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McCarthy, P. T.

Publications and source records attributed to McCarthy, P. T..

2 recordsLinked to original sources

Cell-type-specific cortical feedback coordinates hierarchical credit assignment

Learning is thought to arise from synaptic modifications across brain-wide circuits, yet how these networks coordinate plasticity to support complex behaviour is not known. Inspired by deep learning, we introduce a theory of hierarchical credit assignment in which pathway-specific cortical feedback drives dendrite-dependent burst plasticity across the cortex. We show that this principle enables learning in dynamic settings, complex visual recognition, and goal-directed tasks, mechanistically linking credit assignment to cell-type-specific regulation of dendritic excitation-inhibition balance. Our framework provides a unified account of diverse experimental phenomena -- including cell-type-specific modulation of synaptic plasticity, learning-dependent changes in interneurons, and neuron-specific dendritic error signals. Furthermore, the theory predicts that interneurons constrain the dimensionality of error feedback, offering a functional rationale for cortex-wide gradients in interneuron density. Together, these findings reveal how distinct cortical cell types cooperatively coordinate learning, bridging the gap between synaptic plasticity, circuit-level computation, and behaviour.

neuroscience↗

A transition-prone brain state precedes spontaneous behavioral switching

Animals exhibit behavior in the absence of external stimuli or explicit tasks. Is the initiation of such spontaneous behavior shaped by internal brain states in a predictable manner? If so, does it engage specific brain circuits independent of behavioral form? Here, we studied the initiation of uninstructed behaviors of head-fixed mice in two contexts: a virtual burrow and a running wheel. Across both contexts, mice spent most of the time in quiet wakefulness and spontaneously initiated bouts of egress (exiting the burrow), running, or grooming. We employed functional ultrasound imaging (fUS) to record whole-brain activity and to identify whether the initiation of spontaneous behavior could be predicted from hemodynamic signals. We first identified distinct hemodynamic patterns associated with each behavior and subsequently performed time-resolved decoding to predict behavioral transitions from fUS data. We found that whole-brain hemodynamic signals could decode spontaneous egress and running around 10 seconds before their onset, a timescale that cannot be accounted for by preceding behavioral changes alone. Furthermore, we found a network of regions, including the medial septum (MS), that decreased their signal several seconds before the onset of egress and running. Mimicking this decrease by inhibiting neurons in the MS via optogenetics increased the probability of egress, running, and grooming. Through this unbiased approach, our work sheds light on a whole-brain transition-prone state that precedes uninstructed behavior transitions.

neuroscience↗