Single-Cell Transcriptomic Analysis of the Mouse Pancreas: Characteristic Features of Pancreatic Ductal Cells in Chronic Pancreatitis

Genes (Basel). 2022 Jun 5;13(6):1015. doi: 10.3390/genes13061015.

Abstract

Chronic pancreatitis (CP) is a fibroinflammatory disorder of the pancreas. Our understanding of CP pathogenesis is partly limited by the incomplete characterization of pancreatic cell types. Here, we performed single-cell RNA sequencing on 3825 cells from the pancreas of one control mouse and mice with caerulein-induced CP. An analysis of the single-cell transcriptomes revealed 16 unique clusters and cell type-specific gene expression patterns in the mouse pancreas. Sub-clustering of the pancreatic mesenchymal cells from the control mouse revealed four clusters of cells with specific gene expression profiles (combinatorial expressions of Smoc2, Cxcl14, Tnfaip6, and Fn1). We observed that immune cells in the pancreas of the CP mice were abundant and diverse in cellular type. Compared to the control, 547 upregulated genes (including Mmp7, Ttr, Rgs5, Adh1, and Cldn2) and 257 downregulated genes were identified in ductal cells from the CP group. The elevated expression levels of MMP7 and TTR were further verified in the pancreatic ducts of CP patients. This study provides a preliminary description of the single-cell transcriptome profiles of mouse pancreata and accurately demonstrates the characteristics of pancreatic ductal cells in CP. The findings provide insight into novel disease-specific biomarkers and potential therapeutic targets of CP.

Keywords: caerulein; chronic pancreatitis; mesenchymal cells; mouse model; pancreatic ductal cells; single-cell analysis; transcriptome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Humans
  • Matrix Metalloproteinase 7 / genetics
  • Matrix Metalloproteinase 7 / metabolism
  • Mice
  • Pancreas / pathology
  • Pancreatic Ducts / metabolism
  • Pancreatic Ducts / pathology
  • Pancreatitis, Chronic* / genetics
  • Transcriptome* / genetics

Substances

  • Matrix Metalloproteinase 7

Grants and funding

This research was funded by the National Natural Science Foundation of China (Grant Nos. 82070661 (W.B.Z.), 81970560 (Z.L.), and 82170656 (L.W.)); the Scientific Innovation Program of Shanghai Municipal Education Committee (No. 201901070007E00052); the Top Young Program of Shanghai (W.B.Z.); and the “Clinical Technology Innovation Project Task (Contract)” of Shanghai Shenkang Hospital Development Center (No. SHDC2020CR2032B).