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. Author manuscript; available in PMC: 2023 Feb 1.
Published in final edited form as: Sci Immunol. 2022 May 13;7(71):eabl6543. doi: 10.1126/sciimmunol.abl6543

Figure 2. IL-13 and IL-22 induce different subsets of goblet cell genes.

Figure 2

A, Heatmap of NES values from GSEA analysis of gene sets representing different cell types compared to RNAseq data from organoids treated for 24 hours with cytokines, see supplementary file 1 for gene sets. B, Distribution of how the goblet cell gene set from plate based scRNAseq from Haber et al is changed upon 24 hour IL-13 and IL-22 treatment in organoids. Up is defined as log2fc>0.5 and p-adj<0.05. C, Gene expression from intestinal organoids treated for 24 hours with indicated cytokine. Statistics calculated with DESeq2, details in methods. D, E, Confocal staining of MUC2 and UEA1 2 days after splitting (D) and RELMĪ² and UEA1 at 3 days after splitting (E) in small intestinal organoids. Representative images of three mice. 5 ng/mL of IL-22 and 10 ng/mL of IL-13 was used. F,G, Quantification of images acquired as in D and E. Pixels are defined as positive above a set threshold. Each circle represents one organoid and statistics calculated with unpaired two tailed T-test. H, See C. I, GSEA of IL-22 specific goblet cell genes from B compared to RNAseq data from organoids stimulated with IL-22 for 1h and 4h. All images are projections of Z-stacks.