Naturally secreted oligomers of amyloid beta protein potently inhibit hippocampal long-term potentiation in vivo

Nature. 2002 Apr 4;416(6880):535-9. doi: 10.1038/416535a.


Although extensive data support a central pathogenic role for amyloid beta protein (Abeta) in Alzheimer's disease, the amyloid hypothesis remains controversial, in part because a specific neurotoxic species of Abeta and the nature of its effects on synaptic function have not been defined in vivo. Here we report that natural oligomers of human Abeta are formed soon after generation of the peptide within specific intracellular vesicles and are subsequently secreted from the cell. Cerebral microinjection of cell medium containing these oligomers and abundant Abeta monomers but no amyloid fibrils markedly inhibited hippocampal long-term potentiation (LTP) in rats in vivo. Immunodepletion from the medium of all Abeta species completely abrogated this effect. Pretreatment of the medium with insulin-degrading enzyme, which degrades Abeta monomers but not oligomers, did not prevent the inhibition of LTP. Therefore, Abeta oligomers, in the absence of monomers and amyloid fibrils, disrupted synaptic plasticity in vivo at concentrations found in human brain and cerebrospinal fluid. Finally, treatment of cells with gamma-secretase inhibitors prevented oligomer formation at doses that allowed appreciable monomer production, and such medium no longer disrupted LTP, indicating that synaptotoxic Abeta oligomers can be targeted therapeutically.

Publication types

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

MeSH terms

  • Alzheimer Disease / etiology
  • Amyloid Precursor Protein Secretases
  • Amyloid beta-Peptides / chemistry
  • Amyloid beta-Peptides / metabolism*
  • Amyloid beta-Peptides / physiology
  • Animals
  • Aspartic Acid Endopeptidases
  • CHO Cells
  • Cricetinae
  • Culture Media, Conditioned
  • Endopeptidases / metabolism
  • Hippocampus / physiology*
  • Humans
  • Insulysin / metabolism
  • Long-Term Potentiation / physiology*
  • Microsomes / metabolism
  • Plaque, Amyloid / metabolism*
  • Protease Inhibitors / pharmacology
  • Rats
  • Recombinant Proteins


  • Amyloid beta-Peptides
  • Culture Media, Conditioned
  • Protease Inhibitors
  • Recombinant Proteins
  • Amyloid Precursor Protein Secretases
  • Endopeptidases
  • Aspartic Acid Endopeptidases
  • BACE1 protein, human
  • Insulysin