Format

Send to

Choose Destination
Sci Rep. 2019 Mar 14;9(1):4536. doi: 10.1038/s41598-019-40809-x.

Single-cell transcriptome analysis identifies distinct cell types and niche signaling in a primary gastric organoid model.

Author information

1
Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.
2
Stanford Genome Technology Center, Stanford University School of Medicine, Stanford, CA, USA.
3
Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA. genomics_ji@stanford.edu.
4
Stanford Genome Technology Center, Stanford University School of Medicine, Stanford, CA, USA. genomics_ji@stanford.edu.

Abstract

The diverse cellular milieu of the gastric tissue microenvironment plays a critical role in normal tissue homeostasis and tumor development. However, few cell culture model can recapitulate the tissue microenvironment and intercellular signaling in vitro. We used a primary tissue culture system to generate a murine p53 null gastric tissue model containing both epithelium and mesenchymal stroma. To characterize the microenvironment and niche signaling, we used single cell RNA sequencing (scRNA-Seq) to determine the transcriptomes of 4,391 individual cells. Based on specific markers, we identified epithelial cells, fibroblasts and macrophages in initial tissue explants during organoid formation. The majority of macrophages were polarized towards wound healing and tumor promotion M2-type. During the course of time, the organoids maintained both epithelial and fibroblast lineages with the features of immature mouse gastric stomach. We detected a subset of cells in both lineages expressing Lgr5, one of the stem cell markers. We examined the lineage-specific Wnt signaling activation, and identified that Rspo3 was specifically expressed in the fibroblast lineage, providing an endogenous source of the R-spondin to activate Wnt signaling. Our studies demonstrate that this primary tissue culture system enables one to study gastric tissue niche signaling and immune response in vitro.

Supplemental Content

Full text links

Icon for Nature Publishing Group Icon for PubMed Central
Loading ...
Support Center