| Literature DB >> 27161522 |
Anna K Gillespie1, Emily A Jones1, Yuan-Hung Lin2, Mattias P Karlsson3, Kenneth Kay4, Seo Yeon Yoon5, Leslie M Tong1, Philip Nova1, Jessie S Carr6, Loren M Frank7, Yadong Huang8.
Abstract
Apolipoprotein (apo) E4 is the major genetic risk factor for Alzheimer's disease (AD), but the mechanism by which it causes cognitive decline is unclear. In knockin (KI) mice, human apoE4 causes age-dependent learning and memory impairments and degeneration of GABAergic interneurons in the hippocampal dentate gyrus. Here we report two functional apoE4-KI phenotypes involving sharp-wave ripples (SWRs), hippocampal network events critical for memory processes. Aged apoE4-KI mice had fewer SWRs than apoE3-KI mice and significantly reduced slow gamma activity during SWRs. Elimination of apoE4 in GABAergic interneurons, which prevents learning and memory impairments, rescued SWR-associated slow gamma activity but not SWR abundance in aged mice. SWR abundance was reduced similarly in young and aged apoE4-KI mice; however, the full SWR-associated slow gamma deficit emerged only in aged apoE4-KI mice. These results suggest that progressive decline of interneuron-enabled slow gamma activity during SWRs critically contributes to apoE4-mediated learning and memory impairments. VIDEO ABSTRACT.Entities:
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Year: 2016 PMID: 27161522 PMCID: PMC5097044 DOI: 10.1016/j.neuron.2016.04.009
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173