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Espina: A Tool for the Automated Segmentation and Counting of Synapses in Large Stacks of Electron Microscopy Images

The synapses in the cerebral cortex can be classified into two main types, Gray's type I and type II, which correspond to asymmetric (mostly glutamatergic excitatory) and symmetric (inhibitory GABAergic) synapses, respectively. Hence, the quantification and identification of their different typ...

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Detalles Bibliográficos
Autores principales: Morales, Juan, Alonso-Nanclares, Lidia, Rodríguez, José-Rodrigo, DeFelipe, Javier, Rodríguez, Ángel, Merchán-Pérez, Ángel
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099746/
https://www.ncbi.nlm.nih.gov/pubmed/21633491
http://dx.doi.org/10.3389/fnana.2011.00018
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author Morales, Juan
Alonso-Nanclares, Lidia
Rodríguez, José-Rodrigo
DeFelipe, Javier
Rodríguez, Ángel
Merchán-Pérez, Ángel
author_facet Morales, Juan
Alonso-Nanclares, Lidia
Rodríguez, José-Rodrigo
DeFelipe, Javier
Rodríguez, Ángel
Merchán-Pérez, Ángel
author_sort Morales, Juan
collection PubMed
description The synapses in the cerebral cortex can be classified into two main types, Gray's type I and type II, which correspond to asymmetric (mostly glutamatergic excitatory) and symmetric (inhibitory GABAergic) synapses, respectively. Hence, the quantification and identification of their different types and the proportions in which they are found, is extraordinarily important in terms of brain function. The ideal approach to calculate the number of synapses per unit volume is to analyze 3D samples reconstructed from serial sections. However, obtaining serial sections by transmission electron microscopy is an extremely time consuming and technically demanding task. Using focused ion beam/scanning electron microscope microscopy, we recently showed that virtually all synapses can be accurately identified as asymmetric or symmetric synapses when they are visualized, reconstructed, and quantified from large 3D tissue samples obtained in an automated manner. Nevertheless, the analysis, segmentation, and quantification of synapses is still a labor intensive procedure. Thus, novel solutions are currently necessary to deal with the large volume of data that is being generated by automated 3D electron microscopy. Accordingly, we have developed ESPINA, a software tool that performs the automated segmentation and counting of synapses in a reconstructed 3D volume of the cerebral cortex, and that greatly facilitates and accelerates these processes.
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spelling pubmed-30997462011-06-01 Espina: A Tool for the Automated Segmentation and Counting of Synapses in Large Stacks of Electron Microscopy Images Morales, Juan Alonso-Nanclares, Lidia Rodríguez, José-Rodrigo DeFelipe, Javier Rodríguez, Ángel Merchán-Pérez, Ángel Front Neuroanat Neuroscience The synapses in the cerebral cortex can be classified into two main types, Gray's type I and type II, which correspond to asymmetric (mostly glutamatergic excitatory) and symmetric (inhibitory GABAergic) synapses, respectively. Hence, the quantification and identification of their different types and the proportions in which they are found, is extraordinarily important in terms of brain function. The ideal approach to calculate the number of synapses per unit volume is to analyze 3D samples reconstructed from serial sections. However, obtaining serial sections by transmission electron microscopy is an extremely time consuming and technically demanding task. Using focused ion beam/scanning electron microscope microscopy, we recently showed that virtually all synapses can be accurately identified as asymmetric or symmetric synapses when they are visualized, reconstructed, and quantified from large 3D tissue samples obtained in an automated manner. Nevertheless, the analysis, segmentation, and quantification of synapses is still a labor intensive procedure. Thus, novel solutions are currently necessary to deal with the large volume of data that is being generated by automated 3D electron microscopy. Accordingly, we have developed ESPINA, a software tool that performs the automated segmentation and counting of synapses in a reconstructed 3D volume of the cerebral cortex, and that greatly facilitates and accelerates these processes. Frontiers Research Foundation 2011-03-18 /pmc/articles/PMC3099746/ /pubmed/21633491 http://dx.doi.org/10.3389/fnana.2011.00018 Text en Copyright © 2011 Morales, Alonso-Nanclares, Rodríguez, DeFelipe, Rodríguez and Merchán-Pérez. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and Frontiers Media SA, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Morales, Juan
Alonso-Nanclares, Lidia
Rodríguez, José-Rodrigo
DeFelipe, Javier
Rodríguez, Ángel
Merchán-Pérez, Ángel
Espina: A Tool for the Automated Segmentation and Counting of Synapses in Large Stacks of Electron Microscopy Images
title Espina: A Tool for the Automated Segmentation and Counting of Synapses in Large Stacks of Electron Microscopy Images
title_full Espina: A Tool for the Automated Segmentation and Counting of Synapses in Large Stacks of Electron Microscopy Images
title_fullStr Espina: A Tool for the Automated Segmentation and Counting of Synapses in Large Stacks of Electron Microscopy Images
title_full_unstemmed Espina: A Tool for the Automated Segmentation and Counting of Synapses in Large Stacks of Electron Microscopy Images
title_short Espina: A Tool for the Automated Segmentation and Counting of Synapses in Large Stacks of Electron Microscopy Images
title_sort espina: a tool for the automated segmentation and counting of synapses in large stacks of electron microscopy images
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099746/
https://www.ncbi.nlm.nih.gov/pubmed/21633491
http://dx.doi.org/10.3389/fnana.2011.00018
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