Journal
JOURNAL OF NEUROSCIENCE
Volume 41, Issue 18, Pages 3988-4005Publisher
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.1895-20.2021
Keywords
context dependence; gain modulation; locomotion; sensory cortex; spiking networks; visual processing
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Funding
- National Institute of Deafness and Other Communication Disorders Grant [K25-DC013557]
- National Institute of Neurological Disorders and Stroke Grant [NS118461]
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To thrive in dynamic environments, animals must be capable of rapidly and flexibly adapting behavioral responses to changing context and internal state. Our theoretical framework classifies the effects of cell type-specific top-down perturbations on the information processing speed of cortical circuits, demonstrating that perturbation effects on stimulus processing can be predicted by intrinsic gain modulation. This theory leads to counterintuitive effects, such as improved performance with increased input variance, linking connectivity, dynamics, and information processing via gain modulation.
To thrive in dynamic environments, animals must be capable of rapidly and flexibly adapting behavioral responses to changing context and internal state. Examples of behavioral flexibility include faster stimulus responses when attentive and slower responses when distracted. Contextual or state-dependent modulations may occur early in the cortical hierarchy and may be implemented via top-down projections from corticocortical or neuromodulatory pathways. However, the computational mechanisms mediating the effects of such projections are not known. Here, we introduce a theoretical framework to classify the effects of cell type-specific top-down perturbations on the information processing speed of cortical circuits. Our theory demonstrates that perturbation effects on stimulus processing can be predicted by intrinsic gain modulation, which controls the timescale of the circuit dynamics. Our theory leads to counterintuitive effects, such as improved performance with increased input variance. We tested the model predictions using large-scale electrophysiological recordings from the visual hierarchy in freely running mice, where we found that a decrease in single-cell intrinsic gain during locomotion led to an acceleration of visual processing. Our results establish a novel theory of cell type-specific perturbations, applicable to top down modulation as well as optogenetic and pharmacological manipulations. Our theory links connectivity, dynamics, and information processing via gain modulation.
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