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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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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 |
format | Online Article Text |
id | pubmed-5135393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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