Compound genetic ablation of nidogen 1 and 2 causes basement membrane defects and perinatal lethality in mice

Mol Cell Biol. 2005 Aug;25(15):6846-56. doi: 10.1128/MCB.25.15.6846-6856.2005.


Nidogen 1 and 2 are basement membrane glycoproteins, and previous biochemical and functional studies indicate that they may play a crucial role in basement membrane assembly. While they show a divergent expression pattern in certain adult tissues, both have a similar distribution during development. Gene knockout studies in mice demonstrated that the loss of either isoform has no effect on basement membrane formation and organ development, suggesting complementary functions. Here, we show that this is indeed the case. Deficiency of both nidogens in mice resulted in perinatal lethality. Nidogen 1 and 2 do not appear to be crucial in establishing tissue architecture during organ development; instead, they are essential for late stages of lung development and for maintenance and/or integrity of cardiac tissue. These organ defects are not compatible with postnatal survival. Ultrastructural analysis suggests that the phenotypes directly result from basement membrane changes. However, despite the ubiquitous presence of nidogens in basement membranes, defects do not occur in all tissues or in all basement membranes, suggesting a varying spectrum of roles for nidogens in the basement membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basement Membrane / metabolism
  • Basement Membrane / pathology
  • Calcium-Binding Proteins
  • Cell Adhesion Molecules
  • Cell Differentiation / genetics
  • Heart / embryology
  • Kidney / cytology
  • Kidney / embryology
  • Lung / embryology
  • Membrane Glycoproteins / deficiency*
  • Membrane Glycoproteins / genetics*
  • Membrane Glycoproteins / metabolism
  • Membrane Glycoproteins / physiology
  • Mice
  • Mutation
  • Protein Isoforms / deficiency*
  • Protein Isoforms / genetics*
  • Protein Isoforms / physiology


  • Calcium-Binding Proteins
  • Cell Adhesion Molecules
  • Membrane Glycoproteins
  • Nid2 protein, mouse
  • Protein Isoforms
  • nidogen