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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...

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Autores principales: Bovetti, Serena, Moretti, Claudio, Zucca, Stefano, Dal Maschio, Marco, Bonifazi, Paolo, Fellin, Tommaso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
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.
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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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