Simultaneous whole-animal 3D imaging of neuronal activity using light-field microscopy

High-speed, large-scale three-dimensional (3D) imaging of neuronal activity poses a major challenge in neuroscience. Here we demonstrate simultaneous functional imaging of neuronal activity at single-neuron resolution in an entire Caenorhabditis elegans and in larval zebrafish brain. Our technique c...

Full description

Bibliographic Details
Main Authors: Prevedel, Robert, Yoon, Young-Gyu, Hoffmann, Maximilian, Pak, Nikita, Wetzstein, Gordon, Kato, Saul, Schrödel, Tina, Raskar, Ramesh, Zimmer, Manuel, Boyden, Edward Stuart, Vaziri, Alipasha
Other Authors: Massachusetts Institute of Technology. Department of Biological Engineering
Format: Article
Language:en_US
Published: Springer Nature 2016
Online Access:http://hdl.handle.net/1721.1/103551
https://orcid.org/0000-0003-1812-6421
https://orcid.org/0000-0002-2079-0543
https://orcid.org/0000-0002-0419-3351
https://orcid.org/0000-0002-3254-3224
_version_ 1826214643397296128
author Prevedel, Robert
Yoon, Young-Gyu
Hoffmann, Maximilian
Pak, Nikita
Wetzstein, Gordon
Kato, Saul
Schrödel, Tina
Raskar, Ramesh
Zimmer, Manuel
Boyden, Edward Stuart
Vaziri, Alipasha
author2 Massachusetts Institute of Technology. Department of Biological Engineering
author_facet Massachusetts Institute of Technology. Department of Biological Engineering
Prevedel, Robert
Yoon, Young-Gyu
Hoffmann, Maximilian
Pak, Nikita
Wetzstein, Gordon
Kato, Saul
Schrödel, Tina
Raskar, Ramesh
Zimmer, Manuel
Boyden, Edward Stuart
Vaziri, Alipasha
author_sort Prevedel, Robert
collection MIT
description High-speed, large-scale three-dimensional (3D) imaging of neuronal activity poses a major challenge in neuroscience. Here we demonstrate simultaneous functional imaging of neuronal activity at single-neuron resolution in an entire Caenorhabditis elegans and in larval zebrafish brain. Our technique captures the dynamics of spiking neurons in volumes of ~700 μm × 700 μm × 200 μm at 20 Hz. Its simplicity makes it an attractive tool for high-speed volumetric calcium imaging.
first_indexed 2024-09-23T16:08:44Z
format Article
id mit-1721.1/103551
institution Massachusetts Institute of Technology
language en_US
last_indexed 2024-09-23T16:08:44Z
publishDate 2016
publisher Springer Nature
record_format dspace
spelling mit-1721.1/1035512022-09-29T18:34:14Z Simultaneous whole-animal 3D imaging of neuronal activity using light-field microscopy Prevedel, Robert Yoon, Young-Gyu Hoffmann, Maximilian Pak, Nikita Wetzstein, Gordon Kato, Saul Schrödel, Tina Raskar, Ramesh Zimmer, Manuel Boyden, Edward Stuart Vaziri, Alipasha Massachusetts Institute of Technology. Department of Biological Engineering Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences Massachusetts Institute of Technology. Department of Mechanical Engineering Massachusetts Institute of Technology. Media Laboratory McGovern Institute for Brain Research at MIT Yoon, Young-Gyu Pak, Nikita Wetzstein, Gordon Raskar, Ramesh Boyden, Edward Stuart High-speed, large-scale three-dimensional (3D) imaging of neuronal activity poses a major challenge in neuroscience. Here we demonstrate simultaneous functional imaging of neuronal activity at single-neuron resolution in an entire Caenorhabditis elegans and in larval zebrafish brain. Our technique captures the dynamics of spiking neurons in volumes of ~700 μm × 700 μm × 200 μm at 20 Hz. Its simplicity makes it an attractive tool for high-speed volumetric calcium imaging. European