The essential role of p53-up-regulated modulator of apoptosis (Puma) and its regulation by FoxO3a transcription factor in β-amyloid-induced neuron death

J Biol Chem. 2014 Apr 11;289(15):10812-10822. doi: 10.1074/jbc.M113.519355. Epub 2014 Feb 24.

Abstract

Neurodegeneration underlies the pathology of Alzheimer disease (AD). The molecules responsible for such neurodegeneration in AD brain are mostly unknown. Recent findings indicate that the BH3-only proteins of the Bcl-2 family play an essential role in various cell death paradigms, including neurodegeneration. Here we report that Puma (p53-up-regulated modulator of apoptosis), an important member of the BH3-only protein family, is up-regulated in neurons upon toxic β-amyloid 1-42 (Aβ(1-42)) exposure both in vitro and in vivo. Down-regulation of Puma by specific siRNA provides significant protection against neuron death induced by Aβ(1-42). We further demonstrate that the activation of p53 and inhibition of PI3K/Akt pathways induce Puma. The transcription factor FoxO3a, which is activated when PI3K/Akt signaling is inhibited, directly binds with the Puma gene and induces its expression upon exposure of neurons to oligomeric Aβ(1-42). Moreover, Puma cooperates with another BH3-only protein, Bim, which is already implicated in AD. Our results thus suggest that Puma is activated by both p53 and PI3K/Akt/FoxO3a pathways and cooperates with Bim to induce neuron death in response to Aβ(1-42).

Keywords: Alzheimer Disease; Amyloid; Bcl-2 Family Proteins; Bim; Cell Death; Foxo; Neurodegeneration; Neurons; Puma; siRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / metabolism*
  • Amyloid beta-Peptides / pharmacology*
  • Animals
  • Apoptosis
  • Apoptosis Regulatory Proteins / genetics
  • Apoptosis Regulatory Proteins / metabolism*
  • Brain / pathology
  • Cell Death
  • Cells, Cultured
  • Forkhead Box Protein O3
  • Forkhead Transcription Factors / metabolism*
  • Male
  • Mutagenesis, Site-Directed
  • Neurons / metabolism*
  • Neurons / pathology
  • PC12 Cells
  • Peptide Fragments / pharmacology*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction
  • Time Factors
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Amyloid beta-Peptides
  • Apoptosis Regulatory Proteins
  • Bbc3 protein, rat
  • FOXO3 protein, rat
  • Forkhead Box Protein O3
  • Forkhead Transcription Factors
  • Peptide Fragments
  • Proto-Oncogene Proteins c-bcl-2
  • Tumor Suppressor Protein p53
  • amyloid beta-protein (1-42)