Induction of Oct-3/4 expression in somatic cells by gap junction-mediated cAMP signaling from blastomeres

Eur J Cell Biol. 2002 Nov;81(11):585-91. doi: 10.1078/0171-9335-00286.

Abstract

We report the induction of embryonic gene expression in epithelial HC-11 cells upon communication with blastomeres in compacting mouse embryos. In contrast to NIH3T3 fibroblasts, HC-11 epithelial cells form gap junctions with blastomeres after injection into cleavage-stage embryos, as shown by targeting of phosphorylated connexin43 (pCx43) to areas of cell-to-blastomere contact and dye coupling. This was accompanied by expression of the embrvo-specific transcription factor, Oct-3/4, in the HC-11 cells. Dye coupling and Oct-3/4 expression were abolished with heptanol and 18beta- glycyrrhetinic acid, two gap junction blockers. Oleamide, which blocks gap junction-mediated communication but not electrical conductance, also inhibited Oct-3/4 expression in HC-11 cells, suggesting that Oct-3/4 induction results from transfer of molecules of < 1 kDa through gap junctions. Inhibition of cAMP signaling in blastomeres abolishes Oct-3/4 expression in somatic cells despite gap junction formation. In addition, reprogramming of NIH3T3 fibroblasts in an extract of HC-11 cells enabled assembly of pCx43 and Oct-3/4 expression after contact of the reprogrammed cells with blastomeres. We propose that gap junction-mediated cAMP signaling between blastomeres and somatic cells results in changes in somatic cell gene expression.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Blastomeres / physiology
  • Cell Communication / drug effects
  • Cell Communication / physiology*
  • Cells, Cultured
  • Connexin 43 / physiology
  • Cyclic AMP / metabolism*
  • DNA-Binding Proteins / biosynthesis*
  • DNA-Binding Proteins / drug effects
  • DNA-Binding Proteins / genetics
  • Embryo, Mammalian
  • Epithelial Cells / drug effects
  • Epithelial Cells / physiology
  • Epithelial Cells / ultrastructure
  • Gap Junctions / drug effects
  • Gap Junctions / physiology*
  • Gap Junctions / ultrastructure
  • Heptanol / pharmacology
  • Hypnotics and Sedatives / pharmacology
  • Immunoblotting
  • Mice
  • Microscopy, Electron
  • Octamer Transcription Factor-3
  • Oleic Acids / pharmacology
  • Transcription Factors / biosynthesis*
  • Transcription Factors / drug effects
  • Transcription Factors / genetics

Substances

  • Connexin 43
  • DNA-Binding Proteins
  • Hypnotics and Sedatives
  • Octamer Transcription Factor-3
  • Oleic Acids
  • Pou5f1 protein, mouse
  • Transcription Factors
  • oleylamide
  • Heptanol
  • Cyclic AMP