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Julian, J. B.

Publications and source records attributed to Julian, J. B..

3 recordsLinked to original sources

Hippocampal engrams configure prefrontal context representations to guide flexible decisions

Flexible behavior requires using past experiences to configure cortical computations to suit current task demands. A central question in neuroscience is how memory representations control such reconfigurations. Although hippocampal (HPC) engrams can drive learned behaviors, prior studies have been largely limited to a fixed stimulus-response computation. Thus, whether engrams can drive retrieval of a set of stimulus-response mappings, rather than a specific response itself, remains unresolved. Moreover, how engrams affect cortical task representations and dynamics so as to produce engram-consistent behavior remains unstudied. Here, we address both questions by combining tagging and reactivation of HPC engrams with simultaneous large-scale recordings in medial prefrontal cortex (mPFC) during a context-dependent task-switching paradigm in mice. We report that HPC engram reactivation caused mice to apply engram-consistent decision-rules rather than a specific motor output. Simultaneous mPFC recordings revealed that reactivating the HPC engram for a given context reinstated the representation of that context in mPFC within hundreds of milliseconds, indicating that it was mediated by rapid network effects, leading to choice behavior consistent with the reactivated HPC engram. Other aspects of endogenous dynamics in mPFC were left remarkably intact. Together, our findings provide direct causal evidence that HPC engrams can configure task-relevant population states of downstream cortical circuits in real time, establishing a neural mechanism by which memory traces control flexible behavior.

neuroscience↗

Neural compass in the human brain during naturalistic virtual navigation

A central component of wayfinding is the ability to maintain a consistent representation of ones facing direction when moving about the world. In rodents, head direction cells are believed to support this "neural compass", but identifying a similar mechanism in humans during dynamic naturalistic navigation has been challenging. To address this issue, we acquired fMRI data while participants freely navigated through a virtual reality city. Encoding model analyses revealed voxel clusters in retrosplenial complex and superior parietal lobule that exhibited reliable tuning as a function of facing direction. Crucially, these directional tunings were consistent across perceptually different versions of the city, spatially separated locations within the city, and motivationally distinct phases of the behavioral task. Analysis of the model weights indicated that these regions may represent facing direction relative to the principal axis of the environment. These findings reveal specific mechanisms in the human brain that allow us to maintain a sense of direction during naturalistic, dynamic navigation.

neuroscience↗

Manipulation of neuronal activity in the entorhinal-hippocampal circuit affects intraneuronal amyloid-β levels

One of the neuropathological hallmarks of Alzheimers disease (AD) is the accumulation of amyloid-{beta} (A{beta}) plaques, which is preceded by intraneuronal build-up of toxic, aggregated A{beta} during disease progression. A{beta} plaques are first deposited in the neocortex before appearing in the medial temporal lobe, and tau pathology with subsequent neurodegeneration in the latter anatomical region causes early memory impairments in patients. Current research suggests that early intraneuronal A{beta} build-up may begin in superficial layers of lateral entorhinal cortex (LEC). To examine whether manipulation of neuronal activity of LEC layer II neurons affected intraneuronal A{beta} levels in LEC and in downstream perforant path terminals in the hippocampus (HPC), we used a chemogenetic approach to selectively and chronically silence superficial LEC neurons in young and aged 3xTg AD mice and monitored its effect on intraneuronal A{beta} levels in LEC and HPC. Chronic chemogenetic silencing of LEC neurons led to reduced early intraneuronal A{beta} in LEC and in projection terminals in the HPC, compared with controls. Early intraneuronal A{beta} levels in the downstream HPC correlated with activity levels in superficial layers of LEC, with the subiculum being the earliest subregion involved, and our findings give evidence to early AD neuropathology originating in select neuronal populations.

neuroscience↗