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Postsynaptic Signal Transduction Models for Long-Term Potentiation and Depression

More than a hundred biochemical species, activated by neurotransmitters binding to transmembrane receptors, are important in long-term potentiation (LTP) and long-term depression (LTD). To investigate which species and interactions are critical for synaptic plasticity, many computational postsynapti...

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Autores principales: Manninen, Tiina, Hituri, Katri, Kotaleski, Jeanette Hellgren, Blackwell, Kim T., Linne, Marja-Leena
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006457/
https://www.ncbi.nlm.nih.gov/pubmed/21188161
http://dx.doi.org/10.3389/fncom.2010.00152
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author Manninen, Tiina
Hituri, Katri
Kotaleski, Jeanette Hellgren
Blackwell, Kim T.
Linne, Marja-Leena
author_facet Manninen, Tiina
Hituri, Katri
Kotaleski, Jeanette Hellgren
Blackwell, Kim T.
Linne, Marja-Leena
author_sort Manninen, Tiina
collection PubMed
description More than a hundred biochemical species, activated by neurotransmitters binding to transmembrane receptors, are important in long-term potentiation (LTP) and long-term depression (LTD). To investigate which species and interactions are critical for synaptic plasticity, many computational postsynaptic signal transduction models have been developed. The models range from simple models with a single reversible reaction to detailed models with several hundred kinetic reactions. In this study, more than a hundred models are reviewed, and their features are compared and contrasted so that similarities and differences are more readily apparent. The models are classified according to the type of synaptic plasticity that is modeled (LTP or LTD) and whether they include diffusion or electrophysiological phenomena. Other characteristics that discriminate the models include the phase of synaptic plasticity modeled (induction, expression, or maintenance) and the simulation method used (deterministic or stochastic). We find that models are becoming increasingly sophisticated, by including stochastic properties, integrating with electrophysiological properties of entire neurons, or incorporating diffusion of signaling molecules. Simpler models continue to be developed because they are computationally efficient and allow theoretical analysis. The more complex models permit investigation of mechanisms underlying specific properties and experimental verification of model predictions. Nonetheless, it is difficult to fully comprehend the evolution of these models because (1) several models are not described in detail in the publications, (2) only a few models are provided in existing model databases, and (3) comparison to previous models is lacking. We conclude that the value of these models for understanding molecular mechanisms of synaptic plasticity is increasing and will be enhanced further with more complete descriptions and sharing of the published models.
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spelling pubmed-30064572010-12-23 Postsynaptic Signal Transduction Models for Long-Term Potentiation and Depression Manninen, Tiina Hituri, Katri Kotaleski, Jeanette Hellgren Blackwell, Kim T. Linne, Marja-Leena Front Comput Neurosci Neuroscience More than a hundred biochemical species, activated by neurotransmitters binding to transmembrane receptors, are important in long-term potentiation (LTP) and long-term depression (LTD). To investigate which species and interactions are critical for synaptic plasticity, many computational postsynaptic signal transduction models have been developed. The models range from simple models with a single reversible reaction to detailed models with several hundred kinetic reactions. In this study, more than a hundred models are reviewed, and their features are compared and contrasted so that similarities and differences are more readily apparent. The models are classified according to the type of synaptic plasticity that is modeled (LTP or LTD) and whether they include diffusion or electrophysiological phenomena. Other characteristics that discriminate the models include the phase of synaptic plasticity modeled (induction, expression, or maintenance) and the simulation method used (deterministic or stochastic). We find that models are becoming increasingly sophisticated, by including stochastic properties, integrating with electrophysiological properties of entire neurons, or incorporating diffusion of signaling molecules. Simpler models continue to be developed because they are computationally efficient and allow theoretical analysis. The more complex models permit investigation of mechanisms underlying specific properties and experimental verification of model predictions. Nonetheless, it is difficult to fully comprehend the evolution of these models because (1) several models are not described in detail in the publications, (2) only a few models are provided in existing model databases, and (3) comparison to previous models is lacking. We conclude that the value of these models for understanding molecular mechanisms of synaptic plasticity is increasing and will be enhanced further with more complete descriptions and sharing of the published models. Frontiers Research Foundation 2010-12-13 /pmc/articles/PMC3006457/ /pubmed/21188161 http://dx.doi.org/10.3389/fncom.2010.00152 Text en Copyright © 2010 Manninen, Hituri, Hellgren Kotaleski, Blackwell and Linne. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Manninen, Tiina
Hituri, Katri
Kotaleski, Jeanette Hellgren
Blackwell, Kim T.
Linne, Marja-Leena
Postsynaptic Signal Transduction Models for Long-Term Potentiation and Depression
title Postsynaptic Signal Transduction Models for Long-Term Potentiation and Depression
title_full Postsynaptic Signal Transduction Models for Long-Term Potentiation and Depression
title_fullStr Postsynaptic Signal Transduction Models for Long-Term Potentiation and Depression
title_full_unstemmed Postsynaptic Signal Transduction Models for Long-Term Potentiation and Depression
title_short Postsynaptic Signal Transduction Models for Long-Term Potentiation and Depression
title_sort postsynaptic signal transduction models for long-term potentiation and depression
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006457/
https://www.ncbi.nlm.nih.gov/pubmed/21188161
http://dx.doi.org/10.3389/fncom.2010.00152
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