4.7 Article

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

期刊

DEVELOPMENTAL CELL
卷 55, 期 6, 页码 771-+

出版社

CELL PRESS
DOI: 10.1016/j.devcel.2020.11.010

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资金

  1. Wellcome Sanger Cytometry Core Facility
  2. Cellular Genetics Informatics team, Cellular Generation and Phenotyping (CGaP) core facility
  3. Core DNA Pipelines
  4. Horizon 2020 grant [668294]
  5. ERC Advanced Grant
  6. Cambridge University Hospitals National Institute for Health Research Biomedical Research Centre
  7. Wellcome Trust [WT206194]
  8. MRC
  9. European Research Council [646794]
  10. MRC New Investigator research grant [MR/T001917/1]
  11. Great Ormond Street Hospital Children's Charity, Sparks [V4519]
  12. European Research Council (ERC) [646794] Funding Source: European Research Council (ERC)
  13. EPSRC [TS/H001220/1] Funding Source: UKRI
  14. MRC [MR/T001917/1, MC_PC_17230, G0701448] Funding Source: UKRI

向作者/读者索取更多资源

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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