Unexpected events modulate context signaling in VIP and excitatory cells of the visual cortex

Abstract

The visual cortex predicts incoming sensory stimuli through internal models of the world. Unexpected stimuli that violate these predictions update internal models and drive adaptation. Cortical inhibitory neurons, particularly VIP (vasoactive intestinal peptide) interneurons, are suggested to play a key role in representing unexpected stimuli, given their robust firing following unexpected omissions of familiar images. Importantly, this response is stimulus non-specific, raising an important question about what information it conveys. Given their unique connectivity with other cell types and brain areas, we hypothesized that during unexpected events, VIP neurons encode contextual information, defined as neuronal activity that is not driven by the stimulus itself. To test this hypothesis, we analyzed the Allen Institute Visual Behavior dataset, in which mice viewed repeated familiar images and unexpected omissions of these images while two-photon calcium imaging data from different cell types and visual areas were recorded. Using dimensionality reduction techniques, we found that omissions trigger contextual signaling in VIP neurons in the primary visual cortex (V1) and the lateral medial (LM) visual area, particularly in the superficial layers. Similarly, contextual coding was enhanced in excitatory neurons following omissions. This contrasted sharply with the excitatory response to expected images, during which contextual information was substantially suppressed. Our results suggest that unexpected events activate VIP neurons, which subsequently propagate contextual information across the cortical network. This potentially facilitates the integration of context within the cortical network, and leads to updated predictions about our dynamic environment.