Granular non-fibrillar aggregates and toxicity in Alzheimer's disease

Curr Alzheimer Res. 2012 Oct;9(8):962-71. doi: 10.2174/156720512803251129.

Abstract

Granular non-fibrillar aggregates (GNAs) are identified as possible toxic species in Alzheimer's disease. GNAs form on the surface of negatively charged biological membranes and as a consequence of an acidic environment, off the polymerization pathway at neutral pH. Aβ (1-40) GNAs disturb the bilayer structure of model membranes and seem to be more toxic to cells with negatively charged membranes (consequence of chronic pre-apoptosis). GNAs may be relevant in physiological situations associated to Alzheimer's disease: a local acidic pH at the cell surface (consequence of lipid oxidation or other cell insults) and acidification as a consequence of vascular events causing hypoxia. Together with previous descriptions of granular aggregates with poly-glutamine peptides related to Huntington's disease and the SH3 domain of PI3, GNAs related to Alzheimer's disease are a further example of a possible common aggregation and toxicity mechanism in conformational diseases. GNAs may represent a new pharmacological target in Alzheimer's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / metabolism
  • Alzheimer Disease / pathology*
  • Amyloid beta-Peptides / chemistry
  • Amyloid beta-Peptides / metabolism
  • Amyloid beta-Peptides / toxicity*
  • Animals
  • Cell Membrane / chemistry
  • Cell Membrane / metabolism
  • Flow Cytometry
  • Humans
  • Hydrogen-Ion Concentration
  • Lipid Peroxidation / physiology
  • Liposomes / chemistry
  • Liposomes / metabolism*
  • Microscopy, Atomic Force
  • Microscopy, Electron, Transmission
  • Neurons / metabolism
  • PC12 Cells
  • Peptide Fragments / chemistry
  • Peptide Fragments / metabolism
  • Peptide Fragments / toxicity*
  • Rats

Substances

  • Amyloid beta-Peptides
  • Liposomes
  • Peptide Fragments
  • amyloid beta-protein (1-40)