Cargando…
Cortical reliability amid noise and chaos
Typical responses of cortical neurons to identical sensory stimuli appear highly variable. It has thus been proposed that the cortex primarily uses a rate code. However, other studies have argued for spike-time coding under certain conditions. The potential role of spike-time coding is directly limi...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706377/ https://www.ncbi.nlm.nih.gov/pubmed/31439838 http://dx.doi.org/10.1038/s41467-019-11633-8 |
_version_ | 1783445688060739584 |
---|---|
author | Nolte, Max Reimann, Michael W. King, James G. Markram, Henry Muller, Eilif B. |
author_facet | Nolte, Max Reimann, Michael W. King, James G. Markram, Henry Muller, Eilif B. |
author_sort | Nolte, Max |
collection | PubMed |
description | Typical responses of cortical neurons to identical sensory stimuli appear highly variable. It has thus been proposed that the cortex primarily uses a rate code. However, other studies have argued for spike-time coding under certain conditions. The potential role of spike-time coding is directly limited by the internally generated variability of cortical circuits, which remains largely unexplored. Here, we quantify this internally generated variability using a biophysical model of rat neocortical microcircuitry with biologically realistic noise sources. We find that stochastic neurotransmitter release is a critical component of internally generated variability, causing rapidly diverging, chaotic recurrent network dynamics. Surprisingly, the same nonlinear recurrent network dynamics can transiently overcome the chaos in response to weak feed-forward thalamocortical inputs, and support reliable spike times with millisecond precision. Our model shows that the noisy and chaotic network dynamics of recurrent cortical microcircuitry are compatible with stimulus-evoked, millisecond spike-time reliability, resolving a long-standing debate. |
format | Online Article Text |
id | pubmed-6706377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67063772019-08-26 Cortical reliability amid noise and chaos Nolte, Max Reimann, Michael W. King, James G. Markram, Henry Muller, Eilif B. Nat Commun Article Typical responses of cortical neurons to identical sensory stimuli appear highly variable. It has thus been proposed that the cortex primarily uses a rate code. However, other studies have argued for spike-time coding under certain conditions. The potential role of spike-time coding is directly limited by the internally generated variability of cortical circuits, which remains largely unexplored. Here, we quantify this internally generated variability using a biophysical model of rat neocortical microcircuitry with biologically realistic noise sources. We find that stochastic neurotransmitter release is a critical component of internally generated variability, causing rapidly diverging, chaotic recurrent network dynamics. Surprisingly, the same nonlinear recurrent network dynamics can transiently overcome the chaos in response to weak feed-forward thalamocortical inputs, and support reliable spike times with millisecond precision. Our model shows that the noisy and chaotic network dynamics of recurrent cortical microcircuitry are compatible with stimulus-evoked, millisecond spike-time reliability, resolving a long-standing debate. Nature Publishing Group UK 2019-08-22 /pmc/articles/PMC6706377/ /pubmed/31439838 http://dx.doi.org/10.1038/s41467-019-11633-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Nolte, Max Reimann, Michael W. King, James G. Markram, Henry Muller, Eilif B. Cortical reliability amid noise and chaos |
title | Cortical reliability amid noise and chaos |
title_full | Cortical reliability amid noise and chaos |
title_fullStr | Cortical reliability amid noise and chaos |
title_full_unstemmed | Cortical reliability amid noise and chaos |
title_short | Cortical reliability amid noise and chaos |
title_sort | cortical reliability amid noise and chaos |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706377/ https://www.ncbi.nlm.nih.gov/pubmed/31439838 http://dx.doi.org/10.1038/s41467-019-11633-8 |
work_keys_str_mv | AT noltemax corticalreliabilityamidnoiseandchaos AT reimannmichaelw corticalreliabilityamidnoiseandchaos AT kingjamesg corticalreliabilityamidnoiseandchaos AT markramhenry corticalreliabilityamidnoiseandchaos AT mullereilifb corticalreliabilityamidnoiseandchaos |