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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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 |
work_keys_str_mv |
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