Cargando…
Higher-Order Synaptic Interactions Coordinate Dynamics in Recurrent Networks
Linking synaptic connectivity to dynamics is key to understanding information processing in neocortex. Circuit dynamics emerge from complex interactions of interconnected neurons, necessitating that links between connectivity and dynamics be evaluated at the network level. Here we map propagating ac...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991791/ https://www.ncbi.nlm.nih.gov/pubmed/27542093 http://dx.doi.org/10.1371/journal.pcbi.1005078 |
_version_ | 1782448908277907456 |
---|---|
author | Chambers, Brendan MacLean, Jason N. |
author_facet | Chambers, Brendan MacLean, Jason N. |
author_sort | Chambers, Brendan |
collection | PubMed |
description | Linking synaptic connectivity to dynamics is key to understanding information processing in neocortex. Circuit dynamics emerge from complex interactions of interconnected neurons, necessitating that links between connectivity and dynamics be evaluated at the network level. Here we map propagating activity in large neuronal ensembles from mouse neocortex and compare it to a recurrent network model, where connectivity can be precisely measured and manipulated. We find that a dynamical feature dominates statistical descriptions of propagating activity for both neocortex and the model: convergent clusters comprised of fan-in triangle motifs, where two input neurons are themselves connected. Fan-in triangles coordinate the timing of presynaptic inputs during ongoing activity to effectively generate postsynaptic spiking. As a result, paradoxically, fan-in triangles dominate the statistics of spike propagation even in randomly connected recurrent networks. Interplay between higher-order synaptic connectivity and the integrative properties of neurons constrains the structure of network dynamics and shapes the routing of information in neocortex. |
format | Online Article Text |
id | pubmed-4991791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-49917912016-09-12 Higher-Order Synaptic Interactions Coordinate Dynamics in Recurrent Networks Chambers, Brendan MacLean, Jason N. PLoS Comput Biol Research Article Linking synaptic connectivity to dynamics is key to understanding information processing in neocortex. Circuit dynamics emerge from complex interactions of interconnected neurons, necessitating that links between connectivity and dynamics be evaluated at the network level. Here we map propagating activity in large neuronal ensembles from mouse neocortex and compare it to a recurrent network model, where connectivity can be precisely measured and manipulated. We find that a dynamical feature dominates statistical descriptions of propagating activity for both neocortex and the model: convergent clusters comprised of fan-in triangle motifs, where two input neurons are themselves connected. Fan-in triangles coordinate the timing of presynaptic inputs during ongoing activity to effectively generate postsynaptic spiking. As a result, paradoxically, fan-in triangles dominate the statistics of spike propagation even in randomly connected recurrent networks. Interplay between higher-order synaptic connectivity and the integrative properties of neurons constrains the structure of network dynamics and shapes the routing of information in neocortex. Public Library of Science 2016-08-19 /pmc/articles/PMC4991791/ /pubmed/27542093 http://dx.doi.org/10.1371/journal.pcbi.1005078 Text en © 2016 Chambers, MacLean http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chambers, Brendan MacLean, Jason N. Higher-Order Synaptic Interactions Coordinate Dynamics in Recurrent Networks |
title | Higher-Order Synaptic Interactions Coordinate Dynamics in Recurrent Networks |
title_full | Higher-Order Synaptic Interactions Coordinate Dynamics in Recurrent Networks |
title_fullStr | Higher-Order Synaptic Interactions Coordinate Dynamics in Recurrent Networks |
title_full_unstemmed | Higher-Order Synaptic Interactions Coordinate Dynamics in Recurrent Networks |
title_short | Higher-Order Synaptic Interactions Coordinate Dynamics in Recurrent Networks |
title_sort | higher-order synaptic interactions coordinate dynamics in recurrent networks |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991791/ https://www.ncbi.nlm.nih.gov/pubmed/27542093 http://dx.doi.org/10.1371/journal.pcbi.1005078 |
work_keys_str_mv | AT chambersbrendan higherordersynapticinteractionscoordinatedynamicsinrecurrentnetworks AT macleanjasonn higherordersynapticinteractionscoordinatedynamicsinrecurrentnetworks |