Contextual modulation emerges by integrating feedforward and feedback processing in mouse visual cortex

Sensory systems use context to infer meaning. Accordingly, context profoundly influences neural responses to sensory stimuli. However, a cohesive understanding of the circuit mechanisms governing contextual effects across different stimulus conditions is still lacking. Here we present a unified circuit model of mouse visual cortex that accounts for the main standard forms of contextual modulation. This data-driven and biologically realistic circuit, including three primary inhibitory cell types, sheds light on how bottom-up, top-down, and recurrent inputs are integrated across retinotopic space to generate contextual effects in layer 2/3. We establish causal relationships between neural responses, geometrical features of the inputs, and the connectivity patterns. The model not only reveals how a single canonical cortical circuit differently modulates sensory response depending on context but also generates multiple testable predictions, offering insights that apply to broader neural circuitry.

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Publication Details

Journal
Cell Reports
Published
2024-12-20
DOI
https://doi.org/10.1016/j.celrep.2024.115088
Citations
7
Primary Topic
Neural dynamics and brain function
Type
article
Field-Weighted Citation Impact
2.40

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article

Contextual modulation emerges by integrating feedforward and feedback processing in mouse visual cortex

Mario Dipoppa, Massimo Scanziani, Serena Di Santo, Morgane Roth et al.
7 citations
Cell Reports
Neural dynamics and brain function
2.40
article

Contextual modulation emerges by integrating feedforward and feedback processing in mouse visual cortex

Mario Dipoppa, Massimo Scanziani, Serena Di Santo, Morgane Roth, Andreas Keller, Kenneth D. Miller
article en
7 citations

Abstract

Sensory systems use context to infer meaning. Accordingly, context profoundly influences neural responses to sensory stimuli. However, a cohesive understanding of the circuit mechanisms governing contextual effects across different stimulus conditions is still lacking. Here we present a unified circuit model of mouse visual cortex that accounts for the main standard forms of contextual modulation. This data-driven and biologically realistic circuit, including three primary inhibitory cell types, sheds light on how bottom-up, top-down, and recurrent inputs are integrated across retinotopic space to generate contextual effects in layer 2/3. We establish causal relationships between neural responses, geometrical features of the inputs, and the connectivity patterns. The model not only reveals how a single canonical cortical circuit differently modulates sensory response depending on context but also generates multiple testable predictions, offering insights that apply to broader neural circuitry.

Cell ReportsVol. 44(1)
Allen Institute for Brain Science (US), Howard Hughes Medical Institute (US), Universidad de Granada (ES), University of California, San Francisco (US), University of California San Francisco Medical Center (US)
National Science Foundation, Foundation for the National Institutes of Health, Gatsby Charitable Foundation, European Commission, National Institutes of Health, Agencia Estatal de Investigación, Spanish National Plan for Scientific and Technical Research and Innovation
Openalex Percentile: Top 11%
Neural dynamics and brain function
2.40
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