Exosomes derived from pancreatic cancer cells induce activation and profibrogenic activities in pancreatic stellate cells

Biochem Biophys Res Commun. 2018 Jan 1;495(1):71-77. doi: 10.1016/j.bbrc.2017.10.141. Epub 2017 Oct 28.

Abstract

Pancreatic cancer cells (PCCs) interact with pancreatic stellate cells (PSCs), which play a pivotal role in pancreatic fibrogenesis, to develop the cancer-conditioned tumor microenvironment. Exosomes are membrane-enclosed nanovesicles, and have been increasingly recognized as important mediators of cell-to-cell communications. The aim of this study was to clarify the effects of PCC-derived exosomes on cell functions in PSCs. Exosomes were isolated from the conditioned medium of Panc-1 and SUIT-2 PCCs. Human primary PSCs were treated with PCC-derived exosomes. PCC-derived exosomes stimulated the proliferation, migration, activation of ERK and Akt, the mRNA expression of α-smooth muscle actin (ACTA2) and fibrosis-related genes, and procollagen type I C-peptide production in PSCs. Ingenuity pathway analysis of the microarray data identified transforming growth factor β1 and tumor necrosis factor as top upstream regulators. PCCs increased the expression of miR-1246 and miR-1290, abundantly contained in PCC-derived exosomes, in PSCs. Overexpression of miR-1290 induced the expression of ACTA2 and fibrosis-related genes in PSCs. In conclusion, PCC-derived exosomes stimulate activation and profibrogenic activities in PSCs. Exosome-mediated interactions between PSCs and PCCs might play a role in the development of the tumor microenvironment.

Keywords: Fibrosis; Myofibroblast; Pancreatitis; Stroma; Tumor microenvironment; microRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / genetics
  • Actins / metabolism
  • Cell Communication
  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation
  • Cells, Cultured
  • Culture Media, Conditioned
  • Exosomes / metabolism*
  • Exosomes / pathology
  • Fibrosis
  • Gene Expression
  • Humans
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / metabolism*
  • Pancreatic Neoplasms / pathology*
  • Pancreatic Stellate Cells / metabolism*
  • Pancreatic Stellate Cells / pathology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / metabolism
  • Tumor Microenvironment

Substances

  • ACTA2 protein, human
  • Actins
  • Culture Media, Conditioned
  • MIRN1246 microRNA, human
  • MIRN1290 microRNA, human
  • MicroRNAs
  • RNA, Messenger
  • RNA, Neoplasm