4.8 Article

Visual exposure enhances stimulus encoding and persistence in primary cortex

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2105276118

Keywords

visual exposure; stimulus persistence; primary visual cortex; self-organization

Funding

  1. Deutsche Forschungs-Gemeinschaft (DFG) [NI708/5-1, SPP 1665]
  2. European Union (EU) [FP7-604 102-HBP]
  3. Reinhart Kosselleck grant of the German Research Foundation
  4. EU's 7th Framework Programme (FP7/2007-2013 Neuroseeker)

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The study shows that brief exposure to structured visual stimuli can enhance stimulus encoding in the primary visual cortex of cats, increasing the range of neuronal responses and segregating them into stimulus-specific clusters. These refinements in neuronal responses observed post-exposure preserve representational details necessary for stimulus reconstruction and can potentially benefit simple readouts at higher stages of visual processing.
The brain adapts to the sensory environment. For example, simple sensory exposure can modify the response properties of early sensory neurons. How these changes affect the overall encoding and maintenance of stimulus information across neuronal populations remains unclear. We perform parallel recordings in the primary visual cortex of anesthetized cats and find that brief, repetitive exposure to structured visual stimuli enhances stimulus encoding by decreasing the selectivity and increasing the range of the neuronal responses that persist after stimulus presentation. Lowdimensional projection methods and simple classifiers demonstrate that visual exposure increases the segregation of persistent neuronal population responses into stimulus-specific clusters. These observed refinements preserve the representational details required for stimulus reconstruction and are detectable in postexposure spontaneous activity. Assuming response facilitation and recurrent network interactions as the core mechanisms underlying stimulus persistence, we show that the exposure-driven segregation of stimulus responses can arise through strictly local plasticity mechanisms, also in the absence of firing rate changes. Our findings provide evidence for the existence of an automatic, unguided optimization process that enhances the encoding power of neuronal populations in early visual cortex, thus potentially benefiting simple readouts at higher stages of visual processing.

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