Identification of an engram ensemble mediating memory forgetting in the dentate gyrus
- Neuron. 2026 Feb 18;114(4):759-773.e5. doi: 10.1016/j.neuron.2025.12.031.
- 1. School of Life Sciences, IDG/McGovern Institute for Brain Research, MOE Key Laboratory of Protein Sciences, Tsinghua University, Beijing 100084, China; Peking University, Tsinghua University, National Institute Biological Science Joint Graduate Program, Peking, China.
- 2. School of Life Sciences, IDG/McGovern Institute for Brain Research, MOE Key Laboratory of Protein Sciences, Tsinghua University, Beijing 100084, China.
- 3. Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100005, China.
- 4. Honours College of Capital Normal University, Capital Normal University, Beijing, China.
- 5. School of Life Sciences, IDG/McGovern Institute for Brain Research, MOE Key Laboratory of Protein Sciences, Tsinghua University, Beijing 100084, China; Tsinghua-Peking Center for Life Sciences, Beijing 100084, China.
- 6. School of Life Sciences, IDG/McGovern Institute for Brain Research, MOE Key Laboratory of Protein Sciences, Tsinghua University, Beijing 100084, China; Peking University, Tsinghua University, National Institute Biological Science Joint Graduate Program, Peking, China; Tsinghua-Peking Center for Life Sciences, Beijing 100084, China. Electronic address: [email protected].
How the memory engram is organized at the cell-assembly level to support not only encoding of learned information but also memory flexibility remains elusive. Here, we propose a novel engram model encoded by two orthogonal learning-recruited neuronal ensembles in the mouse dentate gyrus. Reactivation of the Fos-tagged ensemble promotes memory retrieval, whereas reactivation of the Npas4-dependent ensemble drives forgetting, with manipulation of the forgetting ensemble inversely shifting memory ensemble reactivation. Such encoding enables flexibility in recall outcomes, ranging from full-scale memory expression to complete forgetting. Meanwhile, learned information remains unperturbed, as reactivation modifications specifically target the forgetting ensemble by regulating Rac1 activity, which is sensitive to cognitive and emotional events. Notably, memory abnormalities observed in mouse models of Alzheimer's disease and autism are primarily linked to dysfunctions of the forgetting ensemble, suggesting that the mechanism underlying forgetting represents a major target for cognitive disorders.
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Research Areas: Others