海马体CA1区经验依赖的位置细胞参照机制

IF 20 1区 医学 Q1 NEUROSCIENCES Nature neuroscience Pub Date : 2025-04-01 DOI:10.1038/s41593-025-01930-5
Fish Kunxun Qian, Yiding Li, Jeffrey C. Magee
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摘要

海马体CA1位置细胞(pc)编码空间和目标参考信息,以支持认知地图。这种参照的机制和经验的作用仍然知之甚少。在这里,我们纵向记录了头部固定的小鼠在跑步机上执行空间学习任务时的PC活动。在熟悉的环境中,CA1表征由pc组成,这些pc以大约相等的比例被引用到特定的空间位置或奖励目标;然而,CA1表示在暴露于新环境时主要是目标参考,因为空间参考pc自适应地切换参考帧。细胞膜电位记录显示,单个CA1神经元同时接收空间参考和目标参考突触输入,这些输入的比例与单个PC参考相关。此外,行为时间尺度突触可塑性形成PC参考。综上所述,这些结果表明突触输入的经验依赖性调整塑造了PC参考,以支持灵活的认知地图。
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Mechanisms of experience-dependent place-cell referencing in hippocampal area CA1
Hippocampal CA1 place cells (PCs) encode both space- and goal-referenced information to support a cognitive map. The mechanism of this referencing and the role of experience remain poorly understood. Here we longitudinally recorded PC activity while head-fixed mice performed a spatial learning task on a treadmill. In a familiar environment, the CA1 representation consisted of PCs that were referenced to either specific spatial locations or a reward goal in approximately equal proportions; however, the CA1 representation became predominately goal-referenced upon exposure to a novel environment, as space-referenced PCs adaptively switched reference frames. Intracellular membrane potential recordings revealed that individual CA1 neurons simultaneously received both space- and goal-referenced synaptic inputs, and the ratio of these inputs was correlated with individual PC referencing. Furthermore, behavioral timescale synaptic plasticity shaped PC referencing. Together, these results suggest that experience-dependent adjustment of synaptic input shapes PC referencing to support a flexible cognitive map. Through multiday imaging and acute whole-cell recordings in behaving mice, Qian, Li and Magee provide insight into place field formation in general and specifically how the hippocampus adaptively remaps for flexible goal-directed navigation.
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来源期刊
Nature neuroscience
Nature neuroscience 医学-神经科学
CiteScore
38.60
自引率
1.20%
发文量
212
审稿时长
1 months
期刊介绍: Nature Neuroscience, a multidisciplinary journal, publishes papers of the utmost quality and significance across all realms of neuroscience. The editors welcome contributions spanning molecular, cellular, systems, and cognitive neuroscience, along with psychophysics, computational modeling, and nervous system disorders. While no area is off-limits, studies offering fundamental insights into nervous system function receive priority. The journal offers high visibility to both readers and authors, fostering interdisciplinary communication and accessibility to a broad audience. It maintains high standards of copy editing and production, rigorous peer review, rapid publication, and operates independently from academic societies and other vested interests. In addition to primary research, Nature Neuroscience features news and views, reviews, editorials, commentaries, perspectives, book reviews, and correspondence, aiming to serve as the voice of the global neuroscience community.
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