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Simultaneous high-speed imaging and optogenetic inhibition in the intact mouse brain
Genetically encoded calcium indicators and optogenetic actuators can report and manipulate the activity of specific neuronal populations. However, applying imaging and optogenetics simultaneously has been difficult to establish in the mammalian brain, even though combining the techniques would provi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215385/ https://www.ncbi.nlm.nih.gov/pubmed/28053310 http://dx.doi.org/10.1038/srep40041 |
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author | Bovetti, Serena Moretti, Claudio Zucca, Stefano Dal Maschio, Marco Bonifazi, Paolo Fellin, Tommaso |
author_facet | Bovetti, Serena Moretti, Claudio Zucca, Stefano Dal Maschio, Marco Bonifazi, Paolo Fellin, Tommaso |
author_sort | Bovetti, Serena |
collection | PubMed |
description | Genetically encoded calcium indicators and optogenetic actuators can report and manipulate the activity of specific neuronal populations. However, applying imaging and optogenetics simultaneously has been difficult to establish in the mammalian brain, even though combining the techniques would provide a powerful approach to reveal the functional organization of neural circuits. Here, we developed a technique based on patterned two-photon illumination to allow fast scanless imaging of GCaMP6 signals in the intact mouse brain at the same time as single-photon optogenetic inhibition with Archaerhodopsin. Using combined imaging and electrophysiological recording, we demonstrate that single and short bursts of action potentials in pyramidal neurons can be detected in the scanless modality at acquisition frequencies up to 1 kHz. Moreover, we demonstrate that our system strongly reduces the artifacts in the fluorescence detection that are induced by single-photon optogenetic illumination. Finally, we validated our technique investigating the role of parvalbumin-positive (PV) interneurons in the control of spontaneous cortical dynamics. Monitoring the activity of cellular populations on a precise spatiotemporal scale while manipulating neuronal activity with optogenetics provides a powerful tool to causally elucidate the cellular mechanisms underlying circuit function in the intact mammalian brain. |
format | Online Article Text |
id | pubmed-5215385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52153852017-01-09 Simultaneous high-speed imaging and optogenetic inhibition in the intact mouse brain Bovetti, Serena Moretti, Claudio Zucca, Stefano Dal Maschio, Marco Bonifazi, Paolo Fellin, Tommaso Sci Rep Article Genetically encoded calcium indicators and optogenetic actuators can report and manipulate the activity of specific neuronal populations. However, applying imaging and optogenetics simultaneously has been difficult to establish in the mammalian brain, even though combining the techniques would provide a powerful approach to reveal the functional organization of neural circuits. Here, we developed a technique based on patterned two-photon illumination to allow fast scanless imaging of GCaMP6 signals in the intact mouse brain at the same time as single-photon optogenetic inhibition with Archaerhodopsin. Using combined imaging and electrophysiological recording, we demonstrate that single and short bursts of action potentials in pyramidal neurons can be detected in the scanless modality at acquisition frequencies up to 1 kHz. Moreover, we demonstrate that our system strongly reduces the artifacts in the fluorescence detection that are induced by single-photon optogenetic illumination. Finally, we validated our technique investigating the role of parvalbumin-positive (PV) interneurons in the control of spontaneous cortical dynamics. Monitoring the activity of cellular populations on a precise spatiotemporal scale while manipulating neuronal activity with optogenetics provides a powerful tool to causally elucidate the cellular mechanisms underlying circuit function in the intact mammalian brain. Nature Publishing Group 2017-01-05 /pmc/articles/PMC5215385/ /pubmed/28053310 http://dx.doi.org/10.1038/srep40041 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Bovetti, Serena Moretti, Claudio Zucca, Stefano Dal Maschio, Marco Bonifazi, Paolo Fellin, Tommaso Simultaneous high-speed imaging and optogenetic inhibition in the intact mouse brain |
title | Simultaneous high-speed imaging and optogenetic inhibition in the intact mouse brain |
title_full | Simultaneous high-speed imaging and optogenetic inhibition in the intact mouse brain |
title_fullStr | Simultaneous high-speed imaging and optogenetic inhibition in the intact mouse brain |
title_full_unstemmed | Simultaneous high-speed imaging and optogenetic inhibition in the intact mouse brain |
title_short | Simultaneous high-speed imaging and optogenetic inhibition in the intact mouse brain |
title_sort | simultaneous high-speed imaging and optogenetic inhibition in the intact mouse brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215385/ https://www.ncbi.nlm.nih.gov/pubmed/28053310 http://dx.doi.org/10.1038/srep40041 |
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