Cargando…
A Dynamic Connectome Supports the Emergence of Stable Computational Function of Neural Circuits through Reward-Based Learning
Synaptic connections between neurons in the brain are dynamic because of continuously ongoing spine dynamics, axonal sprouting, and other processes. In fact, it was recently shown that the spontaneous synapse-autonomous component of spine dynamics is at least as large as the component that depends o...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913731/ https://www.ncbi.nlm.nih.gov/pubmed/29696150 http://dx.doi.org/10.1523/ENEURO.0301-17.2018 |
_version_ | 1783316595653738496 |
---|---|
author | Kappel, David Legenstein, Robert Habenschuss, Stefan Hsieh, Michael Maass, Wolfgang |
author_facet | Kappel, David Legenstein, Robert Habenschuss, Stefan Hsieh, Michael Maass, Wolfgang |
author_sort | Kappel, David |
collection | PubMed |
description | Synaptic connections between neurons in the brain are dynamic because of continuously ongoing spine dynamics, axonal sprouting, and other processes. In fact, it was recently shown that the spontaneous synapse-autonomous component of spine dynamics is at least as large as the component that depends on the history of pre- and postsynaptic neural activity. These data are inconsistent with common models for network plasticity and raise the following questions: how can neural circuits maintain a stable computational function in spite of these continuously ongoing processes, and what could be functional uses of these ongoing processes? Here, we present a rigorous theoretical framework for these seemingly stochastic spine dynamics and rewiring processes in the context of reward-based learning tasks. We show that spontaneous synapse-autonomous processes, in combination with reward signals such as dopamine, can explain the capability of networks of neurons in the brain to configure themselves for specific computational tasks, and to compensate automatically for later changes in the network or task. Furthermore, we show theoretically and through computer simulations that stable computational performance is compatible with continuously ongoing synapse-autonomous changes. After reaching good computational performance it causes primarily a slow drift of network architecture and dynamics in task-irrelevant dimensions, as observed for neural activity in motor cortex and other areas. On the more abstract level of reinforcement learning the resulting model gives rise to an understanding of reward-driven network plasticity as continuous sampling of network configurations. |
format | Online Article Text |
id | pubmed-5913731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-59137312018-04-25 A Dynamic Connectome Supports the Emergence of Stable Computational Function of Neural Circuits through Reward-Based Learning Kappel, David Legenstein, Robert Habenschuss, Stefan Hsieh, Michael Maass, Wolfgang eNeuro Theory/New Concepts Synaptic connections between neurons in the brain are dynamic because of continuously ongoing spine dynamics, axonal sprouting, and other processes. In fact, it was recently shown that the spontaneous synapse-autonomous component of spine dynamics is at least as large as the component that depends on the history of pre- and postsynaptic neural activity. These data are inconsistent with common models for network plasticity and raise the following questions: how can neural circuits maintain a stable computational function in spite of these continuously ongoing processes, and what could be functional uses of these ongoing processes? Here, we present a rigorous theoretical framework for these seemingly stochastic spine dynamics and rewiring processes in the context of reward-based learning tasks. We show that spontaneous synapse-autonomous processes, in combination with reward signals such as dopamine, can explain the capability of networks of neurons in the brain to configure themselves for specific computational tasks, and to compensate automatically for later changes in the network or task. Furthermore, we show theoretically and through computer simulations that stable computational performance is compatible with continuously ongoing synapse-autonomous changes. After reaching good computational performance it causes primarily a slow drift of network architecture and dynamics in task-irrelevant dimensions, as observed for neural activity in motor cortex and other areas. On the more abstract level of reinforcement learning the resulting model gives rise to an understanding of reward-driven network plasticity as continuous sampling of network configurations. Society for Neuroscience 2018-04-24 /pmc/articles/PMC5913731/ /pubmed/29696150 http://dx.doi.org/10.1523/ENEURO.0301-17.2018 Text en Copyright © 2018 Kappel et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Theory/New Concepts Kappel, David Legenstein, Robert Habenschuss, Stefan Hsieh, Michael Maass, Wolfgang A Dynamic Connectome Supports the Emergence of Stable Computational Function of Neural Circuits through Reward-Based Learning |
title | A Dynamic Connectome Supports the Emergence of Stable Computational Function of Neural Circuits through Reward-Based Learning |
title_full | A Dynamic Connectome Supports the Emergence of Stable Computational Function of Neural Circuits through Reward-Based Learning |
title_fullStr | A Dynamic Connectome Supports the Emergence of Stable Computational Function of Neural Circuits through Reward-Based Learning |
title_full_unstemmed | A Dynamic Connectome Supports the Emergence of Stable Computational Function of Neural Circuits through Reward-Based Learning |
title_short | A Dynamic Connectome Supports the Emergence of Stable Computational Function of Neural Circuits through Reward-Based Learning |
title_sort | dynamic connectome supports the emergence of stable computational function of neural circuits through reward-based learning |
topic | Theory/New Concepts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913731/ https://www.ncbi.nlm.nih.gov/pubmed/29696150 http://dx.doi.org/10.1523/ENEURO.0301-17.2018 |
work_keys_str_mv | AT kappeldavid adynamicconnectomesupportstheemergenceofstablecomputationalfunctionofneuralcircuitsthroughrewardbasedlearning AT legensteinrobert adynamicconnectomesupportstheemergenceofstablecomputationalfunctionofneuralcircuitsthroughrewardbasedlearning AT habenschussstefan adynamicconnectomesupportstheemergenceofstablecomputationalfunctionofneuralcircuitsthroughrewardbasedlearning AT hsiehmichael adynamicconnectomesupportstheemergenceofstablecomputationalfunctionofneuralcircuitsthroughrewardbasedlearning AT maasswolfgang adynamicconnectomesupportstheemergenceofstablecomputationalfunctionofneuralcircuitsthroughrewardbasedlearning AT kappeldavid dynamicconnectomesupportstheemergenceofstablecomputationalfunctionofneuralcircuitsthroughrewardbasedlearning AT legensteinrobert dynamicconnectomesupportstheemergenceofstablecomputationalfunctionofneuralcircuitsthroughrewardbasedlearning AT habenschussstefan dynamicconnectomesupportstheemergenceofstablecomputationalfunctionofneuralcircuitsthroughrewardbasedlearning AT hsiehmichael dynamicconnectomesupportstheemergenceofstablecomputationalfunctionofneuralcircuitsthroughrewardbasedlearning AT maasswolfgang dynamicconnectomesupportstheemergenceofstablecomputationalfunctionofneuralcircuitsthroughrewardbasedlearning |