Organization of the human intestine at single-cell resolution

John W. Hickey(Stanford Medicine), Winston R. Becker(Stanford Medicine), Stephanie Nevins(Stanford Medicine), Aaron M. Horning(Stanford Medicine), Almudena Espín Pérez(Stanford Medicine), Chenchen Zhu(Stanford Medicine), Bokai Zhu(Stanford Medicine), Bei Wei(Stanford Medicine), Roxanne Chiu(Stanford Medicine), Derek C. Chen(Stanford Medicine), Daniel L. Cotter(Stanford Medicine), Edward D. Esplin(Stanford Medicine), Annika K. Weimer(Stanford Medicine), Chiara Caraccio(Stanford Medicine), Vishal G. Venkataraaman(Stanford Medicine), Christian M. Schürch(Stanford Medicine), Sarah Black(Stanford Medicine), Maria Brbić(École Polytechnique Fédérale de Lausanne), Kaidi Cao(Stanford University), Shuxiao Chen(University of Pennsylvania), Weiruo Zhang(Stanford Medicine), Emma Monte(Stanford Medicine), Nancy R. Zhang(University of Pennsylvania), Zongming Ma(University of Pennsylvania), Jure Leskovec(Stanford University), Zhengyan Zhang(Washington University in St. Louis), Shin Lin(University of Washington), Teri A. Longacre(Stanford Medicine), Sylvia K. Plevritis(Stanford Medicine), Yiing Lin(Washington University in St. Louis), Garry P. Nolan(Stanford Medicine), William J. Greenleaf(Stanford Medicine), M Snyder(Stanford Medicine)
Nature
July 19, 2023
Cited by 303Open Access
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Abstract

Abstract The intestine is a complex organ that promotes digestion, extracts nutrients, participates in immune surveillance, maintains critical symbiotic relationships with microbiota and affects overall health 1 . The intesting has a length of over nine metres, along which there are differences in structure and function 2 . The localization of individual cell types, cell type development trajectories and detailed cell transcriptional programs probably drive these differences in function. Here, to better understand these differences, we evaluated the organization of single cells using multiplexed imaging and single-nucleus RNA and open chromatin assays across eight different intestinal sites from nine donors. Through systematic analyses, we find cell compositions that differ substantially across regions of the intestine and demonstrate the complexity of epithelial subtypes, and find that the same cell types are organized into distinct neighbourhoods and communities, highlighting distinct immunological niches that are present in the intestine. We also map gene regulatory differences in these cells that are suggestive of a regulatory differentiation cascade, and associate intestinal disease heritability with specific cell types. These results describe the complexity of the cell composition, regulation and organization for this organ, and serve as an important reference map for understanding human biology and disease.


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