Regulation of HEF1 expression and phosphorylation by TGF-beta 1 and cell adhesion

J Biol Chem. 2002 Oct 18;277(42):39599-608. doi: 10.1074/jbc.M202263200. Epub 2002 Aug 19.

Abstract

Transforming growth factor-beta1 (TGF-beta1) is a multipotential cytokine, which regulates remodeling of tissue extracellular matrix during early tumorigenesis and wound healing. Human enhancer of filamentation-1 (HEF1), a multifunctional docking protein, is involved in integrin-based signaling, which affects cell motility, growth, and apoptosis. Our studies reveal that TGF-beta1 is a potent inducer of HEF1 gene transcription in human dermal fibroblasts. TGF-beta1 promoted HEF1 expression in a dose-dependent manner and resulted in a 16-fold increase in HEF1 protein level. TGF-beta1 had no effect on the stability of either HEF1 protein or mRNA. The TGF-beta1-induced HEF1 expression was independent of cell adhesion and resistant to cytoskeleton disruption. TGF-beta1 increased levels of both p105 and p115 HEF1 in adherent fibroblasts. Digestion with specific phosphatases indicated that the p115HEF1 resulted from serine/threonine phosphorylation of p105HEF1. The appearance of the p115HEF1 as well as tyrosine phosphorylation of p105HEF1 required cell adhesion and/or an organized cytoskeleton. An in vitro kinase assay indicated that p105HEF1 was a substrate for Src. PP1, a specific Src kinase inhibitor, was able to block adhesion-dependent tyrosine phosphorylation of p105HEF1. These findings suggest that TGF-beta1 regulates HEF1 gene expression and that HEF1 phosphorylation is dependent on cell adhesion and Src kinase activity.

Publication types

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

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Apoptosis
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology
  • Catalysis
  • Cell Adhesion
  • Cell Division
  • Cell Line
  • Cells, Cultured
  • Cytochalasin D / pharmacology
  • Cytoskeleton / metabolism
  • Dactinomycin / pharmacology
  • Dose-Response Relationship, Drug
  • Fibroblasts / metabolism
  • Gene Expression Regulation*
  • Humans
  • Immunoblotting
  • Phosphoproteins / genetics*
  • Phosphoproteins / metabolism*
  • Phosphorylation
  • Precipitin Tests
  • Protein Binding
  • Protein Synthesis Inhibitors / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Serine / metabolism
  • Signal Transduction
  • Substrate Specificity
  • Thiazoles / pharmacology
  • Thiazolidines
  • Threonine / metabolism
  • Time Factors
  • Transcription, Genetic
  • Transforming Growth Factor beta / metabolism*
  • Transforming Growth Factor beta1
  • Tyrosine / metabolism
  • Up-Regulation

Substances

  • Adaptor Proteins, Signal Transducing
  • Bridged Bicyclo Compounds, Heterocyclic
  • NEDD9 protein, human
  • Phosphoproteins
  • Protein Synthesis Inhibitors
  • TGFB1 protein, human
  • Thiazoles
  • Thiazolidines
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • Dactinomycin
  • Cytochalasin D
  • Threonine
  • Tyrosine
  • Serine
  • latrunculin A