TGF-beta induces connexin43 gene expression in normal murine mammary gland epithelial cells via activation of p38 and PI3K/AKT signaling pathways

J Cell Physiol. 2008 Dec;217(3):759-68. doi: 10.1002/jcp.21551.

Abstract

One of the shared physiological roles between TGF-beta and connexin family members is to inhibit epithelial cell cycle progression and consequently, to provide protection against malignant transformation. Herein, we demonstrated that TGF-beta1 induces the expression of connexin43 (Cx43) in normal murine mammary gland (NMuMG) cell lines at the protein and mRNA levels, and transcriptionally. Using overexpression of a truncated dominant-negative form of Cx43, we determined that the modulation of gap junctional communication by TGF-beta1 plays a key role in the control of NMuMG cells proliferation by TGF-beta1. In addition, using overexpression of truncated dominant-negative forms of either Smad2 or Smad3, and MDA-MB-468 human breast carcinoma cells deficient for Smad4, we determined that the Smad cascade is not implicated in TGF-beta1 effect on Cx43 expression. Using specific pharmacologic inhibitors for JNK, ERK, p38, and PI3K/AKT signaling pathways, we demonstrated the cooperative role of p38 and PI3K/AKT signaling in TGF-beta1-induced Cx43 expression and gap junctional communication. Furthermore, transfection of a c-jun antisense expression vector significantly prevented TGF-beta1-induced Cx43 gene expression demonstrating the involvement of c-Jun/AP-1 pathway together with p38 and PI3K/AKT pathways in mediating TGF-beta1-induced Cx43 gene expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Communication / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Connexin 43 / genetics*
  • Enzyme Activation / drug effects
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Epithelial Cells / enzymology*
  • Female
  • Gap Junctions / drug effects
  • Gap Junctions / enzymology
  • Humans
  • Mammary Glands, Animal / cytology*
  • Mammary Glands, Animal / enzymology
  • Mice
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Promoter Regions, Genetic / genetics
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Proto-Oncogene Proteins c-jun / metabolism
  • Signal Transduction / drug effects
  • Smad Proteins / metabolism
  • Transcription, Genetic / drug effects
  • Transcriptional Activation / drug effects
  • Transforming Growth Factor beta1 / pharmacology*
  • Xenopus
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Connexin 43
  • Proto-Oncogene Proteins c-jun
  • Smad Proteins
  • Transforming Growth Factor beta1
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt
  • p38 Mitogen-Activated Protein Kinases