Connexin43 repression following epithelium-to-mesenchyme transition in embryonal carcinoma cells requires Snail1 transcription factor

Differentiation. 2007 Mar;75(3):208-18. doi: 10.1111/j.1432-0436.2006.00133.x.

Abstract

Embryonic stem (ES) cells and embryonal carcinoma (EC) cells express high amounts of functional connexin43 (Cx43). During mesoderm formation and subsequent cardiac differentiation, Cx43 is initially down-regulated but is up-regulated again as the emerging cardiomyocytes mature. In this study, we investigated the regulation of Cx43 expression during early phases of differentiation in F9 and P19 EC cells. We found a striking inverse correlation between the expression of Cx43 and that of the transcriptional repressor Snail1. No clear relationship was found with Smad-interacting-protein1 (SIP1), another transcription factor inducing epithelium-to-mesenchyme transition (EMT). Promoter-reporter assays indicated Cx43 repression at the promoter level by ectopically expressed Snail1. To establish whether the Cx43 down-regulation depends on endogenous Snail1, MES-1 cells, differentiated derivatives of P19 EC, were stably transfected by an siRNA construct silencing Snail1 expression. This resulted in a mesenchyme-to-epithelium transition, which was accompanied by increased levels of Cx43 mRNA and protein and enhanced metabolic and electrical coupling. We conclude that Snail1-mediated EMT results in a Cx43 repression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carcinoma, Embryonal
  • Cell Line, Tumor
  • Connexin 43 / genetics*
  • Connexin 43 / metabolism
  • Down-Regulation
  • Embryonic Stem Cells / cytology
  • Embryonic Stem Cells / metabolism*
  • Epithelium / metabolism*
  • Fluorescent Antibody Technique
  • Gene Silencing
  • Mesoderm / cytology
  • Mesoderm / metabolism*
  • Mice
  • Promoter Regions, Genetic
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / metabolism
  • Snail Family Transcription Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transfection

Substances

  • Connexin 43
  • RNA, Messenger
  • RNA, Small Interfering
  • Snai1 protein, mouse
  • Snail Family Transcription Factors
  • Transcription Factors