Adipose Stem Cell Therapy Mitigates Chronic Pancreatitis via Differentiation into Acinar-like Cells in Mice

Mol Ther. 2017 Nov 1;25(11):2490-2501. doi: 10.1016/j.ymthe.2017.06.016. Epub 2017 Aug 4.

Abstract

The objective of this study was to assess the capacity of adipose-derived mesenchymal stem cells (ASCs) to mitigate disease progression in an experimental chronic pancreatitis mouse model. Chronic pancreatitis (CP) was induced in C57BL/6 mice by repeated ethanol and cerulein injection, and mice were then infused with 4 × 105 or 1 × 106 GFP+ ASCs. Pancreas morphology, fibrosis, inflammation, and presence of GFP+ ASCs in pancreases were assessed 2 weeks after treatment. We found that ASC infusion attenuated pancreatic damage, preserved pancreas morphology, and reduced pancreatic fibrosis and cell death. GFP+ ASCs migrated to pancreas and differentiated into amylase+ cells. In further confirmation of the plasticity of ASCs, ASCs co-cultured with acinar cells in a Transwell system differentiated into amylase+ cells with increased expression of acinar cell-specific genes including amylase and chymoB1. Furthermore, culture of acinar or pancreatic stellate cell lines in ASC-conditioned medium attenuated ethanol and cerulein-induced pro-inflammatory cytokine production in vitro. Our data show that a single intravenous injection of ASCs ameliorated CP progression, likely by directly differentiating into acinar-like cells and by suppressing inflammation, fibrosis, and pancreatic tissue damage. These results suggest that ASC cell therapy has the potential to be a valuable treatment for patients with pancreatitis.

Keywords: acinar cells; adipose stem cell therapy; differentiation; ethanol and cerulean-induced chronic pancreatitis mouse model; fibrosis; inflammation; mesenchymal stem cells.

MeSH terms

  • Acinar Cells / cytology
  • Acinar Cells / drug effects
  • Acinar Cells / metabolism
  • Adipose Tissue / cytology*
  • Adipose Tissue / metabolism
  • Amylases / genetics
  • Amylases / metabolism
  • Animals
  • Cell Differentiation
  • Cell Movement
  • Cell- and Tissue-Based Therapy / methods*
  • Ceruletide / administration & dosage
  • Coculture Techniques
  • Culture Media, Conditioned / pharmacology
  • Ethanol / administration & dosage
  • Gene Expression
  • Genes, Reporter
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Humans
  • Interleukin-6 / antagonists & inhibitors
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism
  • Male
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Pancreas / metabolism
  • Pancreas / pathology
  • Pancreatitis, Chronic / chemically induced
  • Pancreatitis, Chronic / genetics
  • Pancreatitis, Chronic / pathology
  • Pancreatitis, Chronic / therapy*
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Culture Media, Conditioned
  • Interleukin-6
  • Tumor Necrosis Factor-alpha
  • interleukin-6, mouse
  • Green Fluorescent Proteins
  • Ethanol
  • Ceruletide
  • Amylases