Regional and interhemispheric differences of neuronal representations in dentate gyrus and CA3 inferred from expression of zif268.

The hippocampal formation is one of the best studied brain regions for spatial and mnemonic representations. These representations have been reported to differ in their properties for individual hippocampal subregions. One approach that allows the detection of neuronal representations is immediate early gene imaging, which relies on the visualization of genomic responses of activated neuronal populations, so called engrams. This method permits the within-animal comparison of neuronal representations across different subregions. In this work, we have used compartmental analysis of temporal activity by fluorescence in-situ hybridisation (catFISH) of the immediate early gene zif268/erg1 to compare neuronal representations between subdivisions of the dentate gyrus and CA3 upon exploration of different contexts. Our findings give an account of subregion-specific ensemble sizes. We confirm previous results regarding disambiguation abilities in dentate gyrus and CA3 but in addition report novel findings: Although ensemble sizes in the lower blade of the dentate gyrus are significantly smaller than in the upper blade both blades are responsive to environmental change. Beyond this, we show significant differences in the representation of familiar and novel environments along the longitudinal axis of dorsal CA3 and most interestingly between CA3 regions of both hemispheres.

Task-specific oscillatory synchronization of prefrontal cortex, nucleus reuniens, and hippocampus during working memory.

Working memory requires maintenance of and executive control over task-relevant information on a timescale of seconds. Spatial working memory depends on interactions between hippocampus, for the representation of space, and prefrontal cortex, for executive control. A monosynaptic hippocampal projection to the prefrontal cortex has been proposed to serve this interaction. However, connectivity and inactivation experiments indicate a critical role of the nucleus reuniens in hippocampal-prefrontal communication. We have investigated the dynamics of oscillatory coherence throughout the prefrontal-hippocampal-reuniens network in a touchscreen-based working memory task. We found that coherence at distinct frequencies evolved depending on phase and difficulty of the task. During choice, the reuniens did not participate in enhanced prefrontal-hippocampal theta but in gamma coherence. Strikingly, the reuniens was strongly embedded in performance-related increases in beta coherence, suggesting the execution of top-down control. In addition, we show that during working memory maintenance the prefrontal-hippocampal-reuniens network displays performance-related delay activity.