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When do microcircuits produce beyond-pairwise correlations?
Describing the collective activity of neural populations is a daunting task. Recent empirical studies in retina, however, suggest a vast simplification in how multi-neuron spiking occurs: the activity patterns of retinal ganglion cell (RGC) populations under some conditions are nearly completely cap...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915758/ https://www.ncbi.nlm.nih.gov/pubmed/24567715 http://dx.doi.org/10.3389/fncom.2014.00010 |
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author | Barreiro, Andrea K. Gjorgjieva, Julijana Rieke, Fred Shea-Brown, Eric |
author_facet | Barreiro, Andrea K. Gjorgjieva, Julijana Rieke, Fred Shea-Brown, Eric |
author_sort | Barreiro, Andrea K. |
collection | PubMed |
description | Describing the collective activity of neural populations is a daunting task. Recent empirical studies in retina, however, suggest a vast simplification in how multi-neuron spiking occurs: the activity patterns of retinal ganglion cell (RGC) populations under some conditions are nearly completely captured by pairwise interactions among neurons. In other circumstances, higher-order statistics are required and appear to be shaped by input statistics and intrinsic circuit mechanisms. Here, we study the emergence of higher-order interactions in a model of the RGC circuit in which correlations are generated by common input. We quantify the impact of higher-order interactions by comparing the responses of mechanistic circuit models vs. “null” descriptions in which all higher-than-pairwise correlations have been accounted for by lower order statistics; these are known as pairwise maximum entropy (PME) models. We find that over a broad range of stimuli, output spiking patterns are surprisingly well captured by the pairwise model. To understand this finding, we study an analytically tractable simplification of the RGC model. We find that in the simplified model, bimodal input signals produce larger deviations from pairwise predictions than unimodal inputs. The characteristic light filtering properties of the upstream RGC circuitry suppress bimodality in light stimuli, thus removing a powerful source of higher-order interactions. This provides a novel explanation for the surprising empirical success of pairwise models. |
format | Online Article Text |
id | pubmed-3915758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39157582014-02-24 When do microcircuits produce beyond-pairwise correlations? Barreiro, Andrea K. Gjorgjieva, Julijana Rieke, Fred Shea-Brown, Eric Front Comput Neurosci Neuroscience Describing the collective activity of neural populations is a daunting task. Recent empirical studies in retina, however, suggest a vast simplification in how multi-neuron spiking occurs: the activity patterns of retinal ganglion cell (RGC) populations under some conditions are nearly completely captured by pairwise interactions among neurons. In other circumstances, higher-order statistics are required and appear to be shaped by input statistics and intrinsic circuit mechanisms. Here, we study the emergence of higher-order interactions in a model of the RGC circuit in which correlations are generated by common input. We quantify the impact of higher-order interactions by comparing the responses of mechanistic circuit models vs. “null” descriptions in which all higher-than-pairwise correlations have been accounted for by lower order statistics; these are known as pairwise maximum entropy (PME) models. We find that over a broad range of stimuli, output spiking patterns are surprisingly well captured by the pairwise model. To understand this finding, we study an analytically tractable simplification of the RGC model. We find that in the simplified model, bimodal input signals produce larger deviations from pairwise predictions than unimodal inputs. The characteristic light filtering properties of the upstream RGC circuitry suppress bimodality in light stimuli, thus removing a powerful source of higher-order interactions. This provides a novel explanation for the surprising empirical success of pairwise models. Frontiers Media S.A. 2014-02-06 /pmc/articles/PMC3915758/ /pubmed/24567715 http://dx.doi.org/10.3389/fncom.2014.00010 Text en Copyright © 2014 Barreiro, Gjorgjieva, Rieke and Shea-Brown. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Barreiro, Andrea K. Gjorgjieva, Julijana Rieke, Fred Shea-Brown, Eric When do microcircuits produce beyond-pairwise correlations? |
title | When do microcircuits produce beyond-pairwise correlations? |
title_full | When do microcircuits produce beyond-pairwise correlations? |
title_fullStr | When do microcircuits produce beyond-pairwise correlations? |
title_full_unstemmed | When do microcircuits produce beyond-pairwise correlations? |
title_short | When do microcircuits produce beyond-pairwise correlations? |
title_sort | when do microcircuits produce beyond-pairwise correlations? |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915758/ https://www.ncbi.nlm.nih.gov/pubmed/24567715 http://dx.doi.org/10.3389/fncom.2014.00010 |
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