Organization of the human intestine at single-cell resolution

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Updated August 26, 2025

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. The intesting has a length of over nine metres, along which there are differences in structure and function. 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.

Garry P NolanStanford School of Medicinegnolan@stanford.edu
William J GreenleafStanford School of Medicinewjg@stanford.edu
Michael SnyderStanford School of Medicinempsnyder@stanford.edu
John W Hickey1
Winston R Becker1
Stephanie A Nevins1
Aaron Horning1
Almudena Espin Perez1
Chenchen Zhu1
Bokai Zhu1
Bei Wei1
Roxanne Chiu1
Derek C Chen1
Daniel L Cotter1
Edward D Esplin1
Annika K Weimer1
Chiara Caraccio1
Vishal Venkataraaman1
Christian M Schürch1
Sarah Black1
Maria Brbić2
Kaidi Cao2
Shuxiao Chen3
Weiruo Zhang1
Emma Monte1
Nancy R Zhang3
Zongming Ma3
Jure Leskovec2
Zhengyan Zhang4
Shin Lin5
Teri Longacre1
Sylvia K Plevritis1
Yiing Lin4
Garry P Nolan1
William J Greenleaf1
Michael Snyder1
1Stanford School of Medicine
2Stanford University
3University of Pennsylvania
4Washington University
5University of Washington
Ida Zucchi

To reference this project, please use the following link:

https://explore.data.humancellatlas.org/projects/16241d82-3119-4bdd-bba5-5097c0591ba0

Supplementary links are provided by contributors and represent items such as additional data which can’t be hosted here; code that was used to analyze this data; or tools and visualizations associated with this specific dataset.

1.https://doi.org/10.35079/HBM692.JRZB.3562.https://doi.org/10.5061/dryad.0zpc8672f3.https://doi.org/10.5061/dryad.8pk0p2ns8
None

Atlas

GutGut v1.0

Analysis Portals

None

Project Label

IntestineOrganizationHickey

Species

Homo sapiens

Sample Type

specimens

Anatomical Entity

4 anatomical entities

Organ Part

7 organ parts

Selected Cell Types

Unspecified

Disease Status (Specimen)

normal

Disease Status (Donor)

3 disease statuses

Development Stage

human adult stage

Library Construction Method

3 library construction methods

Nucleic Acid Source

single nucleus

Paired End

false, true

Analysis Protocol

ATAC_tracks, cell_UMAP, processed_matrix_generation_RNA, raw_matrix_generation_ATAC, raw_matrix_generation_RNA, raw_matrix_generation_multiome

File Format

6 file formats

Cell Count Estimate

Unspecified

Donor Count

9
bed.gz12 file(s)mtx.gz87 file(s)rds.gz8 file(s)tsv.gz254 file(s)tsv.gz.tbi72 file(s)xlsx1 file(s)
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