A human stomach cell type transcriptome atlas Show others and affiliations
2024 (English) In: BMC Biology, E-ISSN 1741-7007, Vol. 22, no 1, article id 36Article in journal (Refereed) Published
Abstract [en]
Background
The identification of cell type-specific genes and their modification under different conditions is central to our understanding of human health and disease. The stomach, a hollow organ in the upper gastrointestinal tract, provides an acidic environment that contributes to microbial defence and facilitates the activity of secreted digestive enzymes to process food and nutrients into chyme. In contrast to other sections of the gastrointestinal tract, detailed descriptions of cell type gene enrichment profiles in the stomach are absent from the major single-cell sequencing-based atlases.
Results
Here, we use an integrative correlation analysis method to predict human stomach cell type transcriptome signatures using unfractionated stomach RNAseq data from 359 individuals. We profile parietal, chief, gastric mucous, gastric enteroendocrine, mitotic, endothelial, fibroblast, macrophage, neutrophil, T-cell, and plasma cells, identifying over 1600 cell type-enriched genes.
Conclusions
We uncover the cell type expression profile of several non-coding genes strongly associated with the progression of gastric cancer and, using a sex-based subset analysis, uncover a panel of male-only chief cell-enriched genes. This study provides a roadmap to further understand human stomach biology.
Place, publisher, year, edition, pages BioMed Central (BMC), 2024. Vol. 22, no 1, article id 36
Keywords [en]
Cell profiling, Gene enrichment, Bulk RNAseq, Stomach
National Category
Cell and Molecular Biology
Identifiers URN: urn:nbn:se:uu:diva-524333 DOI: 10.1186/s12915-024-01812-5 ISI: 001162444800002 PubMedID: 38355543 OAI: oai:DiVA.org:uu-524333 DiVA, id: diva2:1842032
Funder Knut and Alice Wallenberg Foundation Swedish Heart Lung Foundation, 20170759 Swedish Heart Lung Foundation, 20170537 Swedish Heart Lung Foundation, 20200544 Swedish Research Council, 2019-01493 Region Stockholm, 2017–0842 2024-03-012024-03-012024-03-01 Bibliographically approved