Conversion of amylase-secreting rat pancreatic AR42J cells to neuronlike cells by activin A

J Clin Invest. 1995 May;95(5):2304-14. doi: 10.1172/JCI117922.

Abstract

When AR42J cells, an amylase-secreting pancreatic exocrine cell line, were treated with activin A, cells extended neuritelike processes, and, concomitantly, amylase-containing vesicles disappeared. Immunofluorescence and immunoelectron microscopy revealed that these processes had neurite-specific cytoskeletal architectures: neurofilaments and microtubule bundles with cross-bridges of microtubule-associated protein 2. In addition to such morphological changes, activin-treated cells exhibited a marked increase in cytoplasmic free calcium concentration in response to depolarizing concentration of potassium. Moreover, activin-treated AR42J cells expressed mRNA for alpha 1 subunit of the neuroendocrine/beta cell-type voltage-dependent calcium channel. In naive AR42J cells, a sulfonylurea compound, tolbutamide, did not affect free calcium concentration, while it induced a marked elevation of free calcium in activin-treated cells. Single channel recording of the membrane patch revealed the existence of ATP-sensitive potassium channel in activin-treated cells. These results indicate that activin A converts amylase-secreting AR42J cells to neuronlike cells. Given that pancreatic endocrine cells possess neuronlike properties and express ATP-sensitive potassium channel as well as neuroendocrine/beta cell-type voltage-dependent calcium channel, activin treatment of AR42J cells may provide an in vitro model system to study the conversion of pancreatic exocrine cells to endocrine cells in islets.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activins
  • Adenosine Triphosphate / pharmacology
  • Amylases / biosynthesis*
  • Animals
  • Cell Differentiation / drug effects*
  • Cell Line
  • Cytoskeleton / drug effects
  • Cytoskeleton / physiology
  • Cytoskeleton / ultrastructure
  • Fluorescent Antibody Technique
  • Growth Substances / pharmacology
  • Inhibins / pharmacology*
  • Kinetics
  • Microscopy, Immunoelectron
  • Microtubule-Associated Proteins / analysis
  • Microtubule-Associated Proteins / biosynthesis
  • Neurites / drug effects
  • Neurites / physiology
  • Neurons / cytology*
  • Pancreas / cytology*
  • Pancreas / enzymology
  • Potassium Channels / drug effects
  • Potassium Channels / physiology
  • Rats
  • Tolbutamide / pharmacology
  • Tubulin / analysis

Substances

  • Growth Substances
  • Microtubule-Associated Proteins
  • Potassium Channels
  • Tubulin
  • Activins
  • Inhibins
  • Adenosine Triphosphate
  • Tolbutamide
  • Amylases