p38 MAPK is involved in activin A- and hepatocyte growth factor-mediated expression of pro-endocrine gene neurogenin 3 in AR42J-B13 cells

J Biol Chem. 2003 Jun 13;278(24):21693-700. doi: 10.1074/jbc.M302684200. Epub 2003 Apr 1.

Abstract

Neurogenin3 (ngn3) is a transcription factor that is essential for the differentiation of pancreatic endocrine cells. To investigate the signaling pathway that regulates ngn3 expression, we used AR42J-B13 cells as a model of the differentiation of pancreatic islets. In these cells, treatment with activin A and hepatocyte growth factor (HGF) induced the expression of ngn3. Reporter gene analysis using human ngn3 gene (NEUROG3) promoter fragments of various lengths identified the region between -402 and -327 bp of NEUROG3 as an activin A- and HGF-responsive DNA sequence. This DNA sequence normally functions as a repressor in AR42J-B13 cells, but treatment with activin A and HGF negates the repressor activity. Interestingly, function of the activin A- and HGF-responsive sequence was not influenced by the overexpression of the Smad inhibitory factor, Smad7. Instead, activin A and HGF activation was inhibited by overexpression of a dominant-negative mutant of transforming growth factor-beta-activated kinase 1 (TAK1), or mitogen-activated protein kinase kinase 3 (MKK3), or by treatment with a p38 MAPK-specific inhibitor, SB203580. Activin A and HGF function through the TAK1-MKK3-p38 MAPK pathway to relieve transcription repressors located between -402 and -326 bp on the NEUROG3 promoter, and consequently activate ngn3 expression and endocrine differentiation of AR42J-B13 cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activins / metabolism*
  • Basic Helix-Loop-Helix Transcription Factors
  • Cell Differentiation
  • Cell Line
  • DNA / metabolism
  • Endocrine Glands / cytology
  • Enzyme Inhibitors / pharmacology
  • Genes, Dominant
  • Genes, Reporter
  • Hepatocyte Growth Factor / metabolism*
  • Humans
  • Inhibin-beta Subunits / metabolism*
  • Islets of Langerhans / cytology
  • Luciferases / metabolism
  • Mitogen-Activated Protein Kinases / metabolism*
  • Mutation
  • Nerve Tissue Proteins / metabolism*
  • Signal Transduction
  • Time Factors
  • Transcription, Genetic
  • Transcriptional Activation
  • Transfection
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Enzyme Inhibitors
  • NEUROG3 protein, human
  • Nerve Tissue Proteins
  • activin A
  • Activins
  • Hepatocyte Growth Factor
  • DNA
  • Inhibin-beta Subunits
  • Luciferases
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases