The role of beta-catenin stability in mutant PS1-associated apoptosis

Neuroreport. 1999 Aug 20;10(12):2527-32. doi: 10.1097/00001756-199908200-00017.

Abstract

Most early onset cases of familial Alzheimer's disease (FAD) are caused by mutations in presenilin-1 (PS1) and presenilin-2 (PS2). These mutations lead to increased beta-amyloid formation and induce apoptosis when expressed in vitro. Recently, PS1 has been reported to associate with beta-catenin, an armadillo repeat protein. PS1 may regulate the function of beta-catenin, and mutant PS1 may disrupt this regulation. In the present study, we confirm that PS1-WT, as well as mutant PS1, associates with beta-catenin, and that mutant PS1 expression decreases the stability and/or enhances the degradation of beta-catenin. Most importantly, we correlate beta-catenin's destabilization with mutant PS1-associated apoptosis by administering drugs that alter the stability of beta-catenin. The application of LiCl and a proteasome inhibitor, N-acetyl-leu-leu-norleucinal (ALLN), increased the stability of cytosolic beta-catenin in mutant PS1-expressing cells leading to rescue of these cells from apoptosis. These studies suggest that beta-catenin is a key mediator of mutant PS1-associated apoptosis and FAD pathogenesis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alzheimer Disease / genetics
  • Alzheimer Disease / physiopathology*
  • Animals
  • Apoptosis / physiology*
  • Cadherins / physiology*
  • Cell Line
  • Cytoskeletal Proteins / physiology*
  • Genetic Vectors
  • Humans
  • Membrane Proteins / genetics*
  • Mutation
  • PC12 Cells
  • Presenilin-1
  • Rats
  • Retroviridae / genetics
  • Trans-Activators*
  • Virus Replication
  • beta Catenin

Substances

  • CTNNB1 protein, human
  • Cadherins
  • Ctnnb1 protein, rat
  • Cytoskeletal Proteins
  • Membrane Proteins
  • PSEN1 protein, human
  • Presenilin-1
  • Trans-Activators
  • beta Catenin