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An optogenetic toolbox for unbiased discovery of functionally connected cells in neural circuits
Optical imaging approaches have revolutionized our ability to monitor neural network dynamics, but by themselves are unable to link a neuron’s activity to its functional connectivity. We present a versatile genetic toolbox, termed ‘Optobow’, for all-optical discovery of excitatory connections in viv...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524645/ https://www.ncbi.nlm.nih.gov/pubmed/28740141 http://dx.doi.org/10.1038/s41467-017-00160-z |
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author | Förster, Dominique Dal Maschio, Marco Laurell, Eva Baier, Herwig |
author_facet | Förster, Dominique Dal Maschio, Marco Laurell, Eva Baier, Herwig |
author_sort | Förster, Dominique |
collection | PubMed |
description | Optical imaging approaches have revolutionized our ability to monitor neural network dynamics, but by themselves are unable to link a neuron’s activity to its functional connectivity. We present a versatile genetic toolbox, termed ‘Optobow’, for all-optical discovery of excitatory connections in vivo. By combining the Gal4-UAS system with Cre/lox recombination, we target the optogenetic actuator ChrimsonR and the sensor GCaMP6 to stochastically labeled, nonoverlapping and sparse subsets of neurons. Photostimulation of single cells using two-photon computer-generated holography evokes calcium responses in downstream neurons. Morphological reconstruction of neurite arbors, response latencies and localization of presynaptic markers suggest that some neuron pairs recorded here are directly connected, while others are two or more synapses apart from each other. With this toolbox, we discover wiring principles between specific cell types in the larval zebrafish tectum. Optobow should be useful for identification and manipulation of networks of interconnected neurons, even in dense neural tissues. |
format | Online Article Text |
id | pubmed-5524645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55246452017-07-28 An optogenetic toolbox for unbiased discovery of functionally connected cells in neural circuits Förster, Dominique Dal Maschio, Marco Laurell, Eva Baier, Herwig Nat Commun Article Optical imaging approaches have revolutionized our ability to monitor neural network dynamics, but by themselves are unable to link a neuron’s activity to its functional connectivity. We present a versatile genetic toolbox, termed ‘Optobow’, for all-optical discovery of excitatory connections in vivo. By combining the Gal4-UAS system with Cre/lox recombination, we target the optogenetic actuator ChrimsonR and the sensor GCaMP6 to stochastically labeled, nonoverlapping and sparse subsets of neurons. Photostimulation of single cells using two-photon computer-generated holography evokes calcium responses in downstream neurons. Morphological reconstruction of neurite arbors, response latencies and localization of presynaptic markers suggest that some neuron pairs recorded here are directly connected, while others are two or more synapses apart from each other. With this toolbox, we discover wiring principles between specific cell types in the larval zebrafish tectum. Optobow should be useful for identification and manipulation of networks of interconnected neurons, even in dense neural tissues. Nature Publishing Group UK 2017-07-24 /pmc/articles/PMC5524645/ /pubmed/28740141 http://dx.doi.org/10.1038/s41467-017-00160-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Förster, Dominique Dal Maschio, Marco Laurell, Eva Baier, Herwig An optogenetic toolbox for unbiased discovery of functionally connected cells in neural circuits |
title | An optogenetic toolbox for unbiased discovery of functionally connected cells in neural circuits |
title_full | An optogenetic toolbox for unbiased discovery of functionally connected cells in neural circuits |
title_fullStr | An optogenetic toolbox for unbiased discovery of functionally connected cells in neural circuits |
title_full_unstemmed | An optogenetic toolbox for unbiased discovery of functionally connected cells in neural circuits |
title_short | An optogenetic toolbox for unbiased discovery of functionally connected cells in neural circuits |
title_sort | optogenetic toolbox for unbiased discovery of functionally connected cells in neural circuits |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524645/ https://www.ncbi.nlm.nih.gov/pubmed/28740141 http://dx.doi.org/10.1038/s41467-017-00160-z |
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