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A cellular mechanism for inverse effectiveness in multisensory integration
To build a coherent view of the external world, an organism needs to integrate multiple types of sensory information from different sources, a process known as multisensory integration (MSI). Previously, we showed that the temporal dependence of MSI in the optic tectum of Xenopus laevis tadpoles is...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5375642/ https://www.ncbi.nlm.nih.gov/pubmed/28315524 http://dx.doi.org/10.7554/eLife.25392 |
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author | Truszkowski, Torrey LS Carrillo, Oscar A Bleier, Julia Ramirez-Vizcarrondo, Carolina M Felch, Daniel L McQuillan, Molly Truszkowski, Christopher P Khakhalin, Arseny S Aizenman, Carlos D |
author_facet | Truszkowski, Torrey LS Carrillo, Oscar A Bleier, Julia Ramirez-Vizcarrondo, Carolina M Felch, Daniel L McQuillan, Molly Truszkowski, Christopher P Khakhalin, Arseny S Aizenman, Carlos D |
author_sort | Truszkowski, Torrey LS |
collection | PubMed |
description | To build a coherent view of the external world, an organism needs to integrate multiple types of sensory information from different sources, a process known as multisensory integration (MSI). Previously, we showed that the temporal dependence of MSI in the optic tectum of Xenopus laevis tadpoles is mediated by the network dynamics of the recruitment of local inhibition by sensory input (Felch et al., 2016). This was one of the first cellular-level mechanisms described for MSI. Here, we expand this cellular level view of MSI by focusing on the principle of inverse effectiveness, another central feature of MSI stating that the amount of multisensory enhancement observed inversely depends on the size of unisensory responses. We show that non-linear summation of crossmodal synaptic responses, mediated by NMDA-type glutamate receptor (NMDARs) activation, form the cellular basis for inverse effectiveness, both at the cellular and behavioral levels. DOI: http://dx.doi.org/10.7554/eLife.25392.001 |
format | Online Article Text |
id | pubmed-5375642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53756422017-04-05 A cellular mechanism for inverse effectiveness in multisensory integration Truszkowski, Torrey LS Carrillo, Oscar A Bleier, Julia Ramirez-Vizcarrondo, Carolina M Felch, Daniel L McQuillan, Molly Truszkowski, Christopher P Khakhalin, Arseny S Aizenman, Carlos D eLife Neuroscience To build a coherent view of the external world, an organism needs to integrate multiple types of sensory information from different sources, a process known as multisensory integration (MSI). Previously, we showed that the temporal dependence of MSI in the optic tectum of Xenopus laevis tadpoles is mediated by the network dynamics of the recruitment of local inhibition by sensory input (Felch et al., 2016). This was one of the first cellular-level mechanisms described for MSI. Here, we expand this cellular level view of MSI by focusing on the principle of inverse effectiveness, another central feature of MSI stating that the amount of multisensory enhancement observed inversely depends on the size of unisensory responses. We show that non-linear summation of crossmodal synaptic responses, mediated by NMDA-type glutamate receptor (NMDARs) activation, form the cellular basis for inverse effectiveness, both at the cellular and behavioral levels. DOI: http://dx.doi.org/10.7554/eLife.25392.001 eLife Sciences Publications, Ltd 2017-03-18 /pmc/articles/PMC5375642/ /pubmed/28315524 http://dx.doi.org/10.7554/eLife.25392 Text en © 2017, Truszkowski 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 Truszkowski, Torrey LS Carrillo, Oscar A Bleier, Julia Ramirez-Vizcarrondo, Carolina M Felch, Daniel L McQuillan, Molly Truszkowski, Christopher P Khakhalin, Arseny S Aizenman, Carlos D A cellular mechanism for inverse effectiveness in multisensory integration |
title | A cellular mechanism for inverse effectiveness in multisensory integration |
title_full | A cellular mechanism for inverse effectiveness in multisensory integration |
title_fullStr | A cellular mechanism for inverse effectiveness in multisensory integration |
title_full_unstemmed | A cellular mechanism for inverse effectiveness in multisensory integration |
title_short | A cellular mechanism for inverse effectiveness in multisensory integration |
title_sort | cellular mechanism for inverse effectiveness in multisensory integration |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5375642/ https://www.ncbi.nlm.nih.gov/pubmed/28315524 http://dx.doi.org/10.7554/eLife.25392 |
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