HCA Data Explorer

Cells of the human intestinal tract mapped across space and time

Access Granted
Updated August 30, 2022

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. To comprehensively map cell lineages in the healthy developing, pediatric and adult human gut from ten distinct anatomical regions, as well as draining lymph nodes, we used single cell RNA-seq and VDJ analysis of roughly one third of a million cells. This reveals the presence of BEST4+ absorptive cells throughout the human intestinal tract, demonstrating the existence of this cell type beyond the colon for the first time. Furthermore, we implicate IgG sensing as a novel function of intestinal tuft cells, and link these cells to the pathogenesis of inflammatory bowel disease. We define novel glial and neuronal cell populations in the developing enteric nervous system, and predict cell-type specific expression of Hirschsprung’s disease-associated genes. Finally, using a systems approach, we identify key cell players across multiple cell lineages driving secondary lymphoid tissue formation 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. These data provide an unprecedented catalogue of intestinal cells, and new insights into cellular programs in development, homeostasis and disease.

Kylie R JamesWellcome Sanger Institute, Wellcome Genome Campuskj7@sanger.ac.uk
Sarah A  TeichmannWellcome Sanger Institute, Wellcome Genome Campusst9@sanger.ac.uk
Rasa Elmentaite1
Natsuhiko Kumasaka1
Hamish W King2
Kenny Roberts1
Monika Dabrowska1
Sophie Pritchard1
Liam Bolt1
Sara F Vieira1
Lira Mamanova1
Ni Huang1
Isaac E Goh Kai’En3
Emily Stephenson3
Justin Engelbert3
Rachel A Botting3
A Fleming1
Emma Dann1
Steven N Lisgo3
Matilda Katan4
Steven Leonard1
Thomas RW Oliver1
C E Hook5
Komal Nayak6
Francesca Perrone6
Lia S Campos1
Cecilia Dominguez-Conde1
Krzysztof Polanski1
Stijn van Dongen1
Minal Patel1
Michael D Morgan7
John C Marioni1
Omer A Bayraktar1
Kerstin B Meyer1
Matthias Zilbauer8
Holm Uhlig9
Menna R Clatworthy1
Krishnaa T Mahbubani10
Kourosh Saeb Parsy10
Muzlifah Haniffa3
Kylie R James1
Sarah A  Teichmann1
1Wellcome Sanger Institute, Wellcome Genome Campus
2Centre for Immunobiology, Queen Mary University of London
3Biosciences Institute, Faculty of Medical Sciences, Newcastle University
4Structural and Molecular Biology, University College London
5Department of Histopathology, Cambridge University Hospitals NHS Foundation Trust
6Department of Paediatrics, University of Cambridge
7EMBL-EBI
8Wellcome Trust - MRC Cambridge Stem Cell Institute
9Translational Gastroenterology Unit, John Radcliffe Hospital
10Department of Surgery, University of Cambridge and NIHR Cambridge Biomedical Research Centre
Wei Kheng Teh

To reference this project, please use the following link:

https://explore.data.humancellatlas.org/projects/fde199d2-a841-4ed1-aa65-b9e0af8969b1
None
Array Express Accessions:
E-MTAB-9543, E-MTAB-9536, E-MTAB-9532, E-MTAB-9533, E-MTAB-10386

Atlas

None

Analysis Portals

CZ CELLxGENECZ CELLxGENE
UCSC Cell BrowserUCSC Cell Browser

Project Label

IntestinalSpaceTime

Species

Homo sapiens

Sample Type

specimens

Anatomical Entity

4 anatomical entities

Organ Part

15 organ parts

Selected Cell Types

8 cell types

Disease Status (Specimen)

type 2 diabetes mellitus

Disease Status (Donor)

2 disease statuses

Development Stage

2 development stages

Library Construction Method

2 library construction methods

Nucleic Acid Source

single nucleus

Paired End

false

Analysis Protocol

Matrixanalysis, Processedmatrixgeneration, Visiumanalysis

File Format

5 file formats

Cell Count Estimate

428.0k

Donor Count

12
fastq.gz540 file(s)h5ad1 file(s)ndpi3 file(s)txt1 file(s)xlsx1 file(s)