Aβ42 neurotoxicity in primary co-cultures: Effect of apoE isoform and Aβ conformation

Abstract 

Autosomal dominant mutations that increase amyloid-β(1–42) (Aβ42) cause familial Alzheimer's disease (AD), and the most common genetic risk factor for AD is the presence of the ɛ4 allele of apolipoprotein E (apoE). Previously, we characterized stable preparations of Aβ42 oligomers and fibrils and reported that oligomers induced a 10-fold greater increase in neurotoxicity than fibrils in Neuro-2A cells. To determine the effects of apoE genotype on Aβ42 oligomer- and fibril-induced neurotoxicity in vitro, we co-cultured wild type (WT) neurons with glia from WT, apoE-knockout (apoE-KO), and human apoE2-, E3-, and E4-targeted replacement (TR) mice. Dose-dependent neurotoxicity was induced by oligomeric Aβ42 with a ranking order of apoE4-TR>KO=apoE2-TR=apoE3-TR>WT. Neurotoxicity induced by staurosporine or glutamate were not affected by apoE genotype, indicating specificity for oligomeric Aβ42-induced neurotoxicity. These in vitro data demonstrate a gain of negative function for apoE4, synergistic with oligomeric Aβ42, in mediating neurotoxicity.

Keywords: ApoE, Alzheimer disease, Amyloid-β, Neurotoxicity, Co-cultures, ApoE transgenic mice