Single-Cell Sequencing of Developing Human Gut Reveals Transcriptional Links to Childhood Crohn’s Disease

Rasa Elmentaite(Wellcome Sanger Institute), Alexander Ross(Wellcome/MRC Cambridge Stem Cell Institute), Kenny Roberts(Wellcome Sanger Institute), Kylie R. James(Wellcome Sanger Institute), Daniel Ortmann(Wellcome/MRC Cambridge Stem Cell Institute), Tomás Gomes(Wellcome Sanger Institute), Komal Nayak(University of Cambridge), Elizabeth Tuck(Wellcome Sanger Institute), Sophie Pritchard(Wellcome Sanger Institute), Omer Ali Bayraktar(Wellcome Sanger Institute), Robert Heuschkel(Cambridge University Hospitals NHS Foundation Trust), Ludovic Vallier(Wellcome/MRC Cambridge Stem Cell Institute), Sarah A. Teichmann(European Bioinformatics Institute), Matthias Zilbauer(Wellcome/MRC Cambridge Stem Cell Institute)
Developmental Cell
December 1, 2020
Cited by 332Open Access
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Abstract

Human gut development requires the orchestrated interaction of differentiating cell types. Here, we generate an in-depth single-cell map of the developing human intestine at 6-10 weeks post-conception. Our analysis reveals the transcriptional profile of cycling epithelial precursor cells; distinct from LGR5-expressing cells. We propose that these cells may contribute to differentiated cell subsets via the generation of LGR5-expressing stem cells and receive signals from surrounding mesenchymal cells. Furthermore, we draw parallels between the transcriptomes of ex vivo tissues and in vitro fetal organoids, revealing the maturation of organoid cultures in a dish. Lastly, we compare scRNA-seq profiles from pediatric Crohn's disease epithelium alongside matched healthy controls to reveal disease-associated changes in the epithelial composition. Contrasting these with the fetal profiles reveals the re-activation of fetal transcription factors in Crohn's disease. Our study provides a resource available at www.gutcellatlas.org, and underscores the importance of unraveling fetal development in understanding disease.


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