Protective effects of intestinal trefoil factor (ITF) on gastric mucosal epithelium through activation of extracellular signal-regulated kinase 1/2 (ERK1/2)

Mol Cell Biochem. 2015 Jun;404(1-2):263-70. doi: 10.1007/s11010-015-2386-2. Epub 2015 Mar 17.

Abstract

The rapid repair of gastric mucosa is critical upon exposure to injurious agents. Intestinal trefoil factor (ITF) is a member of the trefoil factor family domain peptides, which play an important role in the cytoprotection of gastric epithelium. However, the underlying molecular mechanisms that are responsible for ITF-induced gastric epithelial repair remain unclear. In the present study, we demonstrate that ITF enhances the proliferation and migration of GES-1 gastric endothelial cells in a dose- and time-dependent manner through the activation of extracellular signal-regulated kinase 1/2 (ERK1/2). Furthermore, the ITF-mediated protection of GES-1 cells from a NS398 (nonsteroidal anti-inflammatory drug) was dependent on the ERK1/2 signaling pathway. Taken together, the results provide a mechanistic explanation for ITF-mediated protection of gastric epithelial mucosa cells, suggesting that activation of the ERK1/2 signaling pathway may provide a new therapeutic strategy for repairing gastric injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Cell Movement / genetics
  • Cell Proliferation / genetics
  • Epithelium / injuries
  • Epithelium / metabolism*
  • Gastric Mucosa / injuries
  • Gastric Mucosa / metabolism*
  • Gastric Mucosa / pathology
  • Humans
  • MAP Kinase Signaling System / genetics*
  • Nitrobenzenes / administration & dosage
  • Peptides / genetics
  • Peptides / metabolism*
  • Sulfonamides / administration & dosage
  • Trefoil Factor-2

Substances

  • Nitrobenzenes
  • Peptides
  • Sulfonamides
  • Trefoil Factor-2
  • N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide