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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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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 |
format | Online Article Text |
id | pubmed-4728129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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