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Neuroreport. 2004 Dec 3;15(17):2655-8.

ApoE isoform affects LTP in human targeted replacement mice.

Author information

1
Department of Pediatrics, Alzheimer's Disease Core Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60614, USA. btrommer@northwestern.edu

Abstract

Inheritance of the epsilon4 allele for apolipoprotein E (apoE) increases the risk of Alzheimer disease and memory impairment, whereas epsilon2 decreases these risks compared with the most common epsilon3 allele, but the mechanism for these effects is unknown. Long-term potentiation (LTP) is an experimentally induced increase in synaptic efficacy that models memory. Using hippocampal slices from wild type (WT), apoE knockout (apoE-KO), and targeted replacement mice expressing human apoE2, E3, or E4 (apoE-TR) we found that although all strains had comparable basal synaptic transmission, LTP was significantly greater in WT and apoE3-TR than in apoE-KO, apoE2-TR or apoE4-TR. This novel system may be used to investigate the mechanisms of apoE isoform dependent modulation of susceptibility to memory impairment.

PMID:
15570172
[Indexed for MEDLINE]

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