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Reconstruction of genetically identified neurons imaged by serial-section electron microscopy
Resolving patterns of synaptic connectivity in neural circuits currently requires serial section electron microscopy. However, complete circuit reconstruction is prohibitively slow and may not be necessary for many purposes such as comparing neuronal structure and connectivity among multiple animals...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959841/ https://www.ncbi.nlm.nih.gov/pubmed/27383271 http://dx.doi.org/10.7554/eLife.15015 |
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author | Joesch, Maximilian Mankus, David Yamagata, Masahito Shahbazi, Ali Schalek, Richard Suissa-Peleg, Adi Meister, Markus Lichtman, Jeff W Scheirer, Walter J Sanes, Joshua R |
author_facet | Joesch, Maximilian Mankus, David Yamagata, Masahito Shahbazi, Ali Schalek, Richard Suissa-Peleg, Adi Meister, Markus Lichtman, Jeff W Scheirer, Walter J Sanes, Joshua R |
author_sort | Joesch, Maximilian |
collection | PubMed |
description | Resolving patterns of synaptic connectivity in neural circuits currently requires serial section electron microscopy. However, complete circuit reconstruction is prohibitively slow and may not be necessary for many purposes such as comparing neuronal structure and connectivity among multiple animals. Here, we present an alternative strategy, targeted reconstruction of specific neuronal types. We used viral vectors to deliver peroxidase derivatives, which catalyze production of an electron-dense tracer, to genetically identify neurons, and developed a protocol that enhances the electron-density of the labeled cells while retaining the quality of the ultrastructure. The high contrast of the marked neurons enabled two innovations that speed data acquisition: targeted high-resolution reimaging of regions selected from rapidly-acquired lower resolution reconstruction, and an unsupervised segmentation algorithm. This pipeline reduces imaging and reconstruction times by two orders of magnitude, facilitating directed inquiry of circuit motifs. DOI: http://dx.doi.org/10.7554/eLife.15015.001 |
format | Online Article Text |
id | pubmed-4959841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49598412016-07-28 Reconstruction of genetically identified neurons imaged by serial-section electron microscopy Joesch, Maximilian Mankus, David Yamagata, Masahito Shahbazi, Ali Schalek, Richard Suissa-Peleg, Adi Meister, Markus Lichtman, Jeff W Scheirer, Walter J Sanes, Joshua R eLife Cell Biology Resolving patterns of synaptic connectivity in neural circuits currently requires serial section electron microscopy. However, complete circuit reconstruction is prohibitively slow and may not be necessary for many purposes such as comparing neuronal structure and connectivity among multiple animals. Here, we present an alternative strategy, targeted reconstruction of specific neuronal types. We used viral vectors to deliver peroxidase derivatives, which catalyze production of an electron-dense tracer, to genetically identify neurons, and developed a protocol that enhances the electron-density of the labeled cells while retaining the quality of the ultrastructure. The high contrast of the marked neurons enabled two innovations that speed data acquisition: targeted high-resolution reimaging of regions selected from rapidly-acquired lower resolution reconstruction, and an unsupervised segmentation algorithm. This pipeline reduces imaging and reconstruction times by two orders of magnitude, facilitating directed inquiry of circuit motifs. DOI: http://dx.doi.org/10.7554/eLife.15015.001 eLife Sciences Publications, Ltd 2016-07-07 /pmc/articles/PMC4959841/ /pubmed/27383271 http://dx.doi.org/10.7554/eLife.15015 Text en © 2016, Joesch et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Joesch, Maximilian Mankus, David Yamagata, Masahito Shahbazi, Ali Schalek, Richard Suissa-Peleg, Adi Meister, Markus Lichtman, Jeff W Scheirer, Walter J Sanes, Joshua R Reconstruction of genetically identified neurons imaged by serial-section electron microscopy |
title | Reconstruction of genetically identified neurons imaged by serial-section electron microscopy |
title_full | Reconstruction of genetically identified neurons imaged by serial-section electron microscopy |
title_fullStr | Reconstruction of genetically identified neurons imaged by serial-section electron microscopy |
title_full_unstemmed | Reconstruction of genetically identified neurons imaged by serial-section electron microscopy |
title_short | Reconstruction of genetically identified neurons imaged by serial-section electron microscopy |
title_sort | reconstruction of genetically identified neurons imaged by serial-section electron microscopy |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959841/ https://www.ncbi.nlm.nih.gov/pubmed/27383271 http://dx.doi.org/10.7554/eLife.15015 |
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