Understanding the neuronal substrates of flexible visual processing in everyday life

BBSRC · United Kingdom government procurement

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September 29, 2027
Response Due
Active
Status

Opportunity Overview

"Visual processing has mostly been studied in static conditions in which subjects (humans or animal models) do not move. While in these conditions the basic elements of visual processing have been established, we know surprisingly little about visual processing in more natural conditions, in which the subjects move around their natural environments.

Over the last decade studies in rodents, fishes, flies and humans provided robust evidence indicating that motor actions have major effects on neural activity in the visual system and indicating that visual processing is heavily controlled by the behavioral state of the subject. This new scenario is consistent with anatomical data indicating that only a small fraction of synaptic inputs to visual thalamus comes from the retina, while the rest is constituted by projections from cortex and other thalamic and brainstem nuclei. We currently have a good understanding of the retinal projections, but we know little about all the non-retinal projections that modulate visual processing according to behavioural states."
Our research aims to address these major gaps in our understanding of visual processing in natural, real-life conditions. More specifically we address four questions:

1) What informations about behavioural state are conveyed to the visual thalamus?
2) How informations about behavioural states are integrated with the incoming visual information? What is the effect of such integration on visual processing?
3) What is the source of these information? Which brain areas provide which type of information?
4) How and to what extent behavioural information in visual thalamus affects action selection in subsequent behaviors?

To do that, we will take advantage of our ability to measure 3D motor actions in freely behaving animals [1], combined with simultaneous brain recordings (as in [2] but from high-throughput ~1000 channel Neuropixel electrodes [3]) and optogenetic stimulation of well-defined cell types. The...

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Solicitation Details

Issuing agencyBBSRC
CountryUnited Kingdom
CategoryResearch Development
PublishedSeptember 30, 2023
Procurement stageActive solicitation
Response dueSeptember 29, 2027
StatusOpen — accepting responses
Official sourceView original notice
Last verifiedOctober 06, 2026

Source: UK Research and Innovation (UKRI) — Open Government Licence v3.0.

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