Autocrine stimulation of human pancreatic duct-like development by soluble isoforms of epimorphin in vitro

J Cell Biol. 2001 Mar 5;152(5):911-22. doi: 10.1083/jcb.152.5.911.

Abstract

Epimorphin was recently described as a mesenchymal factor modulating morphogenesis of murine mammary ducts, skin, liver, and lung in vitro. In this study epimorphin was analyzed in a human, pancreatic adenocarcinoma cell line (A818-6) which develops single layer epithelial hollow spheres resembling normal pancreatic ductal structures in vitro. Soluble 34- and 31-kD isoforms of epimorphin were found in the culture supernatant of A818-6 cells. In lysates of A818-6 cells we detected the 34-and 31-kD isoforms and the dimers, and in lysates of fibroblasts the 150-kD tetramers of epimorphin additionally. A neutralizing monoclonal antibody against epimorphin (MC-1) efficiently blocked the development of hollow sphere structures from A818-6 cells. Coculture of A818-6 cells with fibroblasts stimulated the development of hollow sphere structures in general and increased differentiation in 5-6-d-old hollow spheres. A818-6 hollow sphere development in the presence of fibroblasts was also blocked by MC-1. In this novel system for human duct-like differentiation of pancreatic epithelial cells, we provide evidence for an autocrine and paracrine function of epimorphin as a major mediator for morphogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma
  • Aged
  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / pharmacology
  • Autocrine Communication* / drug effects
  • Biomarkers / analysis
  • Cell Adhesion
  • Cell Aggregation / drug effects
  • Cell Differentiation
  • Cell Division / drug effects
  • Cell Line
  • Coculture Techniques
  • Culture Media, Conditioned / metabolism
  • Dimerization
  • Female
  • Fibroblasts
  • Fluorescent Antibody Technique
  • Growth Substances / pharmacology
  • Humans
  • Membrane Glycoproteins / chemistry
  • Membrane Glycoproteins / immunology
  • Membrane Glycoproteins / metabolism*
  • Morphogenesis / drug effects
  • Pancreatic Ducts / cytology*
  • Pancreatic Ducts / drug effects
  • Pancreatic Ducts / metabolism
  • Pancreatic Ducts / ultrastructure
  • Protein Isoforms / chemistry
  • Protein Isoforms / immunology
  • Protein Isoforms / metabolism
  • Solubility
  • Syntaxin 1
  • Tumor Cells, Cultured

Substances

  • Antibodies, Monoclonal
  • Biomarkers
  • Culture Media, Conditioned
  • Growth Substances
  • Membrane Glycoproteins
  • Protein Isoforms
  • STX2 protein, human
  • Syntaxin 1