GENOMICS
Volume 53, Issue 11, Pages 486-508

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physiolgenomics.00061.2021

Keywords

colonoids; enteroids; extracellular matrix; intestinal organoids; transcriptome

Funding

  1. National Institute of Diabetes and Digestive and Kidney Disorders (NIDDK)
  2. National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health [U19AI144297, P30DK056338, R01DK118904, U01DK103117, R01DK112365, U19AI116497]
  3. Howard Hughes Medical Institute Gilliam Fellowship
  4. Baylor Research Advocates for Student Scientists (BRASS)

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The study investigated the impact of common variations in culture methods on the transcriptome of human intestinal epithelial organoids, finding that substrate and format had the largest effects on transcriptomic variation, while patient heterogeneity and specific experimental manipulations had smaller effects. Results show that variations in culture conditions can significantly influence intestinal organoids and should be considered when designing experiments and comparing results between laboratories.
Human intestinal epithelial organoids (enteroids and colonoids) are tissue cultures used for understanding the physiology of the human intestinal epithelium. Here, we explored the effect on the transcriptome of common variations in culture methods, including extracellular matrix substrate, format, tissue segment, differentiation status, and patient heterogeneity. RNA-sequencing data-sets from 276 experiments performed on 37 human enteroid and colonoid lines from 29 patients were aggregated from several groups in the Texas Medical Center. DESeq2 and gene set enrichment analysis (GSEA) were used to identify differentially expressed genes and enriched pathways. PERMANOVA, Pearson's correlation, and dendrogram analysis of the data originally indicated three tiers of influence of culture methods on transcriptomic variation: substrate (collagen vs. Matrigel) and format (3-D, transwell, and monolayer) had the largest effect; segment of origin (duodenum, jejunum, ileum, colon) and differentiation status had a moderate effect; and patient heterogeneity and specific experimental manipulations (e.g., pathogen infection) had the smallest effect. GSEA identified hundreds of pathways that varied between culture methods, such as IL1 cytokine signaling enriched in transwell versus monolayer cultures and E2F target genes enriched in collagen versus Matrigel cultures. The transcriptional influence of the format was furthermore validated in a synchronized experiment performed with various format-substrate combinations. Surprisingly, large differences in organoid transcriptome were driven by variations in culture methods such as format, whereas experimental manipulations such as infection had modest effects. These results show that common variations in culture conditions can have large effects on intestinal organoids and should be accounted for when designing experiments and comparing results between laboratories. Our data constitute the largest RNA-seq dataset interrogating human intestinal epithelial organoids.

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