Smad4 mediates activation of mitogen-activated protein kinases by TGF-beta in pancreatic acinar cells

Am J Physiol Cell Physiol. 2001 Jul;281(1):C311-9. doi: 10.1152/ajpcell.2001.281.1.C311.

Abstract

Transforming growth factor-beta (TGF-beta) inhibits pancreatic acinar cell growth. In many cell types, TGF-beta mediates its growth inhibitory effects by activation of Smad proteins. Recently, it has been reported that Smad proteins may interact with the mitogen-activated protein (MAP) kinase signaling pathways. In this study, we report on the interactions between the TGF-beta and MAP kinase signaling pathways in isolated rat pancreatic acinar cells. TGF-beta activated the MAP kinases extracellular signal-related kinases (ERKs) and p38 in pancreatic acinar cells, but had no effect on c-jun NH2-terminal kinase activity. Activation of MAP kinase by TGF-beta was maximal 4 h after treatment. The ability of TGF-beta to activate ERKs was concentration dependent and dependent on protein synthesis. TGF-beta's stimulation of ERK activation was blocked by PD-98059, an inhibitor of MAP kinase kinase 1, and by adenoviral transfer of dominant negative RasN17. Furthermore, adenoviral-mediated expression of dominant negative Smad4 blocked the ability of TGF-beta to activate acinar cell MAP kinase, demonstrating that this activation is downstream of Smads. The biological relevance of ERK activation by TGF-beta was indicated by demonstrating that inhibition of ERK signaling by PD-98059 blocked the ability of TGF-beta to activate the transcription factor activator protein-1. These studies provide new insight into the signaling mechanisms by which TGF-beta mediates biological actions in pancreatic acinar cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenoviridae / genetics
  • Animals
  • Cholecystokinin / pharmacology
  • Cycloheximide / pharmacology
  • DNA-Binding Proteins / metabolism*
  • Enzyme Activation
  • Enzyme Inhibitors / pharmacology
  • Flavonoids / pharmacology
  • Genes, Reporter
  • Immunoblotting
  • In Vitro Techniques
  • MAP Kinase Kinase 1
  • MAP Kinase Signaling System*
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinases / metabolism*
  • Pancreas / cytology
  • Pancreas / enzymology
  • Pancreas / metabolism*
  • Protein Binding
  • Protein Serine-Threonine Kinases / metabolism
  • Protein Synthesis Inhibitors / pharmacology
  • Rats
  • Rats, Wistar
  • Smad4 Protein
  • Trans-Activators / metabolism*
  • Transcription Factor AP-1 / metabolism
  • Transforming Growth Factor beta / metabolism*
  • p38 Mitogen-Activated Protein Kinases
  • ras Proteins / genetics
  • ras Proteins / metabolism

Substances

  • DNA-Binding Proteins
  • Enzyme Inhibitors
  • Flavonoids
  • Protein Synthesis Inhibitors
  • Smad4 Protein
  • Smad4 protein, rat
  • Trans-Activators
  • Transcription Factor AP-1
  • Transforming Growth Factor beta
  • Cholecystokinin
  • Cycloheximide
  • Protein Serine-Threonine Kinases
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 1
  • MAP2K1 protein, human
  • Mitogen-Activated Protein Kinase Kinases
  • ras Proteins
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one