Loss of desmoglein 2 suggests essential functions for early embryonic development and proliferation of embryonal stem cells

Eur J Cell Biol. 2002 Nov;81(11):592-8. doi: 10.1078/0171-9335-00278.

Abstract

Desmoglein 2 (Dsg2) is a Ca(2+)-dependent adhesion molecule of desmosomes and is synthesized in all desmosome-bearing tissues from their earliest appearance onward. To examine the function of Dsg2, its gene was inactivated by homologous recombination in embryonal stem (ES) cells for the generation of knockout mice. DSG2 -/- mice and a considerable number of DSG2 +/- mice died at or shortly after implantation. On the other hand, DSG2 -/- blastocysts developed an apparently normal trophectoderm layer, the first tissue known to produce desmosomes, and hatched properly. Immunofluorescence analyses of these blastocysts showed, however, that the distribution of the desmosomal plaque protein desmoplakin was disturbed, whereas the adherens junction proteins E-cadherin and beta-catenin appeared to be unaffected. Unexpectedly, we found that Dsg2 seems to be essential for the inner cell mass and the ES cell population derived there from. We present evidence that Dsg2, which is located in desmoplakin-negative wild-type ES cells in non-desmosomal junctions, is needed for normal ES cell proliferation. Our observations thus reveal that important Dsg2 functions are desmosome-independent during early development and are needed for ES cell and early embryo survival.

Publication types

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

MeSH terms

  • Animals
  • Blastocyst / physiology*
  • Cadherins / metabolism
  • Cytoskeletal Proteins / metabolism
  • Cytoskeletal Proteins / physiology*
  • Desmoglein 2
  • Desmogleins
  • Desmoplakins
  • Embryo, Mammalian
  • Embryonic and Fetal Development / physiology*
  • Female
  • Fluorescent Antibody Technique
  • Gap Junctions / physiology*
  • Gap Junctions / ultrastructure
  • Immunoblotting
  • Male
  • Mice
  • Mice, Knockout
  • Microscopy, Electron
  • Stem Cells / physiology
  • Stem Cells / ultrastructure
  • Trans-Activators / metabolism
  • beta Catenin

Substances

  • CTNNB1 protein, mouse
  • Cadherins
  • Cytoskeletal Proteins
  • Desmoglein 2
  • Desmogleins
  • Desmoplakins
  • Dsg2 protein, mouse
  • Dsp protein, mouse
  • Trans-Activators
  • beta Catenin