生物
克罗恩病
疾病
克罗恩病
计算生物学
遗传学
内科学
医学
作者
Rasa Elmentaite,Alexander Ross,Kenny Roberts,Kylie R. James,Daniel Ortmann,Tomás Gomes,Komal Nayak,Elizabeth Tuck,Sophie Pritchard,Omer Ali Bayraktar,Robert Heuschkel,Ludovic Vallier,Sarah A. Teichmann,Matthias Zilbauer
标识
DOI:10.1016/j.devcel.2020.11.010
摘要
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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