Kinsky Nathaniel R, Orlin Daniel J, Ruesch Evan A, Kim Brian, Coello Siria, Diba Kamran, Ramirez Steve
Department of Anesthesiology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Neuroscience Graduate Program, Oregon Health & Science University, Portland, OR 97239, USA.
Cell Rep. 2025 Mar 25;44(3):115391. doi: 10.1016/j.celrep.2025.115391. Epub 2025 Mar 8.
Memories involving the hippocampus can take several days to consolidate, challenging efforts to uncover the neuronal signatures underlying this process. Here, we use calcium imaging in freely moving mice to track the hippocampal dynamics underlying memory consolidation across a 10-day contextual fear conditioning task. We find two neural signatures that emerge following learning and predict memory performance: context-specific place field remapping and coordinated neural activity prior to memory recall (freezing). To test whether these signatures support memory consolidation, we pharmacologically induced amnesia in separate mice by administering anisomycin, a protein synthesis inhibitor, immediately following learning. We find that anisomycin paradoxically accelerates cell turnover. Anisomycin also arrests learning-related remapping and blocks coordinated activity predictive of memory-related freezing behavior, effects that are likewise absent in untreated mice that exhibit poor memory expression. We conclude that context-specific place field remapping and the development of coordinated ensemble activity underlie contextual memory consolidation.
涉及海马体的记忆需要几天时间来巩固,这给揭示这一过程背后的神经元特征带来了挑战。在这里,我们在自由活动的小鼠中使用钙成像技术,以追踪在一项为期10天的情境恐惧条件反射任务中记忆巩固背后的海马体动态变化。我们发现了两种在学习后出现并预测记忆表现的神经特征:特定情境的位置场重映射以及记忆回忆(僵住)之前的协调神经活动。为了测试这些特征是否支持记忆巩固,我们在单独的小鼠学习后立即给予蛋白质合成抑制剂茴香霉素,通过药物诱导失忆。我们发现茴香霉素出人意料地加速了细胞更替。茴香霉素还会阻止与学习相关的重映射,并阻断预测与记忆相关的僵住行为的协调活动,而在记忆表达不佳的未处理小鼠中同样不存在这些效应。我们得出结论,特定情境的位置场重映射和协调集合活动的发展是情境记忆巩固的基础。