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Mazuski, C.

Publications and source records attributed to Mazuski, C..

6 recordsLinked to original sources

Differential encoding of social identity, valence and unfamiliarity in the amygdala and piriform cortex

To appropriately respond to social situations, animals must rapidly identify conspecifics as individuals, gauge their familiarity and recall any good or bad associations. In previous work (Mazuski & OKeefe, 2022), we characterized populations of neurons in the basolateral amygdala complex (BLA) that were strongly tuned to social conspecifics. In this current study, we asked whether these or other populations in the BLA encode properties necessary for social interaction: individual recognition, familiarity detection and reward association. In addition to cells in the rat lateral amygdala (LA) and basolateral amygdala (BLA), we recorded from cells in the anatomically-related piriform cortex (PIR) to see how much of the amygdala response was inherited from this input. Here, we show that these three interrelated areas encode distinct features of social conspecifics at the population and single neuron level. We recorded from large populations of neurons using 4-shank Neuropixels probes while rats learned a social discrimination task, where one male conspecific was paired with a food reward (S+) and the other its absence (S-). For comparison, two unfamiliar animals were presented on occasional probe trials. After successful discrimination learning, we looked for transfer effects to our previously studied task where implanted rats freely interacted with all four conspecifics in an open-field environment. The LA dynamically encoded social reward learning. Initially, LA neuronal population activity could not distinguish between the S+ and S-conspecifics, but after learning distinct representations emerged. In contrast, the PIR showed no effect of social reward learning. Single PIR units encoded social identity with strong tuning to individual conspecifics both before and after learning. The BLA encoded both reward learning and social identity suggesting this is where the PIR and LA information streams converge. Unexpectedly, the BLA and LA strongly coded for the unfamiliarity of the rat - single neurons responded to the probe trial animals with firing rates 2-5x higher than to the task animals. This cross-region encoding of identity, reward and unfamiliarity was reactivated during social interaction in the new open-field environment, demonstrating that the learning was not context specific. The results throw light on how distinct neural circuits contribute to social recognition and memory and how they interact with each other.

neuroscience↗

Repix: reliable, reusable, versatile chronic Neuropixels implants using minimal components

Neuropixels probes represent the state-of-the-art for high-yield electrophysiology in neuroscience: the simultaneous recording of hundreds of neurons is now routinely carried out in head-restrained animals. In contrast, neural recording in unrestrained animals, as well as recording and tracking neurons over days, remains challenging, though it is possible using chronic implants. A major challenge is the availability of simple methods that can be implemented with limited or no prior experience with Neuropixels probes, while achieving reliable, reusable, versatile high-density electrophysiology. Here we developed, deployed, and evaluated the real-world performance of Repix, a chronic implantation system that permits the repeated re-use of Neuropixels probes. The lightweight system allows implanted animals to express a full range of natural behaviors, including social behaviors. We show that Repix allows the recording of hundreds of neurons across many months, up to a year, with implants across cortical and subcortical brain regions. Probes can be reused repeatedly with stable yield. Repix has been used by 16 researchers in 10 laboratories to date, and we evaluated the real-world performance of Repix in a variety of chronic recording paradigms in both mice and rats with a combined 209 implantations. We found that the key advantage of Repix is robustness and simplicity. Adopters of Repix became proficient at five procedures on average, regardless of prior experience with in vivo electrophysiology. With the companion protocol alongside this article, the performance and user-friendliness of Repix should facilitate a wide uptake of chronic Neuropixels recordings.

neuroscience↗

Basolateral Amygdala Represents and Remembers Ethological Events

The basolateral amygdala plays a crucial role in memory consolidation yet the general neural mechanism remains elusive. Basolateral amygdala neurons were recorded from freely-moving rats as they interacted with different ethological stimuli: male or female rats, a moving toy and food. Over 20% of neurons showed highly tuned event-specific responses to a single class of stimuli. Firing persisted in 30% of these responsive cells for minutes after the removal of the eliciting stimulus. Neural information flowed directionally from event-specific neurons to less specific neurons with changes in connection strength after removal of the stimulus. We propose that the basolateral amygdala identifies specific ethological events, with circuit-wide activity driven by the event-specific neurons during and after the termination of those events likely facilitating active short-term memory consolidation.

neuroscience↗

Adult mice lacking VIP SCN neurons retain circadian locomotor behavior but exhibit dampened daily glucocorticoid rhythms

