Memory trace interference impairs recall in a mouse model of Alzheimer's disease

被引:36
|
作者
Poll, Stefanie [1 ]
Mittag, Manuel [1 ]
Musacchio, Fabrizio [1 ]
Justus, Lena C. [1 ]
Giovannetti, Eleonora Ambrad [1 ]
Steffen, Julia [1 ]
Wagner, Jens [1 ]
Zohren, Lioba [2 ]
Schoch, Susanne [2 ]
Schmidt, Boris [3 ]
Jackson, Walker S. [4 ]
Ehninger, Dan [5 ]
Fuhrmann, Martin [1 ]
机构
[1] German Ctr Neurodegenerat Dis DZNE, Neuroimmunol & Imaging Grp, Bonn, Germany
[2] Univ Bonn, Inst Neuropathol, Bonn, Germany
[3] Tech Univ Darmstadt, Clemens Schopf Inst, Darmstadt, Germany
[4] German Ctr Neurodegenerat Dis DZNE, Select Vulnerabil Neurodegenerat Dis, Bonn, Germany
[5] German Ctr Neurodegenerat Dis DZNE, Mol & Cellular Cognit Grp, Bonn, Germany
关键词
IN-VIVO; C-FOS; SYNAPTIC PLASTICITY; ENGRAM CELLS; HIPPOCAMPUS; EXPRESSION; INFORMATION; EXPERIENCE; RETRIEVAL; DYNAMICS;
D O I
10.1038/s41593-020-0652-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mice with AD-like pathology and memory impairments surprisingly have memory engrams in their hippocampus. However, interference with novelty-like cells prevents proper recall, erroneously letting mice perceive a previously learned context as novel. In Alzheimer's disease (AD), hippocampus-dependent memories underlie an extensive decline. The neuronal ensemble encoding a memory, termed engram, is partially recapitulated during memory recall. Artificial activation of an engram can restore memory in a mouse model of early AD, but its fate and the factors that render the engram nonfunctional are yet to be revealed. Here, we used repeated two-photon in vivo imaging to analyze fosGFP transgenic mice (which express enhanced GFP under the Fos promoter) performing a hippocampus-dependent memory task. We found that partial reactivation of the CA1 engram during recall is preserved under AD-like conditions. However, we identified a novelty-like ensemble that interfered with the engram and thus compromised recall. Mimicking a novelty-like ensemble in healthy mice was sufficient to affect memory recall. In turn, reducing the novelty-like signal rescued the recall impairment under AD-like conditions. These findings suggest a novel mechanistic process that contributes to the deterioration of memories in AD.
引用
收藏
页码:952 / +
页数:23
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