Hippocampal Memory Traces Are Differentially Modulated by Experience, Time, and Adult Neurogenesis

被引:379
作者
Denny, Christine A. [1 ,2 ,4 ]
Kheirbek, Mazen A. [2 ,4 ]
Alba, Eva L. [2 ,4 ]
Tanaka, Kenji F. [2 ,3 ,4 ]
Brachman, Rebecca A. [2 ]
Laughman, Kimberly B. [1 ]
Tomm, Nicole K. [2 ]
Turi, Gergely F. [2 ]
Losonczy, Attila [2 ]
Hen, Rene [2 ,3 ,4 ]
机构
[1] Columbia Univ, Dept Biol Sci, New York, NY 10032 USA
[2] Columbia Univ, Dept Neurosci & Psychiat, New York, NY 10032 USA
[3] Columbia Univ, Dept Pharmacol, New York, NY 10032 USA
[4] New York State Psychiat Inst & Hosp, Div Integrat Neurosci, New York, NY 10032 USA
关键词
IMMEDIATE-EARLY GENE; DENTATE GYRUS; PATTERN SEPARATION; SYNAPTIC PLASTICITY; REGULATED GENE; FEAR MEMORY; CA3; NEURONS; EXPRESSION; RETRIEVAL;
D O I
10.1016/j.neuron.2014.05.018
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Memory traces are believed to be ensembles of cells used to store memories. To visualize memory traces, we created a transgenic line that allows for the comparison between cells activated during encoding and expression of a memory. Mice re-exposed to a fear-inducing context froze more and had a greater percentage of reactivated cells in the dentate gyrus (DG) and CA3 than mice exposed to a novel context. Over time, these differences disappeared, in keeping with the observation that memories become generalized. Optogenetically silencing DG or CA3 cells that were recruited during encoding of a fear-inducing context prevented expression of the corresponding memory. Mice with reduced neurogenesis displayed less contextual memory and less reactivation in CA3 but, surprisingly, normal reactivation in the DG. These studies suggest that distinct memory traces are located in the DG and in CA3 but that the strength of the memory is related to reactivation in CA3.
引用
收藏
页码:189 / 201
页数:13
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