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Multivariate analysis of electrophysiological diversity of Xenopus visual neurons during development and plasticity

Biophysical properties of neurons become increasingly diverse over development, but mechanisms underlying and constraining this diversity are not fully understood. Here we investigate electrophysiological characteristics of Xenopus tadpole midbrain neurons across development and during homeostatic p...

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Autores principales: Ciarleglio, Christopher M, Khakhalin, Arseny S, Wang, Angelia F, Constantino, Alexander C, Yip, Sarah P, Aizenman, Carlos D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728129/
https://www.ncbi.nlm.nih.gov/pubmed/26568314
http://dx.doi.org/10.7554/eLife.11351
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author Ciarleglio, Christopher M
Khakhalin, Arseny S
Wang, Angelia F
Constantino, Alexander C
Yip, Sarah P
Aizenman, Carlos D
author_facet Ciarleglio, Christopher M
Khakhalin, Arseny S
Wang, Angelia F
Constantino, Alexander C
Yip, Sarah P
Aizenman, Carlos D
author_sort Ciarleglio, Christopher M
collection PubMed
description Biophysical properties of neurons become increasingly diverse over development, but mechanisms underlying and constraining this diversity are not fully understood. Here we investigate electrophysiological characteristics of Xenopus tadpole midbrain neurons across development and during homeostatic plasticity induced by patterned visual stimulation. We show that in development tectal neuron properties not only change on average, but also become increasingly diverse. After sensory stimulation, both electrophysiological diversity and functional differentiation of cells are reduced. At the same time, the amount of cross-correlations between cell properties increase after patterned stimulation as a result of homeostatic plasticity. We show that tectal neurons with similar spiking profiles often have strikingly different electrophysiological properties, and demonstrate that changes in intrinsic excitability during development and in response to sensory stimulation are mediated by different underlying mechanisms. Overall, this analysis and the accompanying dataset provide a unique framework for further studies of network maturation in Xenopus tadpoles. DOI: http://dx.doi.org/10.7554/eLife.11351.001
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spelling pubmed-47281292016-03-17 Multivariate analysis of electrophysiological diversity of Xenopus visual neurons during development and plasticity Ciarleglio, Christopher M Khakhalin, Arseny S Wang, Angelia F Constantino, Alexander C Yip, Sarah P Aizenman, Carlos D eLife Neuroscience Biophysical properties of neurons become increasingly diverse over development, but mechanisms underlying and constraining this diversity are not fully understood. Here we investigate electrophysiological characteristics of Xenopus tadpole midbrain neurons across development and during homeostatic plasticity induced by patterned visual stimulation. We show that in development tectal neuron properties not only change on average, but also become increasingly diverse. After sensory stimulation, both electrophysiological diversity and functional differentiation of cells are reduced. At the same time, the amount of cross-correlations between cell properties increase after patterned stimulation as a result of homeostatic plasticity. We show that tectal neurons with similar spiking profiles often have strikingly different electrophysiological properties, and demonstrate that changes in intrinsic excitability during development and in response to sensory stimulation are mediated by different underlying mechanisms. Overall, this analysis and the accompanying dataset provide a unique framework for further studies of network maturation in Xenopus tadpoles. DOI: http://dx.doi.org/10.7554/eLife.11351.001 eLife Sciences Publications, Ltd 2015-11-14 /pmc/articles/PMC4728129/ /pubmed/26568314 http://dx.doi.org/10.7554/eLife.11351 Text en © 2015, Ciarleglio 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
Ciarleglio, Christopher M
Khakhalin, Arseny S
Wang, Angelia F
Constantino, Alexander C
Yip, Sarah P
Aizenman, Carlos D
Multivariate analysis of electrophysiological diversity of Xenopus visual neurons during development and plasticity
title Multivariate analysis of electrophysiological diversity of Xenopus visual neurons during development and plasticity
title_full Multivariate analysis of electrophysiological diversity of Xenopus visual neurons during development and plasticity
title_fullStr Multivariate analysis of electrophysiological diversity of Xenopus visual neurons during development and plasticity
title_full_unstemmed Multivariate analysis of electrophysiological diversity of Xenopus visual neurons during development and plasticity
title_short Multivariate analysis of electrophysiological diversity of Xenopus visual neurons during development and plasticity
title_sort multivariate analysis of electrophysiological diversity of xenopus visual neurons during development and plasticity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728129/
https://www.ncbi.nlm.nih.gov/pubmed/26568314
http://dx.doi.org/10.7554/eLife.11351
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