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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7021898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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