Cellular and molecular consequences of calcineurin A alpha gene deletion

Ann N Y Acad Sci. 2007 Nov:1116:216-26. doi: 10.1196/annals.1402.050. Epub 2007 Sep 13.

Abstract

Here we briefly review our studies that have unraveled an important role for the calcium- and calmodulin-sensitive enzyme calcineurin (CN) in bone remodeling. We find that the genetic deletion of the calcineurin Aalpha isoform results in osteoporosis, which is recapitulated in humans following calcineurin inhibitor therapy widely used after solid organ transplantation. Mechanistically, however, while both calcineurin inhibitors cyclosporine and tacrolimus initially stimulate osteoclastic bone resorption in humans, the predominant feature in the CNAalpha null mouse is a profound reduction in bone formation. We speculate that the so-called "calcineurin inhibitors" may interact with molecules other than calcineurin. The clinical relevance of these observations is explored.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Bone Remodeling
  • Calcineurin / genetics*
  • Calcineurin / metabolism
  • Calcineurin Inhibitors
  • Cyclosporine / pharmacology
  • Gene Deletion*
  • Homozygote
  • Humans
  • Immunosuppressive Agents / pharmacology
  • Osteoblasts / metabolism
  • Tacrolimus / pharmacology

Substances

  • Calcineurin Inhibitors
  • Immunosuppressive Agents
  • Cyclosporine
  • Calcineurin
  • PPP3CA protein, human
  • Tacrolimus