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High-contrast, synchronous volumetric imaging with selective volume illumination microscopy

Light-field fluorescence microscopy uniquely provides fast, synchronous volumetric imaging by capturing an extended volume in one snapshot, but often suffers from low contrast due to the background signal generated by its wide-field illumination strategy. We implemented light-field-based selective v...

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Autores principales: Truong, Thai V., Holland, Daniel B., Madaan, Sara, Andreev, Andrey, Keomanee-Dizon, Kevin, Troll, Josh V., Koo, Daniel E. S., McFall-Ngai, Margaret J., Fraser, Scott E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021898/
https://www.ncbi.nlm.nih.gov/pubmed/32060411
http://dx.doi.org/10.1038/s42003-020-0787-6
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author Truong, Thai V.
Holland, Daniel B.
Madaan, Sara
Andreev, Andrey
Keomanee-Dizon, Kevin
Troll, Josh V.
Koo, Daniel E. S.
McFall-Ngai, Margaret J.
Fraser, Scott E.
author_facet Truong, Thai V.
Holland, Daniel B.
Madaan, Sara
Andreev, Andrey
Keomanee-Dizon, Kevin
Troll, Josh V.
Koo, Daniel E. S.
McFall-Ngai, Margaret J.
Fraser, Scott E.
author_sort Truong, Thai V.
collection PubMed
description Light-field fluorescence microscopy uniquely provides fast, synchronous volumetric imaging by capturing an extended volume in one snapshot, but often suffers from low contrast due to the background signal generated by its wide-field illumination strategy. We implemented light-field-based selective volume illumination microscopy (SVIM), where illumination is confined to only the volume of interest, removing the background generated from the extraneous sample volume, and dramatically enhancing the image contrast. We demonstrate the capabilities of SVIM by capturing cellular-resolution 3D movies of flowing bacteria in seawater as they colonize their squid symbiotic partner, as well as of the beating heart and brain-wide neural activity in larval zebrafish. These applications demonstrate the breadth of imaging applications that we envision SVIM will enable, in capturing tissue-scale 3D dynamic biological systems at single-cell resolution, fast volumetric rates, and high contrast to reveal the underlying biology.
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spelling pubmed-70218982020-03-03 High-contrast, synchronous volumetric imaging with selective volume illumination microscopy Truong, Thai V. Holland, Daniel B. Madaan, Sara Andreev, Andrey Keomanee-Dizon, Kevin Troll, Josh V. Koo, Daniel E. S. McFall-Ngai, Margaret J. Fraser, Scott E. Commun Biol Article Light-field fluorescence microscopy uniquely provides fast, synchronous volumetric imaging by capturing an extended volume in one snapshot, but often suffers from low contrast due to the background signal generated by its wide-field illumination strategy. We implemented light-field-based selective volume illumination microscopy (SVIM), where illumination is confined to only the volume of interest, removing the background generated from the extraneous sample volume, and dramatically enhancing the image contrast. We demonstrate the capabilities of SVIM by capturing cellular-resolution 3D movies of flowing bacteria in seawater as they colonize their squid symbiotic partner, as well as of the beating heart and brain-wide neural activity in larval zebrafish. These applications demonstrate the breadth of imaging applications that we envision SVIM will enable, in capturing tissue-scale 3D dynamic biological systems at single-cell resolution, fast volumetric rates, and high contrast to reveal the underlying biology. Nature Publishing Group UK 2020-02-14 /pmc/articles/PMC7021898/ /pubmed/32060411 http://dx.doi.org/10.1038/s42003-020-0787-6 Text en © The Author(s) 2020, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Truong, Thai V.
Holland, Daniel B.
Madaan, Sara
Andreev, Andrey
Keomanee-Dizon, Kevin
Troll, Josh V.
Koo, Daniel E. S.
McFall-Ngai, Margaret J.
Fraser, Scott E.
High-contrast, synchronous volumetric imaging with selective volume illumination microscopy
title High-contrast, synchronous volumetric imaging with selective volume illumination microscopy
title_full High-contrast, synchronous volumetric imaging with selective volume illumination microscopy
title_fullStr High-contrast, synchronous volumetric imaging with selective volume illumination microscopy
title_full_unstemmed High-contrast, synchronous volumetric imaging with selective volume illumination microscopy
title_short High-contrast, synchronous volumetric imaging with selective volume illumination microscopy
title_sort high-contrast, synchronous volumetric imaging with selective volume illumination microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021898/
https://www.ncbi.nlm.nih.gov/pubmed/32060411
http://dx.doi.org/10.1038/s42003-020-0787-6
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