The suprachiasmatic nucleus (SCN) drives circadian rhythms in locomotion through coupled, single-cell oscillations. Global genetic deletion of the neuropeptide, Vip or its receptor Vipr2, results in profound deficits in daily synchrony among SCN cells and daily rhythms in locomotor behavior and glucocorticoid secretion. To test whether this phenotype depends on VIP neurons in the SCN, we ablated VIP SCN neurons in vivo in adult mice through Caspase3-mediated induction of the apoptotic pathway in cre-expressing VIP neurons. We found that ablation of VIP SCN neurons in adult mice caused a phenotype distinct from Vip- and Vipr2- null mice. Mice lacking VIP neurons retained rhythmic locomotor activity with a shortened circadian period, more variable onsets and decreased duration of daily activity. Circadian hormonal outputs, specifically corticosterone rhythms were severely dampened. In contrast, deletion of neonatal SCN VIP neurons dramatically reduced circadian gene expression in the cultured SCN, mimicking the effects of global deletion of Vip or Vipr2. These results suggest that SCN VIP neurons play a role in lengthening circadian period and stimulating the daily surge in glucocorticoids in adults and in synchronizing and sustaining daily rhythms among cells in the developing SCN. Significance StatementThe importance of the neuropeptide, VIP, for circadian rhythms has been described in mice lacking the gene for Vip or its receptor, Vipr2. This study found that ablation of VIP neurons only in the adult SCN reproduced the loss of circadian rhythms in glucocorticoids, but not the loss of circadian locomotor behavior, seen with global loss of VIP signaling. We conclude that VIP SCN neurons play two roles: one in adulthood lengthening circadian period and regulating circadian outputs, and one in development coordinating synchrony among circadian cells.

neuroscience↗

Entrainment of circadian rhythms depends on firing rates and neuropeptide release of VIP SCN neurons

The mammalian suprachiasmatic nucleus (SCN) functions as a master circadian pacemaker, integrating environmental input to align physiological and behavioral rhythms to local time cues. Approximately 10% of SCN neurons express vasoactive intestinal polypeptide (VIP); however, it is unknown how firing activity of VIP neurons releases VIP to entrain circadian rhythms. To identify physiologically relevant firing patterns, we optically tagged VIP neurons and characterized spontaneous firing over three days. VIP neurons had circadian rhythms in firing rate and exhibited two classes of instantaneous firing activity. We next tested whether physiologically relevant firing affected circadian rhythms through VIP release. We found that VIP neuron stimulation with high, but not low, frequencies shifted gene expression rhythms in vitro through VIP signaling. In vivo, high frequency VIP neuron activation rapidly entrained circadian locomotor rhythms. Thus, increases in VIP neuronal firing frequency release VIP and entrain molecular and behavioral circadian rhythms.\n\nHighlightsO_LIMazuski et al. identified three classes of circadian SCN neurons based on their distinct firing patterns consistent over multiple days\nC_LIO_LIThere are two distinct classes (tonic and irregular firing) of VIP SCN neurons.\nC_LIO_LIStimulation of VIP SCN neurons at physiologically relevant frequencies phase shifts whole-SCN circadian rhythms in gene expression through VIP release. These effects are blocked with VIP antagonists.\nC_LIO_LIFiring of VIP SCN neurons entrains circadian rhythms in locomotor behavior in a frequency and time-of-day dependent manner.\nC_LI

neuroscience↗

Neuronal tracing and analysis by multispectral tracing in densely labeled mouse brain

Accurate and complete neuronal wiring diagrams are necessary for understanding brain function at many scales from long-range interregional projections to microcircuits. Traditionally, light microscopy-based anatomical reconstructions use monochromatic labeling and therefore necessitate sparse labeling to eliminate tracing ambiguity between intermingled neurons. Consequently, our knowledge of neuronal morphology has largely been based on averaged estimations across many samples. Recently developed second-generation Brainbow tools promise to circumvent this limitation by revealing fine anatomical details of many unambiguously identifiable neurons in densely labeled samples. Yet, a means to quantify and analyze the information is currently lacking. Therefore, we developed nTracer, an ImageJ plugin capable of rapidly and accurately reconstructing whole-cell morphology of large neuronal populations in densely labeled brains.

neuroscience↗