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An NMDA receptor-dependent mechanism for subcellular segregation of sensory inputs in the tadpole optic tectum

In the vertebrate CNS, afferent sensory inputs are targeted to specific depths or layers of their target neuropil. This patterning exists ab initio, from the very beginning, and therefore has been considered an activity-independent process. However, here we report that, during circuit development, t...

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Autores principales: Hamodi, Ali S, Liu, Zhenyu, Pratt, Kara G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5135393/
https://www.ncbi.nlm.nih.gov/pubmed/27879199
http://dx.doi.org/10.7554/eLife.20502
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author Hamodi, Ali S
Liu, Zhenyu
Pratt, Kara G
author_facet Hamodi, Ali S
Liu, Zhenyu
Pratt, Kara G
author_sort Hamodi, Ali S
collection PubMed
description In the vertebrate CNS, afferent sensory inputs are targeted to specific depths or layers of their target neuropil. This patterning exists ab initio, from the very beginning, and therefore has been considered an activity-independent process. However, here we report that, during circuit development, the subcellular segregation of the visual and mechanosensory inputs to specific regions of tectal neuron dendrites in the tadpole optic tectum requires NMDA receptor activity. Blocking NMDARs during the formation of these sensory circuits, or removing the visual set of inputs, leads to less defined segregation, and suggests a correlation-based mechanism in which correlated inputs wire to common regions of dendrites. This can account for how two sets of inputs form synapses onto different regions of the same dendrite. Blocking NMDA receptors during later stages of circuit development did not disrupt segregation, indicating a critical period for activity-dependent shaping of patterns of innervation. DOI: http://dx.doi.org/10.7554/eLife.20502.001
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spelling pubmed-51353932016-12-05 An NMDA receptor-dependent mechanism for subcellular segregation of sensory inputs in the tadpole optic tectum Hamodi, Ali S Liu, Zhenyu Pratt, Kara G eLife Neuroscience In the vertebrate CNS, afferent sensory inputs are targeted to specific depths or layers of their target neuropil. This patterning exists ab initio, from the very beginning, and therefore has been considered an activity-independent process. However, here we report that, during circuit development, the subcellular segregation of the visual and mechanosensory inputs to specific regions of tectal neuron dendrites in the tadpole optic tectum requires NMDA receptor activity. Blocking NMDARs during the formation of these sensory circuits, or removing the visual set of inputs, leads to less defined segregation, and suggests a correlation-based mechanism in which correlated inputs wire to common regions of dendrites. This can account for how two sets of inputs form synapses onto different regions of the same dendrite. Blocking NMDA receptors during later stages of circuit development did not disrupt segregation, indicating a critical period for activity-dependent shaping of patterns of innervation. DOI: http://dx.doi.org/10.7554/eLife.20502.001 eLife Sciences Publications, Ltd 2016-11-23 /pmc/articles/PMC5135393/ /pubmed/27879199 http://dx.doi.org/10.7554/eLife.20502 Text en © 2016, Hamodi et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Hamodi, Ali S
Liu, Zhenyu
Pratt, Kara G
An NMDA receptor-dependent mechanism for subcellular segregation of sensory inputs in the tadpole optic tectum
title An NMDA receptor-dependent mechanism for subcellular segregation of sensory inputs in the tadpole optic tectum
title_full An NMDA receptor-dependent mechanism for subcellular segregation of sensory inputs in the tadpole optic tectum
title_fullStr An NMDA receptor-dependent mechanism for subcellular segregation of sensory inputs in the tadpole optic tectum
title_full_unstemmed An NMDA receptor-dependent mechanism for subcellular segregation of sensory inputs in the tadpole optic tectum
title_short An NMDA receptor-dependent mechanism for subcellular segregation of sensory inputs in the tadpole optic tectum
title_sort nmda receptor-dependent mechanism for subcellular segregation of sensory inputs in the tadpole optic tectum
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5135393/
https://www.ncbi.nlm.nih.gov/pubmed/27879199
http://dx.doi.org/10.7554/eLife.20502
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