Commission (Marie Curie, FP7-PEOPLE-2011-IIF) National Institutes of Health (U.S.) (NIH grant 1R01EY023173) National Science Foundation (U.S.) (NSF CBET 1053233) National Science Foundation (U.S.) (NSF CBET 1344219) National Institutes of Health (U.S.) (NIH 1DP1NS087724) Vienna Science and Technology Fund ((WWTF) project VRG10-11) Seventh Framework Programme (European Commission) (ERC no. 281869) MIT Media Lab Consortium Institution of Engineering and Technology (IET) (Harvey Prize) Human Frontier Science Program (Strasbourg, France) (Project RGP0041/2012) 2016-07-08T16:56:10Z 2016-07-08T16:56:10Z 2014-05 2014-01 Article http://purl.org/eprint/type/JournalArticle 1548-7091 1548-7105 http://hdl.handle.net/1721.1/103551 Prevedel, Robert, Young-Gyu Yoon, Maximilian Hoffmann, Nikita Pak, Gordon Wetzstein, Saul Kato, Tina Schrödel, Ramesh Raskar, Manuel Zimmer, Edward S. Boyden, and Alipasha Vaziri. “Simultaneous Whole-Animal 3D Imaging of Neuronal Activity Using Light-Field Microscopy.” Nature Methods 11, no. 7 (May 18, 2014): 727–730. https://orcid.org/0000-0003-1812-6421 https://orcid.org/0000-0002-2079-0543 https://orcid.org/0000-0002-0419-3351 https://orcid.org/0000-0002-3254-3224 en_US http://dx.doi.org/10.1038/nmeth.2964 Nature Methods Creative Commons Attribution-Noncommercial-Share Alike http://creativecommons.org/licenses/by-nc-sa/4.0/ application/pdf Springer Nature PMC
spellingShingle Prevedel, Robert
Yoon, Young-Gyu
Hoffmann, Maximilian
Pak, Nikita
Wetzstein, Gordon
Kato, Saul
Schrödel, Tina
Raskar, Ramesh
Zimmer, Manuel
Boyden, Edward Stuart
Vaziri, Alipasha
Simultaneous whole-animal 3D imaging of neuronal activity using light-field microscopy
title Simultaneous whole-animal 3D imaging of neuronal activity using light-field microscopy
title_full Simultaneous whole-animal 3D imaging of neuronal activity using light-field microscopy
title_fullStr Simultaneous whole-animal 3D imaging of neuronal activity using light-field microscopy
title_full_unstemmed Simultaneous whole-animal 3D imaging of neuronal activity using light-field microscopy
title_short Simultaneous whole-animal 3D imaging of neuronal activity using light-field microscopy
title_sort simultaneous whole animal 3d imaging of neuronal activity using light field microscopy
url http://hdl.handle.net/1721.1/103551
https://orcid.org/0000-0003-1812-6421
https://orcid.org/0000-0002-2079-0543
https://orcid.org/0000-0002-0419-3351
https://orcid.org/0000-0002-3254-3224
work_keys_str_mv AT prevedelrobert simultaneouswholeanimal3dimagingofneuronalactivityusinglightfieldmicroscopy
AT yoonyounggyu simultaneouswholeanimal3dimagingofneuronalactivityusinglightfieldmicroscopy
AT hoffmannmaximilian simultaneouswholeanimal3dimagingofneuronalactivityusinglightfieldmicroscopy
AT paknikita simultaneouswholeanimal3dimagingofneuronalactivityusinglightfieldmicroscopy
AT wetzsteingordon simultaneouswholeanimal3dimagingofneuronalactivityusinglightfieldmicroscopy
AT katosaul simultaneouswholeanimal3dimagingofneuronalactivityusinglightfieldmicroscopy
AT schrodeltina simultaneouswholeanimal3dimagingofneuronalactivityusinglightfieldmicroscopy
AT raskarramesh simultaneouswholeanimal3dimagingofneuronalactivityusinglightfieldmicroscopy
AT zimmermanuel simultaneouswholeanimal3dimagingofneuronalactivityusinglightfieldmicroscopy
AT boydenedwardstuart simultaneouswholeanimal3dimagingofneuronalactivityusinglightfieldmicroscopy
AT vazirialipasha simultaneouswholeanimal3dimagingofneuronalactivityusinglightfieldmicroscopy