ArticlePLoS computational biology2025
Cell-type-specific firing patterns in a V1 cortical column model depend on feedforward and feedback-driven states.
Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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7 citing papers in PubMed.
- Resting-state EEG alpha-BOLD coupling spatially follows cortical cell-type and receptor gradients.bioRxiv : the preprint server for biology · 2026Article
- Diverse and flexible behavioral strategies arise in recurrent neural networks trained on multisensory decision making.PLoS computational biology · 2025Article
- Cortical networks with multiple interneuron types generate oscillatory patterns during predictive coding.PLoS computational biology · 2025Article
- A simplified model of NMDA-receptor-mediated dynamics in leaky integrate-and-fire neurons.Journal of computational neuroscience · 2025Article
- Adaptive arousal regulation: Pharmacologically shifting the peak of the Yerkes-Dodson curve by catecholaminergic enhancement of arousal.Proceedings of the National Academy of Sciences of the United States of America · 2025Article
- Synaptic plasticity facilitates oscillations in a V1 cortical column model with multiple interneuron types.Frontiers in computational neuroscience · 2025Article
- Functional connectivity drifts during sleep as a marker of fluctuations in the level of consciousness.Neuroscience of consciousness · 2025Article
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4 authors.
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Abstract
Stimulation of specific cell groups under different network regimes (e.g., spontaneous activity or sensory-evoked activity) can provide insights into the neural dynamics of cortical columns. While these protocols are challenging to perform experimentally, modelling can serve as a powerful tool for such explorations. Using detailed electrophysiological and anatomical data from mouse V1, we built a novel spiking network model of a cortical column, which incorporates pyramidal cells and three distinct interneuron types (PV, SST, and VIP cells, specified per lamina), as well as the dynamic and voltage-dependent properties of AMPA, GABA, and NMDA receptors. We first demonstrate that thalamocortical feedforward (FF) and feedback (FB) stimuli arriving in the column have opposite effects, leading to net columnar excitation and inhibition respectively and revealing translaminar gain control via full-column inhibition by layer 6. We then perturb one cell group (i.e., a cell type in a specific layer) at a time and observe the effects on other cell groups under distinct network states: spontaneous, feedforward-driven, feedback-driven, and a combination of feedforward and feedback. Our findings reveal that when a given group is perturbed, the columnar response varies significantly based on its state, with strong sensory feedforward input decreasing columnar sensitivity to all perturbations and feedback input serving as modulator of intra columnar interactions. Given that activity changes within specific neuronal populations are difficult to predict a priori in experiments, our model may constitute a useful tool to predict outcomes of perturbations and assist in experimental design.
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