Sphingolipid storage impairs autophagic clearance of Alzheimer-associated proteins

Autophagy. 2011 Jun;7(6):645-6. doi: 10.4161/auto.7.6.15122. Epub 2011 Jun 1.

Abstract

Recent work from our laboratory demonstrates that the accumulation of sphingolipids (SLs) decreases the capacity of cells to clear potentially amyloidogenic fragments of the amyloid precursor protein (APP) during autophagy. APP is a type I membrane protein and could undergo sequential proteolytic processing by β- and γ-secretase resulting in the generation of the amyloid β-peptide (Aβ). Genetic, molecular and biochemical evidence indicates that the accumulation of toxic Aβ aggregates plays a critical role in the degeneration of neurons during the pathogenesis of Alzheimer disease (AD). Thus, SL storage could promote the accumulation of Ab in endosomal and lysosomal compartments and thereby induce characteristic cytopathological changes of AD.

MeSH terms

  • Alzheimer Disease / metabolism*
  • Amyloid Precursor Protein Secretases / metabolism
  • Amyloid beta-Peptides / metabolism
  • Amyloid beta-Protein Precursor / metabolism*
  • Animals
  • Autophagy
  • Cell Membrane / metabolism
  • Endosomes / metabolism
  • Humans
  • Lysosomes / metabolism
  • Models, Biological
  • Neurons / metabolism
  • Sphingolipids / metabolism*

Substances

  • APP protein, human
  • Amyloid beta-Peptides
  • Amyloid beta-Protein Precursor
  • Sphingolipids
  • Amyloid Precursor Protein Secretases