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Brizee, D.

Publications and source records attributed to Brizee, D..

2 recordsLinked to original sources

Spatio-temporal organization of network activity patterns in the hippocampus

The hippocampus is a layered brain network, composed of diverse cell types arranged in multiple microcircuits with anatomically structured inputs, all working in concert to support memory. This intricate organization generates a myriad of electrophysiological signatures. While specific aspects of these activity patterns have been explored, a comprehensive understanding of the hippocampal layer-embedded dynamics remains elusive. Here, we developed a low-dimensional manifold to capture electrophysiological patterns, mapping their anatomical trajectory along the CA1-to-DG axis, and distinguishing layers based on sharp-wave and theta profiles. This profiling led to the characterization of selective theta-nested gamma signatures for each layer. It further revealed spike patterns associated with gamma rhythms, which highlight specific firing motifs between principal cells and interneurons, and differential firing properties within pyramidal sub-layers. These findings support a holistic understanding of the spatio-temporal activity patterns across hippocampal layers for unraveling the network operations that drive memory-guided behavior.

neuroscience↗

Organizing the coactivity structure of the hippocampus from robust to flexible memory

New memories are integrated into prior knowledge of the world. But what if consecutive memories exert opposing demands on the host brain network? We report that acquiring a robust (food-context) memory constrains the hippocampus within a population activity space of highly correlated spike trains that prevents subsequent computation of a flexible (object-location) memory. This densely correlated firing structure developed over repeated mnemonic experience, gradually coupling neurons of the superficial CA1 pyramidale sublayer to whole population activity. Applying hippocampal theta-driven closed-loop optogenetic suppression to mitigate this neuronal recruitment during (food-context) memory formation relaxed the topological constraint on hippocampal coactivity and restored subsequent flexible (object-location) memory. These findings uncover an organizational principle for the peer-to-peer coactivity structure of the hippocampal cell population to successfully meet memory demands.

neuroscience↗