Functional clustering drives encoding improvement in a developing brain network during awake visual learning.

Sensory experience drives dramatic structural and functional plasticity in developing neurons. However, for single-neuron plasticity to optimally improve whole-network encoding of sensory information, changes must be coordinated between neurons to ensure a full range of stimuli is efficiently repres...

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Main Authors: Kaspar Podgorski, Derek Dunfield, Kurt Haas
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Biology
Online Access:http://europepmc.org/articles/PMC3254648?pdf=render
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author Kaspar Podgorski
Derek Dunfield
Kurt Haas
author_facet Kaspar Podgorski
Derek Dunfield
Kurt Haas
author_sort Kaspar Podgorski
collection DOAJ
description Sensory experience drives dramatic structural and functional plasticity in developing neurons. However, for single-neuron plasticity to optimally improve whole-network encoding of sensory information, changes must be coordinated between neurons to ensure a full range of stimuli is efficiently represented. Using two-photon calcium imaging to monitor evoked activity in over 100 neurons simultaneously, we investigate network-level changes in the developing Xenopus laevis tectum during visual training with motion stimuli. Training causes stimulus-specific changes in neuronal responses and interactions, resulting in improved population encoding. This plasticity is spatially structured, increasing tuning curve similarity and interactions among nearby neurons, and decreasing interactions among distant neurons. Training does not improve encoding by single clusters of similarly responding neurons, but improves encoding across clusters, indicating coordinated plasticity across the network. NMDA receptor blockade prevents coordinated plasticity, reduces clustering, and abolishes whole-network encoding improvement. We conclude that NMDA receptors support experience-dependent network self-organization, allowing efficient population coding of a diverse range of stimuli.
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spelling doaj.art-84f540209ed14584b065fb45fdb60d842022-12-21T21:32:12ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852012-01-01101e100123610.1371/journal.pbio.1001236Functional clustering drives encoding improvement in a developing brain network during awake visual learning.Kaspar PodgorskiDerek DunfieldKurt HaasSensory experience drives dramatic structural and functional plasticity in developing neurons. However, for single-neuron plasticity to optimally improve whole-network encoding of sensory information, changes must be coordinated between neurons to ensure a full range of stimuli is efficiently represented. Using two-photon calcium imaging to monitor evoked activity in over 100 neurons simultaneously, we investigate network-level changes in the developing Xenopus laevis tectum during visual training with motion stimuli. Training causes stimulus-specific changes in neuronal responses and interactions, resulting in improved population encoding. This plasticity is spatially structured, increasing tuning curve similarity and interactions among nearby neurons, and decreasing interactions among distant neurons. Training does not improve encoding by single clusters of similarly responding neurons, but improves encoding across clusters, indicating coordinated plasticity across the network. NMDA receptor blockade prevents coordinated plasticity, reduces clustering, and abolishes whole-network encoding improvement. We conclude that NMDA receptors support experience-dependent network self-organization, allowing efficient population coding of a diverse range of stimuli.http://europepmc.org/articles/PMC3254648?pdf=render
spellingShingle Kaspar Podgorski
Derek Dunfield
Kurt Haas
Functional clustering drives encoding improvement in a developing brain network during awake visual learning.
PLoS Biology
title Functional clustering drives encoding improvement in a developing brain network during awake visual learning.
title_full Functional clustering drives encoding improvement in a developing brain network during awake visual learning.
title_fullStr Functional clustering drives encoding improvement in a developing brain network during awake visual learning.
title_full_unstemmed Functional clustering drives encoding improvement in a developing brain network during awake visual learning.
title_short Functional clustering drives encoding improvement in a developing brain network during awake visual learning.
title_sort functional clustering drives encoding improvement in a developing brain network during awake visual learning
url http://europepmc.org/articles/PMC3254648?pdf=render
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