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REMOD: A Tool for Analyzing and Remodeling the Dendritic Architecture of Neural Cells

Dendritic morphology is a key determinant of how individual neurons acquire a unique signal processing profile. The highly branched dendritic structure that originates from the cell body, explores the surrounding 3D space in a fractal-like manner, until it reaches a certain amount of complexity. Its...

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Autores principales: Bozelos, Panagiotis, Stefanou, Stefanos S., Bouloukakis, Georgios, Melachrinos, Constantinos, Poirazi, Panayiota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701929/
https://www.ncbi.nlm.nih.gov/pubmed/26778971
http://dx.doi.org/10.3389/fnana.2015.00156
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author Bozelos, Panagiotis
Stefanou, Stefanos S.
Bouloukakis, Georgios
Melachrinos, Constantinos
Poirazi, Panayiota
author_facet Bozelos, Panagiotis
Stefanou, Stefanos S.
Bouloukakis, Georgios
Melachrinos, Constantinos
Poirazi, Panayiota
author_sort Bozelos, Panagiotis
collection PubMed
description Dendritic morphology is a key determinant of how individual neurons acquire a unique signal processing profile. The highly branched dendritic structure that originates from the cell body, explores the surrounding 3D space in a fractal-like manner, until it reaches a certain amount of complexity. Its shape undergoes significant alterations under various physiological or neuropathological conditions. Yet, despite the profound effect that these alterations can have on neuronal function, the causal relationship between the two remains largely elusive. The lack of a systematic approach for remodeling neural cells and their dendritic trees is a key limitation that contributes to this problem. Such causal relationships can be inferred via the use of large-scale neuronal models whereby the anatomical plasticity of neurons is accounted for, in order to enhance their biological relevance and hence their predictive performance. To facilitate this effort, we developed a computational tool named REMOD that allows the structural remodeling of any type of virtual neuron. REMOD is written in Python and can be accessed through a dedicated web interface that guides the user through various options to manipulate selected neuronal morphologies. REMOD can also be used to extract meaningful morphology statistics for one or multiple reconstructions, including features such as sholl analysis, total dendritic length and area, path length to the soma, centrifugal branch order, diameter tapering and more. As such, the tool can be used both for the analysis and/or the remodeling of neuronal morphologies of any type.
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spelling pubmed-47019292016-01-15 REMOD: A Tool for Analyzing and Remodeling the Dendritic Architecture of Neural Cells Bozelos, Panagiotis Stefanou, Stefanos S. Bouloukakis, Georgios Melachrinos, Constantinos Poirazi, Panayiota Front Neuroanat Neuroscience Dendritic morphology is a key determinant of how individual neurons acquire a unique signal processing profile. The highly branched dendritic structure that originates from the cell body, explores the surrounding 3D space in a fractal-like manner, until it reaches a certain amount of complexity. Its shape undergoes significant alterations under various physiological or neuropathological conditions. Yet, despite the profound effect that these alterations can have on neuronal function, the causal relationship between the two remains largely elusive. The lack of a systematic approach for remodeling neural cells and their dendritic trees is a key limitation that contributes to this problem. Such causal relationships can be inferred via the use of large-scale neuronal models whereby the anatomical plasticity of neurons is accounted for, in order to enhance their biological relevance and hence their predictive performance. To facilitate this effort, we developed a computational tool named REMOD that allows the structural remodeling of any type of virtual neuron. REMOD is written in Python and can be accessed through a dedicated web interface that guides the user through various options to manipulate selected neuronal morphologies. REMOD can also be used to extract meaningful morphology statistics for one or multiple reconstructions, including features such as sholl analysis, total dendritic length and area, path length to the soma, centrifugal branch order, diameter tapering and more. As such, the tool can be used both for the analysis and/or the remodeling of neuronal morphologies of any type. Frontiers Media S.A. 2016-01-06 /pmc/articles/PMC4701929/ /pubmed/26778971 http://dx.doi.org/10.3389/fnana.2015.00156 Text en Copyright © 2016 Bozelos, Stefanou, Bouloukakis, Melachrinos and Poirazi. 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 and 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
Bozelos, Panagiotis
Stefanou, Stefanos S.
Bouloukakis, Georgios
Melachrinos, Constantinos
Poirazi, Panayiota
REMOD: A Tool for Analyzing and Remodeling the Dendritic Architecture of Neural Cells
title REMOD: A Tool for Analyzing and Remodeling the Dendritic Architecture of Neural Cells
title_full REMOD: A Tool for Analyzing and Remodeling the Dendritic Architecture of Neural Cells
title_fullStr REMOD: A Tool for Analyzing and Remodeling the Dendritic Architecture of Neural Cells
title_full_unstemmed REMOD: A Tool for Analyzing and Remodeling the Dendritic Architecture of Neural Cells
title_short REMOD: A Tool for Analyzing and Remodeling the Dendritic Architecture of Neural Cells
title_sort remod: a tool for analyzing and remodeling the dendritic architecture of neural cells
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701929/
https://www.ncbi.nlm.nih.gov/pubmed/26778971
http://dx.doi.org/10.3389/fnana.2015.00156
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