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Feature selectivity can explain mismatch signals in mouse visual cortex.

ABSTRACT: Sensory experience often depends on one's own actions, including self-motion. Theories of predictive coding postulate that actions are regulated by calculating prediction error, which is the difference between sensory experience and expectation based on self-generated actions. Signals consistent with prediction error have been reported in the mouse visual cortex (V1) when visual flow coupled to running was unexpectedly stopped. Here, we show that such signals can be elicited by visual stimuli uncoupled to an animal running. We record V1 neurons while presenting drifting gratings that unexpectedly stop. We find strong responses to visual perturbations, which are enhanced during running. Perturbation responses are strongest in the preferred orientation of individual neurons, and perturbation-responsive neurons are more likely to prefer slow visual speeds. Our results indicate that prediction error signals can be explained by the convergence of known motor and sensory signals, providing a purely sensory and motor explanation for purported mismatch signals.

SUBMITTER: Muzzu T

PROVIDER: S-EPMC8655498 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature

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Feature selectivity can explain mismatch signals in mouse visual cortex.

Muzzu Tomaso T Saleem Aman B AB

Cell reports 20211001 1

Sensory experience often depends on one's own actions, including self-motion. Theories of predictive coding postulate that actions are regulated by calculating prediction error, which is the difference between sensory experience and expectation based on self-generated actions. Signals consistent with prediction error have been reported in the mouse visual cortex (V1) when visual flow coupled to running was unexpectedly stopped. Here, we show that such signals can be elicited by visual stimuli un ...[more]

PMID: 34610298

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Project description:Local excitatory connections in mouse primary visual cortex (V1) are stronger and more prevalent between neurons that share similar functional response features. However, the details of how functional rules for local connectivity shape neuronal responses in V1 remain unknown. We hypothesised that complex responses to visual stimuli may arise as a consequence of rules for selective excitatory connectivity within the local network in the superficial layers of mouse V1. In mouse V1 many neurons respond to overlapping grating stimuli (plaid stimuli) with highly selective and facilitatory responses, which are not simply predicted by responses to single gratings presented alone. This complexity is surprising, since excitatory neurons in V1 are considered to be mainly tuned to single preferred orientations. Here we examined the consequences for visual processing of two alternative connectivity schemes: in the first case, local connections are aligned with visual properties inherited from feedforward input (a 'like-to-like' scheme specifically connecting neurons that share similar preferred orientations); in the second case, local connections group neurons into excitatory subnetworks that combine and amplify multiple feedforward visual properties (a 'feature binding' scheme). By comparing predictions from large scale computational models with in vivo recordings of visual representations in mouse V1, we found that responses to plaid stimuli were best explained by assuming feature binding connectivity. Unlike under the like-to-like scheme, selective amplification within feature-binding excitatory subnetworks replicated experimentally observed facilitatory responses to plaid stimuli; explained selective plaid responses not predicted by grating selectivity; and was consistent with broad anatomical selectivity observed in mouse V1. Our results show that visual feature binding can occur through local recurrent mechanisms without requiring feedforward convergence, and that such a mechanism is consistent with visual responses and cortical anatomy in mouse V1.

Dataset Information

Feature selectivity can explain mismatch signals in mouse visual cortex.

Publications

Feature selectivity can explain mismatch signals in mouse visual cortex.

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