Cells of the human intestinal tract mapped across space and time

Rasa Elmentaite(Wellcome Sanger Institute), Natsuhiko Kumasaka(Wellcome Sanger Institute), Kenny Roberts(Wellcome Sanger Institute), Aaron Fleming(MRC Laboratory of Molecular Biology), Emma Dann(Wellcome Sanger Institute), Hamish W. King(Queen Mary University of London), Vitalii Kleshchevnikov(Wellcome Sanger Institute), Monika Dabrowska(Wellcome Sanger Institute), Sophie Pritchard(Wellcome Sanger Institute), Liam Bolt(Wellcome Sanger Institute), Sara F. Vieira(Wellcome Sanger Institute), Lira Mamanova(Wellcome Sanger Institute), Ni Huang(Wellcome Sanger Institute), Francesca Perrone(University of Cambridge), Issac Goh(Newcastle University), Steven Lisgo(Newcastle University), Matilda Katan(Institute of Structural and Molecular Biology), Steven Leonard(Wellcome Sanger Institute), Thomas R. W. Oliver(Cambridge University Hospitals NHS Foundation Trust), C. Elizabeth Hook(Cambridge University Hospitals NHS Foundation Trust), Komal Nayak(University of Cambridge), Lia S. Campos(Wellcome Sanger Institute), Cecilia Domínguez Conde(Wellcome Sanger Institute), Emily Stephenson(Newcastle University), Justin Engelbert(Newcastle University), Rachel A. Botting(Newcastle University), Krzysztof Polański(Wellcome Sanger Institute), Stijn van Dongen(Wellcome Sanger Institute), Minal Patel(Wellcome Sanger Institute), Michael D. Morgan(European Bioinformatics Institute), John C. Marioni(European Bioinformatics Institute), Omer Ali Bayraktar(Wellcome Sanger Institute), Kerstin B. Meyer(Wellcome Sanger Institute), Xiaoling He(Wellcome/MRC Cambridge Stem Cell Institute), Roger A. Barker(Wellcome/MRC Cambridge Stem Cell Institute), Holm H. Uhlig(John Radcliffe Hospital), Krishnaa T. Mahbubani(University of Cambridge), Kourosh Saeb‐Parsy(University of Cambridge), Matthias Zilbauer(Wellcome/MRC Cambridge Stem Cell Institute), Menna R. Clatworthy(MRC Laboratory of Molecular Biology), Muzlifah Haniffa(Wellcome Sanger Institute), Kylie R. James(Garvan Institute of Medical Research), Sarah A. Teichmann(University of Cambridge)
Nature
September 8, 2021
Cited by 690Open Access
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Abstract

The cellular landscape of the human intestinal tract is dynamic throughout life, developing in utero and changing in response to functional requirements and environmental exposures. Here, to comprehensively map cell lineages, we use single-cell RNA sequencing and antigen receptor analysis of almost half a million cells from up to 5 anatomical regions in the developing and up to 11 distinct anatomical regions in the healthy paediatric and adult human gut. This reveals the existence of transcriptionally distinct BEST4 epithelial cells throughout the human intestinal tract. Furthermore, we implicate IgG sensing as a function of intestinal tuft cells. We describe neural cell populations in the developing enteric nervous system, and predict cell-type-specific expression of genes associated with Hirschsprung's disease. Finally, using a systems approach, we identify key cell players that drive the formation of secondary lymphoid tissue in early human development. We show that these programs are adopted in inflammatory bowel disease to recruit and retain immune cells at the site of inflammation. This catalogue of intestinal cells will provide new insights into cellular programs in development, homeostasis and disease.


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