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CA1 cell activity sequences emerge after reorganization of network correlation structure during associative learning

Animals can learn causal relationships between pairs of stimuli separated in time and this ability depends on the hippocampus. Such learning is believed to emerge from alterations in network connectivity, but large-scale connectivity is difficult to measure directly, especially during learning. Here...

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Detalles Bibliográficos
Autores principales: Modi, Mehrab N, Dhawale, Ashesh K, Bhalla, Upinder S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964823/
https://www.ncbi.nlm.nih.gov/pubmed/24668171
http://dx.doi.org/10.7554/eLife.01982
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author Modi, Mehrab N
Dhawale, Ashesh K
Bhalla, Upinder S
author_facet Modi, Mehrab N
Dhawale, Ashesh K
Bhalla, Upinder S
author_sort Modi, Mehrab N
collection PubMed
description Animals can learn causal relationships between pairs of stimuli separated in time and this ability depends on the hippocampus. Such learning is believed to emerge from alterations in network connectivity, but large-scale connectivity is difficult to measure directly, especially during learning. Here, we show that area CA1 cells converge to time-locked firing sequences that bridge the two stimuli paired during training, and this phenomenon is coupled to a reorganization of network correlations. Using two-photon calcium imaging of mouse hippocampal neurons we find that co-time-tuned neurons exhibit enhanced spontaneous activity correlations that increase just prior to learning. While time-tuned cells are not spatially organized, spontaneously correlated cells do fall into distinct spatial clusters that change as a result of learning. We propose that the spatial re-organization of correlation clusters reflects global network connectivity changes that are responsible for the emergence of the sequentially-timed activity of cell-groups underlying the learned behavior. DOI: http://dx.doi.org/10.7554/eLife.01982.001
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spelling pubmed-39648232014-03-27 CA1 cell activity sequences emerge after reorganization of network correlation structure during associative learning Modi, Mehrab N Dhawale, Ashesh K Bhalla, Upinder S eLife Neuroscience Animals can learn causal relationships between pairs of stimuli separated in time and this ability depends on the hippocampus. Such learning is believed to emerge from alterations in network connectivity, but large-scale connectivity is difficult to measure directly, especially during learning. Here, we show that area CA1 cells converge to time-locked firing sequences that bridge the two stimuli paired during training, and this phenomenon is coupled to a reorganization of network correlations. Using two-photon calcium imaging of mouse hippocampal neurons we find that co-time-tuned neurons exhibit enhanced spontaneous activity correlations that increase just prior to learning. While time-tuned cells are not spatially organized, spontaneously correlated cells do fall into distinct spatial clusters that change as a result of learning. We propose that the spatial re-organization of correlation clusters reflects global network connectivity changes that are responsible for the emergence of the sequentially-timed activity of cell-groups underlying the learned behavior. DOI: http://dx.doi.org/10.7554/eLife.01982.001 eLife Sciences Publications, Ltd 2014-03-25 /pmc/articles/PMC3964823/ /pubmed/24668171 http://dx.doi.org/10.7554/eLife.01982 Text en Copyright © 2014, Modi et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Modi, Mehrab N
Dhawale, Ashesh K
Bhalla, Upinder S
CA1 cell activity sequences emerge after reorganization of network correlation structure during associative learning
title CA1 cell activity sequences emerge after reorganization of network correlation structure during associative learning
title_full CA1 cell activity sequences emerge after reorganization of network correlation structure during associative learning
title_fullStr CA1 cell activity sequences emerge after reorganization of network correlation structure during associative learning
title_full_unstemmed CA1 cell activity sequences emerge after reorganization of network correlation structure during associative learning
title_short CA1 cell activity sequences emerge after reorganization of network correlation structure during associative learning
title_sort ca1 cell activity sequences emerge after reorganization of network correlation structure during associative learning
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964823/
https://www.ncbi.nlm.nih.gov/pubmed/24668171
http://dx.doi.org/10.7554/eLife.01982
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