Simultaneous two-photon imaging and two-photon optogenetics of cortical circuits in three dimensions

The simultaneous imaging and manipulating of neural activity could enable the functional dissection of neural circuits. Here we have combined two-photon optogenetics with simultaneous volumetric two-photon calcium imaging to measure and manipulate neural activity in mouse neocortex in vivo in three-...

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Main Authors: Weijian Yang, Luis Carrillo-Reid, Yuki Bando, Darcy S Peterka, Rafael Yuste
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2018-02-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/32671
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spelling doaj-5405d31bc61c4404af680d0c7a243d252021-05-05T15:35:24ZengeLife Sciences Publications LtdeLife2050-084X2018-02-01710.7554/eLife.32671Simultaneous two-photon imaging and two-photon optogenetics of cortical circuits in three dimensionsWeijian Yang0https://orcid.org/0000-0003-0941-3496Luis Carrillo-Reid1Yuki Bando2Darcy S Peterka3https://orcid.org/0000-0001-7351-5820Rafael Yuste4https://orcid.org/0000-0003-4206-497XNeuroTechnology Center, Department of Biological Sciences, Columbia University, New York, United StatesNeuroTechnology Center, Department of Biological Sciences, Columbia University, New York, United StatesNeuroTechnology Center, Department of Biological Sciences, Columbia University, New York, United StatesNeuroTechnology Center, Department of Biological Sciences, Columbia University, New York, United StatesNeuroTechnology Center, Department of Biological Sciences, Columbia University, New York, United StatesThe simultaneous imaging and manipulating of neural activity could enable the functional dissection of neural circuits. Here we have combined two-photon optogenetics with simultaneous volumetric two-photon calcium imaging to measure and manipulate neural activity in mouse neocortex in vivo in three-dimensions (3D) with cellular resolution. Using a hybrid holographic approach, we simultaneously photostimulate more than 80 neurons over 150 μm in depth in layer 2/3 of the mouse visual cortex, while simultaneously imaging the activity of the surrounding neurons. We validate the usefulness of the method by photoactivating in 3D selected groups of interneurons, suppressing the response of nearby pyramidal neurons to visual stimuli in awake animals. Our all-optical approach could be used as a general platform to read and write neuronal activity.https://elifesciences.org/articles/32671optogeneticstwo-photoncalcium imagingthree-dimensionalholographicvolumetric
collection DOAJ
language English
format Article
sources DOAJ
author Weijian Yang
Luis Carrillo-Reid
Yuki Bando
Darcy S Peterka
Rafael Yuste
spellingShingle Weijian Yang
Luis Carrillo-Reid
Yuki Bando
Darcy S Peterka
Rafael Yuste
Simultaneous two-photon imaging and two-photon optogenetics of cortical circuits in three dimensions
eLife
optogenetics
two-photon
calcium imaging
three-dimensional
holographic
volumetric
author_facet Weijian Yang
Luis Carrillo-Reid
Yuki Bando
Darcy S Peterka
Rafael Yuste
author_sort Weijian Yang
title Simultaneous two-photon imaging and two-photon optogenetics of cortical circuits in three dimensions
title_short Simultaneous two-photon imaging and two-photon optogenetics of cortical circuits in three dimensions
title_full Simultaneous two-photon imaging and two-photon optogenetics of cortical circuits in three dimensions
title_fullStr Simultaneous two-photon imaging and two-photon optogenetics of cortical circuits in three dimensions
title_full_unstemmed Simultaneous two-photon imaging and two-photon optogenetics of cortical circuits in three dimensions
title_sort simultaneous two-photon imaging and two-photon optogenetics of cortical circuits in three dimensions
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2018-02-01
description The simultaneous imaging and manipulating of neural activity could enable the functional dissection of neural circuits. Here we have combined two-photon optogenetics with simultaneous volumetric two-photon calcium imaging to measure and manipulate neural activity in mouse neocortex in vivo in three-dimensions (3D) with cellular resolution. Using a hybrid holographic approach, we simultaneously photostimulate more than 80 neurons over 150 μm in depth in layer 2/3 of the mouse visual cortex, while simultaneously imaging the activity of the surrounding neurons. We validate the usefulness of the method by photoactivating in 3D selected groups of interneurons, suppressing the response of nearby pyramidal neurons to visual stimuli in awake animals. Our all-optical approach could be used as a general platform to read and write neuronal activity.
topic optogenetics
two-photon
calcium imaging
three-dimensional
holographic
volumetric
url https://elifesciences.org/articles/32671
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