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Function and energy consumption constrain neuronal biophysics in a canonical computation: Coincidence detection

Neural morphology and membrane properties vary greatly between cell types in the nervous system. The computations and local circuit connectivity that neurons support are thought to be the key factors constraining the cells’ biophysical properties. Nevertheless, additional constraints can be expected...

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Detalles Bibliográficos
Autores principales: Remme, Michiel W. H., Rinzel, John, Schreiber, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312336/
https://www.ncbi.nlm.nih.gov/pubmed/30521528
http://dx.doi.org/10.1371/journal.pcbi.1006612
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author Remme, Michiel W. H.
Rinzel, John
Schreiber, Susanne
author_facet Remme, Michiel W. H.
Rinzel, John
Schreiber, Susanne
author_sort Remme, Michiel W. H.
collection PubMed
description Neural morphology and membrane properties vary greatly between cell types in the nervous system. The computations and local circuit connectivity that neurons support are thought to be the key factors constraining the cells’ biophysical properties. Nevertheless, additional constraints can be expected to further shape neuronal design. Here, we focus on a particularly energy-intense system (as indicated by metabolic markers): principal neurons in the medial superior olive (MSO) nucleus of the auditory brainstem. Based on a modeling approach, we show that a trade-off between the level of performance of a functionally relevant computation and energy consumption predicts optimal ranges for cell morphology and membrane properties. The biophysical parameters appear most strongly constrained by functional needs, while energy use is minimized as long as function can be maintained. The key factors that determine model performance and energy consumption are 1) the saturation of the synaptic conductance input and 2) the temporal resolution of the postsynaptic signals as they reach the soma, which is largely determined by active membrane properties. MSO cells seem to operate close to pareto optimality, i.e., the trade-off boundary between performance and energy consumption that is formed by the set of optimal models. Good performance for drastically lower costs could in theory be achieved by small neurons without dendrites, as seen in the avian auditory system, pointing to additional constraints for mammalian MSO cells, including their circuit connectivity.
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spelling pubmed-63123362019-01-08 Function and energy consumption constrain neuronal biophysics in a canonical computation: Coincidence detection Remme, Michiel W. H. Rinzel, John Schreiber, Susanne PLoS Comput Biol Research Article Neural morphology and membrane properties vary greatly between cell types in the nervous system. The computations and local circuit connectivity that neurons support are thought to be the key factors constraining the cells’ biophysical properties. Nevertheless, additional constraints can be expected to further shape neuronal design. Here, we focus on a particularly energy-intense system (as indicated by metabolic markers): principal neurons in the medial superior olive (MSO) nucleus of the auditory brainstem. Based on a modeling approach, we show that a trade-off between the level of performance of a functionally relevant computation and energy consumption predicts optimal ranges for cell morphology and membrane properties. The biophysical parameters appear most strongly constrained by functional needs, while energy use is minimized as long as function can be maintained. The key factors that determine model performance and energy consumption are 1) the saturation of the synaptic conductance input and 2) the temporal resolution of the postsynaptic signals as they reach the soma, which is largely determined by active membrane properties. MSO cells seem to operate close to pareto optimality, i.e., the trade-off boundary between performance and energy consumption that is formed by the set of optimal models. Good performance for drastically lower costs could in theory be achieved by small neurons without dendrites, as seen in the avian auditory system, pointing to additional constraints for mammalian MSO cells, including their circuit connectivity. Public Library of Science 2018-12-06 /pmc/articles/PMC6312336/ /pubmed/30521528 http://dx.doi.org/10.1371/journal.pcbi.1006612 Text en © 2018 Remme 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
Remme, Michiel W. H.
Rinzel, John
Schreiber, Susanne
Function and energy consumption constrain neuronal biophysics in a canonical computation: Coincidence detection
title Function and energy consumption constrain neuronal biophysics in a canonical computation: Coincidence detection
title_full Function and energy consumption constrain neuronal biophysics in a canonical computation: Coincidence detection
title_fullStr Function and energy consumption constrain neuronal biophysics in a canonical computation: Coincidence detection
title_full_unstemmed Function and energy consumption constrain neuronal biophysics in a canonical computation: Coincidence detection
title_short Function and energy consumption constrain neuronal biophysics in a canonical computation: Coincidence detection
title_sort function and energy consumption constrain neuronal biophysics in a canonical computation: coincidence detection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312336/
https://www.ncbi.nlm.nih.gov/pubmed/30521528
http://dx.doi.org/10.1371/journal.pcbi.1006612
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