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Wiener, S.

Publications and source records attributed to Wiener, S..

3 recordsLinked to original sources

Identification of Synchronously Active Cells (ISAC) to study the activity of cell assemblies

Cell assemblies--groups of neurons that fire synchronously--are central to neuronal computation. Technological advances now permit the simultaneous recording of large neuronal populations; however, many existing cell assembly detection algorithms rely on simplified measures such as pairwise correlations, failing to capture higher-order synchrony and thereby missing a rich repertoire of assemblies present in the data. To address these limitations, we developed Identification of Synchronously Active Cells (ISAC), which performs a rigorous, iterative search across all recorded units, leveraging the full dimensionality of the dataset to detect groups that fire together above chance. Using simulated recordings with ground-truth assemblies of increasing complexity, we demonstrate that ISAC considerably outperforms currently used algorithms in identifying synchronously active cells. Finally, we show that applying ISAC to experimental recordings uncovers novel features of assembly formation and dynamics. The power and sensitivity of ISAC can thus enable insights that remain inaccessible with existing methods.

neuroscience↗

Rhythmic oscillations in the midbrain dopaminergic nuclei in mice

Dopamine release in the forebrain by midbrain ventral tegmental nucleus (VTA) and substantia nigra pars compacta (SNpc) neurons is implicated in reward processing, goal-directed learning, and decision-making. Rhythmic oscillations of neural excitability underlie coordination of network processing, and have been reported in these dopaminergic nuclei at several frequency bands. This paper provides a comparative characterization of several frequencies of oscillations of local field potential and single unit activity, highlighting some behavioral correlates. We recorded from optogenetically identified dopaminergic sites in mice training in operant olfactory and visual discrimination tasks. Rayleigh and Pairwise Phase Consistency (PPC) analyses revealed some VTA/SNc neurons phase-locked to each frequency range, with fast spiking interneurons (FSIs) prevalent at 1-2.5 Hz (slow) and 4 Hz bands, and dopaminergic neurons predominant in the theta band. More FSIs than dopaminergic neurons were phase-locked in the slow and 4 Hz bands during many task events. The highest incidence of phase-locking in neurons was in the slow and 4 Hz bands, and occurred during the delay between the operant choice and trial outcome (reward or punishment) signals. These data provide a basis for further examination of rhythmic coordination of activity of dopaminergic nuclei with other brain structures, and its impact for adaptive behavior.

neuroscience↗

Flexible communication between cell assemblies and 'reader' neurons

Cell assemblies are considered fundamental units of brain activity, underlying diverse functions ranging from perception to memory and decision-making. Cell assemblies have generally been studied in relation to specific stimuli or actions, but this approach does not readily extend to more abstract constructs. An alternative approach is to assess cell assemblies without making reference to external variables, and instead focus on internal brain processes -- by defining assemblies by their endogenous ability to effectively elicit specific responses in downstream ( reader) neurons. However, this compelling idea currently lacks experimental support. Here, we provide evidence for assembly-reader communication. Reader activation was genuinely collective, functionally selective, yet flexible, implementing both pattern separation and completion. These processes occurred at the time scale of membrane integration, synaptic plasticity and gamma oscillations. Finally, assembly-reader couplings were selectively modified upon associative learning, indicating that they were plastic and could become bound to behaviorally relevant variables. These results support cell assemblies as an endogenous mechanism for brain function.

neuroscience↗