Cardiovascular lesions and skeletal myopathy in mice lacking desmin

Dev Biol. 1996 May 1;175(2):362-6. doi: 10.1006/dbio.1996.0122.


In order to further our understanding of the biological role of desmin, the muscle-specific intermediate filament protein, a null mutation in the desmin gene was introduced into the germ line of mice. Despite the complete lack of desmin, these mice developed and reproduced. Since we show that skeletal, cardiac, and smooth muscles form in the Des-/- mice, it is reasonable to propose that desmin is not essential for myogenic commitment or for myoblast fusion or differentiation in vivo. However, morphological abnormalities were observed in the diaphragm of adult mice; these were demonstrated by disorganized, distended, and nonaligned fibers. The heart presented areas of hemorrhaging in which fibrosis and ischemia were observed. We have also shown that the absence of desmin produces specific defects in smooth muscles. In conclusion, our results have demonstrated that desmin is not required for the differentiation of skeletal, cardiac, and smooth muscles but is essential to strengthen and maintain the integrity of these tissues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Desmin / deficiency*
  • Desmin / genetics
  • Desmin / physiology
  • Diaphragm / abnormalities
  • Diaphragm / pathology
  • Fertility
  • Fetal Heart / metabolism
  • Heart Defects, Congenital / genetics*
  • Heart Defects, Congenital / metabolism
  • Heart Defects, Congenital / pathology
  • Intermediate Filaments / metabolism
  • Intermediate Filaments / pathology
  • Mice
  • Mice, Inbred DBA
  • Mice, Knockout
  • Muscle, Skeletal / abnormalities*
  • Muscle, Skeletal / embryology
  • Muscle, Skeletal / pathology
  • Muscle, Smooth / abnormalities
  • Muscle, Smooth / embryology
  • Muscle, Smooth / pathology
  • Myocardium / pathology
  • Myofibrils / metabolism
  • Myofibrils / ultrastructure


  • Desmin