Functionally Distinct Neuronal Ensembles within the Memory Engram

• Published in: Cell Vol. 181; no. 2; pp. 410 - 423.e17
• Main Authors: Sun, Xiaochen, Bernstein, Max J., Meng, Meizhen, Rao, Siyuan, Sørensen, Andreas T., Yao, Li, Zhang, Xiaohui, Anikeeva, Polina O., Lin, Yingxi
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 16.04.2020
• Subjects: activity-dependent pathways; Animals; Basic Helix-Loop-Helix Transcription Factors - metabolism; brain; Brain - physiology; CCK+ interneurons; cortex; dentate gyrus; Dentate Gyrus - physiology; Fear - physiology; fearfulness; Fos; interneurons; Interneurons - physiology; Male; medial entorhinal cortex; memory; Memory - physiology; memory discrimination; memory engram; memory generalization; Mice; Mice, Inbred C57BL; neuronal ensembles; Neurons - metabolism; Neurons - physiology; Npas4; Proto-Oncogene Proteins c-fos - metabolism; synaptic transmission; transcription (genetics); memory engram; neuronal ensembles; dentate gyrus; CCK+ interneurons; activity-dependent pathways; Fos; medial entorhinal cortex; memory discrimination; memory generalization; Npas4; CCK(+) interneurons
• ISSN: 0092-8674; 1097-4172; 1097-4172
• DOI: 10.1016/j.cell.2020.02.055

Memories are believed to be encoded by sparse ensembles of neurons in the brain. However, it remains unclear whether there is functional heterogeneity within individual memory engrams, i.e., if separate neuronal subpopulations encode distinct aspects of the memory and drive memory expression differently. Here, we show that contextual fear memory engrams in the mouse dentate gyrus contain functionally distinct neuronal ensembles, genetically defined by the Fos- or Npas4-dependent transcriptional pathways. The Fos-dependent ensemble promotes memory generalization and receives enhanced excitatory synaptic inputs from the medial entorhinal cortex, which we find itself also mediates generalization. The Npas4-dependent ensemble promotes memory discrimination and receives enhanced inhibitory drive from local cholecystokinin-expressing interneurons, the activity of which is required for discrimination. Our study provides causal evidence for functional heterogeneity within the memory engram and reveals synaptic and circuit mechanisms used by each ensemble to regulate the memory discrimination-generalization balance. [Display omitted] •Functionally distinct neuronal ensembles exist within a single memory engram•Fos- and Npas4-dependent ensembles undergo distinct synaptic modifications after CFC•Fos- and Npas4-dependent ensembles drive memory-guided behaviors in opposite directions•Memory generalization and discrimination, respectively, require MEC and CCK+ interneurons Two functionally distinct neuronal ensembles within a single memory engram undergo different learning-induced synaptic modifications and drive memory-guided behaviors in opposite directions.