Cargando…

Predicting how and when hidden neurons skew measured synaptic interactions

A major obstacle to understanding neural coding and computation is the fact that experimental recordings typically sample only a small fraction of the neurons in a circuit. Measured neural properties are skewed by interactions between recorded neurons and the “hidden” portion of the network. To prop...

Descripción completa

Detalles Bibliográficos
Autores principales: Brinkman, Braden A. W., Rieke, Fred, Shea-Brown, Eric, Buice, Michael A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219819/
https://www.ncbi.nlm.nih.gov/pubmed/30346943
http://dx.doi.org/10.1371/journal.pcbi.1006490
_version_ 1783368726652911616
author Brinkman, Braden A. W.
Rieke, Fred
Shea-Brown, Eric
Buice, Michael A.
author_facet Brinkman, Braden A. W.
Rieke, Fred
Shea-Brown, Eric
Buice, Michael A.
author_sort Brinkman, Braden A. W.
collection PubMed
description A major obstacle to understanding neural coding and computation is the fact that experimental recordings typically sample only a small fraction of the neurons in a circuit. Measured neural properties are skewed by interactions between recorded neurons and the “hidden” portion of the network. To properly interpret neural data and determine how biological structure gives rise to neural circuit function, we thus need a better understanding of the relationships between measured effective neural properties and the true underlying physiological properties. Here, we focus on how the effective spatiotemporal dynamics of the synaptic interactions between neurons are reshaped by coupling to unobserved neurons. We find that the effective interactions from a pre-synaptic neuron r′ to a post-synaptic neuron r can be decomposed into a sum of the true interaction from r′ to r plus corrections from every directed path from r′ to r through unobserved neurons. Importantly, the resulting formula reveals when the hidden units have—or do not have—major effects on reshaping the interactions among observed neurons. As a particular example of interest, we derive a formula for the impact of hidden units in random networks with “strong” coupling—connection weights that scale with [Image: see text] , where N is the network size, precisely the scaling observed in recent experiments. With this quantitative relationship between measured and true interactions, we can study how network properties shape effective interactions, which properties are relevant for neural computations, and how to manipulate effective interactions.
format Online
Article
Text
id pubmed-6219819
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-62198192018-11-19 Predicting how and when hidden neurons skew measured synaptic interactions Brinkman, Braden A. W. Rieke, Fred Shea-Brown, Eric Buice, Michael A. PLoS Comput Biol Research Article A major obstacle to understanding neural coding and computation is the fact that experimental recordings typically sample only a small fraction of the neurons in a circuit. Measured neural properties are skewed by interactions between recorded neurons and the “hidden” portion of the network. To properly interpret neural data and determine how biological structure gives rise to neural circuit function, we thus need a better understanding of the relationships between measured effective neural properties and the true underlying physiological properties. Here, we focus on how the effective spatiotemporal dynamics of the synaptic interactions between neurons are reshaped by coupling to unobserved neurons. We find that the effective interactions from a pre-synaptic neuron r′ to a post-synaptic neuron r can be decomposed into a sum of the true interaction from r′ to r plus corrections from every directed path from r′ to r through unobserved neurons. Importantly, the resulting formula reveals when the hidden units have—or do not have—major effects on reshaping the interactions among observed neurons. As a particular example of interest, we derive a formula for the impact of hidden units in random networks with “strong” coupling—connection weights that scale with [Image: see text] , where N is the network size, precisely the scaling observed in recent experiments. With this quantitative relationship between measured and true interactions, we can study how network properties shape effective interactions, which properties are relevant for neural computations, and how to manipulate effective interactions. Public Library of Science 2018-10-22 /pmc/articles/PMC6219819/ /pubmed/30346943 http://dx.doi.org/10.1371/journal.pcbi.1006490 Text en © 2018 Brinkman et al 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
Brinkman, Braden A. W.
Rieke, Fred
Shea-Brown, Eric
Buice, Michael A.
Predicting how and when hidden neurons skew measured synaptic interactions
title Predicting how and when hidden neurons skew measured synaptic interactions
title_full Predicting how and when hidden neurons skew measured synaptic interactions
title_fullStr Predicting how and when hidden neurons skew measured synaptic interactions
title_full_unstemmed Predicting how and when hidden neurons skew measured synaptic interactions
title_short Predicting how and when hidden neurons skew measured synaptic interactions
title_sort predicting how and when hidden neurons skew measured synaptic interactions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219819/
https://www.ncbi.nlm.nih.gov/pubmed/30346943
http://dx.doi.org/10.1371/journal.pcbi.1006490
work_keys_str_mv AT brinkmanbradenaw predictinghowandwhenhiddenneuronsskewmeasuredsynapticinteractions
AT riekefred predictinghowandwhenhiddenneuronsskewmeasuredsynapticinteractions
AT sheabrowneric predictinghowandwhenhiddenneuronsskewmeasuredsynapticinteractions
AT buicemichaela predictinghowandwhenhiddenneuronsskewmeasuredsynapticinteractions