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Reconstruction of recurrent synaptic connectivity of thousands of neurons from simulated spiking activity

Dynamics and function of neuronal networks are determined by their synaptic connectivity. Current experimental methods to analyze synaptic network structure on the cellular level, however, cover only small fractions of functional neuronal circuits, typically without a simultaneous record of neuronal...

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Detalles Bibliográficos
Autores principales: Zaytsev, Yury V., Morrison, Abigail, Deger, Moritz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493949/
https://www.ncbi.nlm.nih.gov/pubmed/26041729
http://dx.doi.org/10.1007/s10827-015-0565-5
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author Zaytsev, Yury V.
Morrison, Abigail
Deger, Moritz
author_facet Zaytsev, Yury V.
Morrison, Abigail
Deger, Moritz
author_sort Zaytsev, Yury V.
collection PubMed
description Dynamics and function of neuronal networks are determined by their synaptic connectivity. Current experimental methods to analyze synaptic network structure on the cellular level, however, cover only small fractions of functional neuronal circuits, typically without a simultaneous record of neuronal spiking activity. Here we present a method for the reconstruction of large recurrent neuronal networks from thousands of parallel spike train recordings. We employ maximum likelihood estimation of a generalized linear model of the spiking activity in continuous time. For this model the point process likelihood is concave, such that a global optimum of the parameters can be obtained by gradient ascent. Previous methods, including those of the same class, did not allow recurrent networks of that order of magnitude to be reconstructed due to prohibitive computational cost and numerical instabilities. We describe a minimal model that is optimized for large networks and an efficient scheme for its parallelized numerical optimization on generic computing clusters. For a simulated balanced random network of 1000 neurons, synaptic connectivity is recovered with a misclassification error rate of less than 1 % under ideal conditions. We show that the error rate remains low in a series of example cases under progressively less ideal conditions. Finally, we successfully reconstruct the connectivity of a hidden synfire chain that is embedded in a random network, which requires clustering of the network connectivity to reveal the synfire groups. Our results demonstrate how synaptic connectivity could potentially be inferred from large-scale parallel spike train recordings.
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spelling pubmed-44939492015-07-08 Reconstruction of recurrent synaptic connectivity of thousands of neurons from simulated spiking activity Zaytsev, Yury V. Morrison, Abigail Deger, Moritz J Comput Neurosci Article Dynamics and function of neuronal networks are determined by their synaptic connectivity. Current experimental methods to analyze synaptic network structure on the cellular level, however, cover only small fractions of functional neuronal circuits, typically without a simultaneous record of neuronal spiking activity. Here we present a method for the reconstruction of large recurrent neuronal networks from thousands of parallel spike train recordings. We employ maximum likelihood estimation of a generalized linear model of the spiking activity in continuous time. For this model the point process likelihood is concave, such that a global optimum of the parameters can be obtained by gradient ascent. Previous methods, including those of the same class, did not allow recurrent networks of that order of magnitude to be reconstructed due to prohibitive computational cost and numerical instabilities. We describe a minimal model that is optimized for large networks and an efficient scheme for its parallelized numerical optimization on generic computing clusters. For a simulated balanced random network of 1000 neurons, synaptic connectivity is recovered with a misclassification error rate of less than 1 % under ideal conditions. We show that the error rate remains low in a series of example cases under progressively less ideal conditions. Finally, we successfully reconstruct the connectivity of a hidden synfire chain that is embedded in a random network, which requires clustering of the network connectivity to reveal the synfire groups. Our results demonstrate how synaptic connectivity could potentially be inferred from large-scale parallel spike train recordings. Springer US 2015-06-04 2015 /pmc/articles/PMC4493949/ /pubmed/26041729 http://dx.doi.org/10.1007/s10827-015-0565-5 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Zaytsev, Yury V.
Morrison, Abigail
Deger, Moritz
Reconstruction of recurrent synaptic connectivity of thousands of neurons from simulated spiking activity
title Reconstruction of recurrent synaptic connectivity of thousands of neurons from simulated spiking activity
title_full Reconstruction of recurrent synaptic connectivity of thousands of neurons from simulated spiking activity
title_fullStr Reconstruction of recurrent synaptic connectivity of thousands of neurons from simulated spiking activity
title_full_unstemmed Reconstruction of recurrent synaptic connectivity of thousands of neurons from simulated spiking activity
title_short Reconstruction of recurrent synaptic connectivity of thousands of neurons from simulated spiking activity
title_sort reconstruction of recurrent synaptic connectivity of thousands of neurons from simulated spiking activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493949/
https://www.ncbi.nlm.nih.gov/pubmed/26041729
http://dx.doi.org/10.1007/s10827-015-0565-5
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