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A General Procedure to Study Subcellular Models of Transsynaptic Signaling at Inhibitory Synapses

Computational modeling of brain circuits requires the definition of many parameters that are difficult to determine from experimental findings. One way to help interpret these data is to fit them using a particular kinetic model. In this paper, we propose a general procedure to fit individual synapt...

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Autores principales: Lupascu, Carmen A., Morabito, Annunziato, Merenda, Elisabetta, Marinelli, Silvia, Marchetti, Cristina, Migliore, Rosanna, Cherubini, Enrico, Migliore, Michele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928468/
https://www.ncbi.nlm.nih.gov/pubmed/27445784
http://dx.doi.org/10.3389/fninf.2016.00023
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author Lupascu, Carmen A.
Morabito, Annunziato
Merenda, Elisabetta
Marinelli, Silvia
Marchetti, Cristina
Migliore, Rosanna
Cherubini, Enrico
Migliore, Michele
author_facet Lupascu, Carmen A.
Morabito, Annunziato
Merenda, Elisabetta
Marinelli, Silvia
Marchetti, Cristina
Migliore, Rosanna
Cherubini, Enrico
Migliore, Michele
author_sort Lupascu, Carmen A.
collection PubMed
description Computational modeling of brain circuits requires the definition of many parameters that are difficult to determine from experimental findings. One way to help interpret these data is to fit them using a particular kinetic model. In this paper, we propose a general procedure to fit individual synaptic events recorded from voltage clamp experiments. Starting from any given model description (mod file) in the NEURON simulation environment, the procedure exploits user-defined constraints, dependencies, and rules for the parameters of the model to fit the time course of individual spontaneous synaptic events that are recorded experimentally. The procedure, implemented in NEURON, is currently available in ModelDB. A Python version is installed, and will be soon available for public use, as a standalone task in the Collaboratory Portal of the Human Brain Project. To illustrate the potential application of the procedure, we tested its use with various sets of experimental data on GABAergic synapses; gephyrin and gephyrin-dependent pathways were chosen as a suitable example of a kinetic model of synaptic transmission. For individual spontaneous inhibitory events in hippocampal pyramidal CA1 neurons, we found that gephyrin-dependent subcellular pathways may shape synaptic events at different levels, and can be correlated with cell- or event-specific activity history and/or pathological conditions.
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spelling pubmed-49284682016-07-21 A General Procedure to Study Subcellular Models of Transsynaptic Signaling at Inhibitory Synapses Lupascu, Carmen A. Morabito, Annunziato Merenda, Elisabetta Marinelli, Silvia Marchetti, Cristina Migliore, Rosanna Cherubini, Enrico Migliore, Michele Front Neuroinform Neuroscience Computational modeling of brain circuits requires the definition of many parameters that are difficult to determine from experimental findings. One way to help interpret these data is to fit them using a particular kinetic model. In this paper, we propose a general procedure to fit individual synaptic events recorded from voltage clamp experiments. Starting from any given model description (mod file) in the NEURON simulation environment, the procedure exploits user-defined constraints, dependencies, and rules for the parameters of the model to fit the time course of individual spontaneous synaptic events that are recorded experimentally. The procedure, implemented in NEURON, is currently available in ModelDB. A Python version is installed, and will be soon available for public use, as a standalone task in the Collaboratory Portal of the Human Brain Project. To illustrate the potential application of the procedure, we tested its use with various sets of experimental data on GABAergic synapses; gephyrin and gephyrin-dependent pathways were chosen as a suitable example of a kinetic model of synaptic transmission. For individual spontaneous inhibitory events in hippocampal pyramidal CA1 neurons, we found that gephyrin-dependent subcellular pathways may shape synaptic events at different levels, and can be correlated with cell- or event-specific activity history and/or pathological conditions. Frontiers Media S.A. 2016-06-30 /pmc/articles/PMC4928468/ /pubmed/27445784 http://dx.doi.org/10.3389/fninf.2016.00023 Text en Copyright © 2016 Lupascu, Morabito, Merenda, Marinelli, Marchetti, Migliore, Cherubini and Migliore. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Lupascu, Carmen A.
Morabito, Annunziato
Merenda, Elisabetta
Marinelli, Silvia
Marchetti, Cristina
Migliore, Rosanna
Cherubini, Enrico
Migliore, Michele
A General Procedure to Study Subcellular Models of Transsynaptic Signaling at Inhibitory Synapses
title A General Procedure to Study Subcellular Models of Transsynaptic Signaling at Inhibitory Synapses
title_full A General Procedure to Study Subcellular Models of Transsynaptic Signaling at Inhibitory Synapses
title_fullStr A General Procedure to Study Subcellular Models of Transsynaptic Signaling at Inhibitory Synapses
title_full_unstemmed A General Procedure to Study Subcellular Models of Transsynaptic Signaling at Inhibitory Synapses
title_short A General Procedure to Study Subcellular Models of Transsynaptic Signaling at Inhibitory Synapses
title_sort general procedure to study subcellular models of transsynaptic signaling at inhibitory synapses
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928468/
https://www.ncbi.nlm.nih.gov/pubmed/27445784
http://dx.doi.org/10.3389/fninf.2016.00023
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