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Grover, D.

Publications and source records attributed to Grover, D..

2 recordsLinked to original sources

Multi-timescale learning signals in Drosophila dopaminergic neurons

Learning often requires inference over hidden task structure, including features that predict outcomes. In mammals, prediction-error signaling by midbrain dopamine neurons is considered central to learning, but how these neurons reflect the progression and stability of learning remains unclear. Using Drosophila to monitor calcium activity at trial-by-trial resolution during aversive conditioning, we found that PPM3 dopaminergic neurons exhibit hallmark prediction-error responses in which activity shifted from the unconditioned stimulus (US) to the conditioned stimulus (CS), was suppressed when an expected US was omitted, and increased when the US exceeded expectations. Strikingly, the same neurons also exhibited slower state-like dynamics across trials, including tonic activity transitions that emerged with learning and tracked the acquisition of learned behavior, and perturbation-related dynamics that were briefly disrupted when expectations were violated. Increasing task demands by inserting a temporal gap between the CS and US (trace conditioning) delayed both response types to later trials, accompanied by corresponding delays in behavior acquisition. In addition, dopaminergic activity developed an anticipatory response that tracked the expected timing of the US during the gap. These findings reveal that a single dopaminergic neuron type integrates moment-to-moment prediction errors, expected outcome timing, and a longer-timescale signal reflecting learning stabilization, establishing Drosophila as a bona fide model for dissecting the neural mechanisms that shape learning under changing task demands.

neuroscience↗

Inhibitory-modulatory coupling generates persistent activity during working memory

Working memory requires the stable maintenance of neural representations across temporal gaps, yet the circuit mechanisms that generate and stabilize persistent activity remain unsolved. Prevailing models emphasize recurrent excitation as the principal substrate of persistence, but how inhibitory and modulatory interactions shape the stability of temporal dynamics is unclear. Here, using trace conditioning in Drosophila, a working memory-dependent form of associative learning, we identify reciprocal inhibition as a circuit mechanism for sustaining persistent activity. In trace conditioning, a "trace" interval separates the conditioned and unconditioned stimuli, requiring maintenance of a neural representation across the trace interval, to support learning. Combining virtual-reality behavior, targeted neurogenetic perturbations, in vivo two-photon calcium imaging, and real-time neurotransmitter measurements, we uncover a reciprocal inhibitory microcircuit within the ellipsoid body that is selectively engaged during trace, but not delay (overlapping CS-US), conditioning. During the trace interval, ER2/4m neurons exhibit sustained activity, while reciprocally connected ER3/4d neurons show progressively strengthened suppression, forming a dynamically stabilized inhibitory loop. Disrupting GABA synthesis or reception within this circuit abolishes persistent activity and impairs trace learning, demonstrating the causal requirement for reciprocal inhibition in working memory maintenance. We further show that glutamatergic and nitric oxide signaling enhance inhibitory efficacy during the trace interval. In vivo neurotransmitter imaging reveals temporally structured dynamics in which glutamatergic signaling precedes and amplifies sustained GABAergic inhibition, consistent with modulatory stabilization of circuit persistence. Together, these findings identify reciprocal inhibition, reinforced by modulatory signaling, as a core circuit mechanism for dynamically stabilizing persistent neural representations. Our results challenge excitation-centric models of working memory and establish inhibitory-modulatory loops as a fundamental substrate for maintaining memory traces across time.

neuroscience↗