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背侧和中间海马体中奖励位置的不同编码。

Different encoding of reward location in dorsal and intermediate hippocampus.

机构信息

Department of Physiology, Development and Neuroscience, Physiological Laboratory, Cambridge CB2 3EG, UK.

Institute of Neuroinformatics, University and ETH Zürich, Winterthurerstrasse 190, Zürich, Switzerland.

出版信息

Curr Biol. 2022 Feb 28;32(4):834-841.e5. doi: 10.1016/j.cub.2021.12.024. Epub 2022 Jan 10.

Abstract

Hippocampal place cells fire at specific locations in the environment. They form a cognitive map that encodes spatial relations in the environment, including reward locations. As part of this encoding, dorsal CA1 (dCA1) place cells accumulate at reward. The encoding of learned reward location could vary between the dorsal and intermediate hippocampus, which differ in gene expression and cortical and subcortical connectivity. While the dorsal hippocampus is critical for spatial navigation, the involvement of intermediate CA1 (iCA1) in spatial navigation might depend on task complexity and learning phase. The intermediate-to-ventral hippocampus regulates reward-seeking, but little is known about the involvement in reward-directed navigation. Here, we compared the encoding of learned reward locations in dCA1 and iCA1 during spatial navigation. We used calcium imaging with a head-mounted microscope to track the activity of CA1 cells over multiple days during which mice learned different reward locations. In dCA1, the fraction of active place cells increased in anticipation of reward, but the pool of active cells changed with the reward location. In iCA1, the same cells anticipated multiple reward locations. Our results support a model in which the dCA1 cognitive map incorporates a changing population of cells that encodes reward proximity through increased population activity, while iCA1 provides a reward-predictive code through a dedicated subpopulation. Both of these location-invariant codes persisted over time, and together they provide a dual hippocampal reward location code, assisting goal-directed navigation..

摘要

海马体位置细胞在环境中的特定位置发射。它们形成了一个认知地图,用于编码环境中的空间关系,包括奖励位置。作为这种编码的一部分,背侧 CA1(dCA1)位置细胞在奖励时积累。学习奖励位置的编码可能在背侧和中间海马体之间有所不同,它们在基因表达和皮质和皮质下连接方面存在差异。虽然背侧海马体对空间导航至关重要,但中间 CA1(iCA1)在空间导航中的参与可能取决于任务复杂性和学习阶段。中间至腹侧海马体调节寻求奖励,但对其在奖励导向导航中的参与知之甚少。在这里,我们比较了在空间导航过程中 dCA1 和 iCA1 中学习奖励位置的编码。我们使用带有头戴式显微镜的钙成像技术,在小鼠学习不同奖励位置的多天期间跟踪 CA1 细胞的活动。在 dCA1 中,活跃的位置细胞在预期奖励时增加,但活跃细胞的池随奖励位置而变化。在 iCA1 中,相同的细胞预期多个奖励位置。我们的结果支持了这样一种模型,即 dCA1 认知地图通过增加群体活动来整合一个不断变化的细胞群体,该群体通过增加群体活动来编码奖励接近度,而 iCA1 通过专门的亚群提供奖励预测代码。这两种位置不变的代码都随着时间的推移而持续存在,它们共同提供了一个双海马体奖励位置代码,有助于目标导向导航。

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