Alzheimer’s disease-like pathology induced by amyloid-β oligomers in nonhuman primates

Leticia Forny-Germano, Natalia M. Lyra E Silva, André F. Batista, Jordano Brito-Moreira, Matthias Gralle, Susan E. Boehnke, Brian C. Coe, Ann Lablans, Suelen A. Marques, Ana Maria B. Martinez, William L. Klein, Jean Christophe Houzel, Sergio T. Ferreira, Douglas P. Munoz, Fernanda G. De Felice*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

116 Scopus citations

Abstract

Alzheimer’s disease (AD) is a devastating neurodegenerative disorder and a major medical problem. Here, we have investigated the impact of amyloid- β (A β) oligomers, AD-related neurotoxins, in the brains of rats and adult nonhuman primates (cynomolgus macaques). Soluble Aβ oligomers are known to accumulate in the brains of AD patients and correlate with disease-associated cognitive dysfunction. When injected into the lateral ventricle of rats and macaques, Aβ oligomers diffused into the brain and accumulated in several regions associated with memory and cognitive functions. Cardinal features of AD pathology, including synapse loss, tau hyperphosphorylation, astrocyte and microglial activation, were observed in regions of the macaque brain where Aβ oligomers were abundantly detected. Most importantly, oligomer injections induced AD-type neurofibrillary tangle formation in the macaque brain. These outcomes were specifically associated with Aβ oligomers, as fibrillar amyloid deposits were not detected in oligomer-injected brains. Human and macaque brains share significant similarities in terms of overall architecture and functional networks. Thus, generation of a macaque model of AD that links Aβ oligomers to tau and synaptic pathology has the potential to greatly advance our understanding of mechanisms centrally implicated in AD pathogenesis. Furthermore, development of disease-modifying therapeutics for AD has been hampered by the difficulty in translating therapies that work in rodents to humans. This new approach may be a highly relevant nonhuman primate model for testing therapeutic interventions for AD.

Original languageEnglish (US)
Pages (from-to)13629-13643
Number of pages15
JournalJournal of Neuroscience
Volume34
Issue number41
DOIs
StatePublished - Oct 8 2014

Keywords

  • Alzheimer’s disease
  • Amyloid-β oligomers
  • Nonhuman primate
  • Synapse loss
  • Tau pathology

ASJC Scopus subject areas

  • Neuroscience(all)

Fingerprint Dive into the research topics of 'Alzheimer’s disease-like pathology induced by amyloid-β oligomers in nonhuman primates'. Together they form a unique fingerprint.

Cite this