Gillespie Anna K, Jones Emily A, Lin Yuan-Hung, Karlsson Mattias P, Kay Kenneth, Yoon Seo Yeon, Tong Leslie M, Nova Philip, Carr Jessie S, Frank Loren M, Huang Yadong
Gladstone Institute of Neurological Disease, Gladstone Institutes, San Francisco, CA 94158, USA; Biomedical Sciences Graduate Program, University of California, San Francisco, CA 94143, USA.
Gladstone Institute of Neurological Disease, Gladstone Institutes, San Francisco, CA 94158, USA; Neuroscience Graduate Program, University of California, San Francisco, CA 94143, USA.
Neuron. 2016 May 18;90(4):740-51. doi: 10.1016/j.neuron.2016.04.009. Epub 2016 May 5.
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.
载脂蛋白(apo)E4是阿尔茨海默病(AD)的主要遗传风险因素,但其导致认知衰退的机制尚不清楚。在基因敲入(KI)小鼠中,人类apoE4会导致年龄依赖性的学习和记忆障碍以及海马齿状回中GABA能中间神经元的退化。在此,我们报告了两种涉及尖波涟漪(SWRs)的功能性apoE4-KI表型,SWRs是对记忆过程至关重要的海马网络事件。老年apoE4-KI小鼠的SWRs比apoE3-KI小鼠少,且在SWRs期间慢γ活动显著减少。消除GABA能中间神经元中的apoE4可防止学习和记忆障碍,挽救了与SWR相关的慢γ活动,但并未挽救老年小鼠的SWR丰度。年轻和老年apoE4-KI小鼠的SWR丰度均有类似程度的降低;然而,与SWR相关的慢γ活动的完全缺失仅出现在老年apoE4-KI小鼠中。这些结果表明,SWRs期间中间神经元介导的慢γ活动的逐渐衰退是apoE4介导的学习和记忆障碍的关键因素。视频摘要。