O-GlcNAcylation increases non-amyloidogenic processing of the amyloid-β precursor protein (APP)

Biochem Biophys Res Commun. 2011 Jan 21;404(3):882-6. doi: 10.1016/j.bbrc.2010.12.080. Epub 2010 Dec 21.

Abstract

The amyloid-β precursor protein (APP) was shown to be O-GlcNAcylated 15 years ago, but the effect of this modification on APP processing and formation of the Alzheimer's disease associated amyloid-β (Aβ) peptide has so far not been investigated. Here, we demonstrate with pharmacological tools or siRNA that O-GlcNAcase and O-GlcNAc transferase regulate the level of O-GlcNAcylated APP. We also show that O-GlcNAcylation increases non-amyloidogenic α-secretase processing, resulting in increased levels of the neuroprotective sAPPα fragment and decreased Aβ secretion. Our results implicate O-GlcNAcylation as a potential therapeutic target for Alzheimer's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylglucosamine / analogs & derivatives
  • Acetylglucosamine / genetics
  • Acetylglucosamine / metabolism*
  • Acetylglucosamine / pharmacology
  • Acylation / drug effects
  • Acylation / genetics
  • Alzheimer Disease / enzymology*
  • Alzheimer Disease / therapy
  • Amyloid beta-Protein Precursor / metabolism*
  • Cell Line, Tumor
  • Gene Knockdown Techniques
  • Humans
  • N-Acetylglucosaminyltransferases / genetics
  • N-Acetylglucosaminyltransferases / metabolism*
  • Oximes / pharmacology
  • Phenylcarbamates / pharmacology
  • RNA, Small Interfering / genetics
  • beta-N-Acetylhexosaminidases / antagonists & inhibitors
  • beta-N-Acetylhexosaminidases / genetics
  • beta-N-Acetylhexosaminidases / metabolism*

Substances

  • APP protein, human
  • Amyloid beta-Protein Precursor
  • Oximes
  • Phenylcarbamates
  • RNA, Small Interfering
  • N-acetylglucosaminono-1,5-lactone O-(phenylcarbamoyl)oxime
  • N-Acetylglucosaminyltransferases
  • hexosaminidase C
  • beta-N-Acetylhexosaminidases
  • Acetylglucosamine