bioRxiv Science⌕ Search

Biology subjects

Le Merre, P.

Publications and source records attributed to Le Merre, P..

3 recordsLinked to original sources

Capturing Spatially Organized Oscillatory Cliques as Signatures of Neuronal Assemblies

State-of-the-art neural recording technologies now enable dense sampling of neuronal activity, demonstrating meaningful spiking variability from moment to moment. Yet spiking activity is sparse by nature and allows only partial access to collective neuronal dynamics. Local field potentials (LFPs) provide complementary information by capturing coordinated activity from large neuronal populations, but methods to characterize the fine-scale spatio-temporal organization of LFPs are lacking. Starting from the notion that neural oscillations are brief and burst-like, we introduce a framework to detect and analyze SPatially Organized Oscillatory Cliques (SPOOCs), oscillatory events that are cohesive in space, time, and frequency. SPOOCs displayed diverse dynamics in space and frequency and were differentially modulated during stimulus processing. Linking SPOOCs to local spiking, we demonstrate that these events index rapid reconfigurations of neuronal assemblies. With SPOOChunter, we provide an open-source toolbox that enables systematic detection and analysis of transient, spatially organized population dynamics in high-density electrophysiological recordings.

neuroscience↗

A Prefrontal Cortex Map based on Single Neuron Activity

The intrinsic organization underlying the central cognitive role of the prefrontal cortex (PFC) is poorly understood. The work to date has been dominated by cytoarchitecture as a canvas for studies on the PFC, constraining concepts, analyses, results, and their interpretations to pre-configured delimitations that might not be relevant to function. We approached organization by profiling the activity and spatial location of >23,000 neurons recorded in awake mice. Regularly firing neurons were over-represented in most PFC subregions, yet a fine-grained activity map of the PFC did not align with cytoarchitecturally defined subregions. Instead, we observed a robust relationship between spontaneous activity patterns and intra-PFC hierarchy, suggesting internal organization principles transcending cytoarchitecture. Single neuron responses to sounds did not reflect intra-PFC hierarchy but were linked to spontaneous firing rate, indicating that responsiveness increases with excitability and is decoupled from the PFCs intrinsic operational structure. Our data-driven approach provides a scalable roadmap to explore functional organizations in diverse brain regions and species, opening avenues to link activity, structure, and function in the brain.

neuroscience↗

Esr1+ hypothalamic-habenula neurons shape aversive states.

Excitatory projections from the lateral hypothalamic area (LHA) to the lateral habenula (LHb) drive aversive responses. We used Patch-seq guided multimodal classification to define the structural and functional heterogeneity of the LHA-LHb pathway. Our classification identified six glutamatergic neuron types with unique electrophysiological properties, molecular profiles, and projection patterns. We found that genetically-defined LHA-LHb neurons signal distinct aspects of emotional or naturalistic behaviors: Esr1+ LHA-LHb neurons induce aversion, whereas Npy+ LHA-LHb neurons control rearing behavior. Repeated optogenetic drive of Esr1+ LHA-LHb neurons induces a behaviorally persistent aversive state, and large-scale recordings showed a region-specific neural representation of the aversive state in the prelimbic region of the prefrontal cortex. We further found that exposure to unpredictable mild shocks induced a sex-specific sensitivity to develop a stress state in female mice, which was associated with a specific shift in the intrinsic properties of bursting-type Esr1+ LHA-LHb neurons. In summary, we describe the diversity of LHA-LHb neuron types, and provide evidence for the role of Esr1+ neurons in aversion and sexually dimorphic stress sensitivity.

neuroscience↗