single-cell RNA sequencing of healthy control, ulcerative colitis, and primary sclerosing cholangitis concomitant with ulcerative colitis colonic mucosa
Download from source ↗Dataset overview
Primary sclerosing cholangitis displays distinct colonic mucosa topography yet a shared mast cell state with ulcerative colitis.
Abstract
Primary sclerosing cholangitis (PSC) is a chronic, progressing cholestatic disease that often co-occurs with inflammatory bowel disease (PSC-IBD). PSC-IBD affecting the colon (PSC-ulcerative colitis or PSC-UC) resembles clinical UC, but is characterised by less severe disease flares, right-colon predominance, and a greater lifetime risk of colorectal cancer than UC alone. To elucidate differences in the underlying biology between PSC-UC and UC, here we combine single-cell mRNA and antigen receptor sequencing, 16S ribosomal RNA gene analysis and spatial transcriptomics on biopsies from four colon regions of patients with PSC-UC and UC during endoscopic remission or at the time of relapse. We show that the PSC-UC colon, compared to healthy control (HC) or UC colon, harbours distinct and region-specific mucosal-adherent microbial communities and an enrichment of activated CD8 T and γδ T cells at the right colon, even in the absence of histological inflammation. By contrast, a TMEM176B<sup>+</sup> mast cell population that may be pro-tumourigenic is enriched in the colon during disease relapse in both PSC-UC and UC colon. These results highlight that the PSC-UC and UC colonic mucosa are fundamentally different while sharing similar cell programmes during active disease. Our data thus provide insights to guide tailored clinical management and precision therapies.
Study facts
- Organism
- Homo sapiens
- Platform
- 10x Genomics
- Age group
- adult
- Disease groups
- —
- Anatomical sites
- ascending colon, descending colon, rectum, transverse colon
Data availability
- Processed matrix
File types
H5AD
Files and samples
Strengths & limitations for reuse
Strengths
- Processed matrices are advertised
- Cell metadata are advertised
- Participant counts are documented
Limitations
- Not documented: raw counts are advertised
Extraction evidence & provenance
Each extracted field is shown with the source excerpt and location used to resolve it.
Assay
| Field | Value | Evidence |
|---|---|---|
assay.assay_type |
10x 5' v2 from source |
assay=10x 5' v2 Section |
assay.library_chemistry |
10x 5' v2 and 10x 5' v3 |
"assay": [{"label": "10x 5' v2", "ontology_term_id": "EFO:0009900"}, {"label": "10x 5' v3", "ontology_term_id": "EFO:0022605"}] Section |
assay.platform |
10x Genomics inferred |
"assay": [{"label": "10x 5' v2" Section |
assay.sequencing_type |
scrna_seq from source |
sequencing_type=scrna_seq Section |
Cohort
| Field | Value | Evidence |
|---|---|---|
cohort.age_group |
adult inferred |
"development_stage": [{"label": "21-year-old stage" Section |
cohort.disease_activity_metadata_available |
True |
patients with PSC-UC and UC during endoscopic remission or at the time of relapse Section |
cohort.total_participants |
22 inferred |
"donor_id": ["PSC-1", "PSC-2", "PSC-3", "UC-1", "UC-2", "UC-3", "UC-4", "PSC-4", "UC-7", "PSC-5", "UC-8", "PSC-6", "UC-10", "HC-1", "PSC-7", "UC-9", "411c", "414c", "417c", "432c", "440c", "HC-2"] Section |
Data_Assets
| Field | Value | Evidence |
|---|---|---|
data_assets.cell_metadata |
True from source |
CELLxGENE dataset exposes cell metadata Section |
data_assets.open_access |
True from source |
public CELLxGENE dataset Section |
data_assets.participant_metadata |
True |
"donor_id": ["PSC-1", "PSC-2", "PSC-3", "UC-1", "UC-2", "UC-3", "UC-4", "PSC-4", "UC-7", "PSC-5", "UC-8", "PSC-6", "UC-10", "HC-1", "PSC-7", "UC-9", "411c", "414c", "417c", "432c", "440c", "HC-2"] Section |
data_assets.processed_matrix |
True from source |
CELLxGENE dataset exposes H5AD Section |
Specimens
| Field | Value | Evidence |
|---|---|---|
specimens.anatomical_sites |
['ascending colon', 'descending colon', 'rectum', 'transverse colon'] from source |
tissues=ascending colon, descending colon, rectum, transverse colon Section |
specimens.inflamed_status_available |
True |
even in the absence of histological inflammation Section |
specimens.number_of_cells |
320979 from source |
cell_count=320979 Section |
specimens.specimen_type |
biopsy |
single-cell mRNA and antigen receptor sequencing ... on biopsies from four colon regions Section |