Cargando…

Three-dimensional scanless holographic optogenetics with temporal focusing (3D-SHOT)

Optical methods capable of manipulating neural activity with cellular resolution and millisecond precision in three dimensions will accelerate the pace of neuroscience research. Existing approaches for targeting individual neurons, however, fall short of these requirements. Here we present a new mul...

Descripción completa

Detalles Bibliográficos
Autores principales: Pégard, Nicolas C., Mardinly, Alan R., Oldenburg, Ian Antón, Sridharan, Savitha, Waller, Laura, Adesnik, Hillel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663714/
https://www.ncbi.nlm.nih.gov/pubmed/29089483
http://dx.doi.org/10.1038/s41467-017-01031-3
_version_ 1783274864269852672
author Pégard, Nicolas C.
Mardinly, Alan R.
Oldenburg, Ian Antón
Sridharan, Savitha
Waller, Laura
Adesnik, Hillel
author_facet Pégard, Nicolas C.
Mardinly, Alan R.
Oldenburg, Ian Antón
Sridharan, Savitha
Waller, Laura
Adesnik, Hillel
author_sort Pégard, Nicolas C.
collection PubMed
description Optical methods capable of manipulating neural activity with cellular resolution and millisecond precision in three dimensions will accelerate the pace of neuroscience research. Existing approaches for targeting individual neurons, however, fall short of these requirements. Here we present a new multiphoton photo-excitation method, termed three-dimensional scanless holographic optogenetics with temporal focusing (3D-SHOT), which allows precise, simultaneous photo-activation of arbitrary sets of neurons anywhere within the addressable volume of a microscope. This technique uses point-cloud holography to place multiple copies of a temporally focused disc matching the dimensions of a neuron’s cell body. Experiments in cultured cells, brain slices, and in living mice demonstrate single-neuron spatial resolution even when optically targeting randomly distributed groups of neurons in 3D. This approach opens new avenues for mapping and manipulating neural circuits, allowing a real-time, cellular resolution interface to the brain.
format Online
Article
Text
id pubmed-5663714
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-56637142017-11-02 Three-dimensional scanless holographic optogenetics with temporal focusing (3D-SHOT) Pégard, Nicolas C. Mardinly, Alan R. Oldenburg, Ian Antón Sridharan, Savitha Waller, Laura Adesnik, Hillel Nat Commun Article Optical methods capable of manipulating neural activity with cellular resolution and millisecond precision in three dimensions will accelerate the pace of neuroscience research. Existing approaches for targeting individual neurons, however, fall short of these requirements. Here we present a new multiphoton photo-excitation method, termed three-dimensional scanless holographic optogenetics with temporal focusing (3D-SHOT), which allows precise, simultaneous photo-activation of arbitrary sets of neurons anywhere within the addressable volume of a microscope. This technique uses point-cloud holography to place multiple copies of a temporally focused disc matching the dimensions of a neuron’s cell body. Experiments in cultured cells, brain slices, and in living mice demonstrate single-neuron spatial resolution even when optically targeting randomly distributed groups of neurons in 3D. This approach opens new avenues for mapping and manipulating neural circuits, allowing a real-time, cellular resolution interface to the brain. Nature Publishing Group UK 2017-10-31 /pmc/articles/PMC5663714/ /pubmed/29089483 http://dx.doi.org/10.1038/s41467-017-01031-3 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
Pégard, Nicolas C.
Mardinly, Alan R.
Oldenburg, Ian Antón
Sridharan, Savitha
Waller, Laura
Adesnik, Hillel
Three-dimensional scanless holographic optogenetics with temporal focusing (3D-SHOT)
title Three-dimensional scanless holographic optogenetics with temporal focusing (3D-SHOT)
title_full Three-dimensional scanless holographic optogenetics with temporal focusing (3D-SHOT)
title_fullStr Three-dimensional scanless holographic optogenetics with temporal focusing (3D-SHOT)
title_full_unstemmed Three-dimensional scanless holographic optogenetics with temporal focusing (3D-SHOT)
title_short Three-dimensional scanless holographic optogenetics with temporal focusing (3D-SHOT)
title_sort three-dimensional scanless holographic optogenetics with temporal focusing (3d-shot)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663714/
https://www.ncbi.nlm.nih.gov/pubmed/29089483
http://dx.doi.org/10.1038/s41467-017-01031-3
work_keys_str_mv AT pegardnicolasc threedimensionalscanlessholographicoptogeneticswithtemporalfocusing3dshot
AT mardinlyalanr threedimensionalscanlessholographicoptogeneticswithtemporalfocusing3dshot
AT oldenburgiananton threedimensionalscanlessholographicoptogeneticswithtemporalfocusing3dshot
AT sridharansavitha threedimensionalscanlessholographicoptogeneticswithtemporalfocusing3dshot
AT wallerlaura threedimensionalscanlessholographicoptogeneticswithtemporalfocusing3dshot
AT adesnikhillel threedimensionalscanlessholographicoptogeneticswithtemporalfocusing3dshot