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Automated high-throughput light-sheet fluorescence microscopy of larval zebrafish
Light sheet fluorescence microscopy enables fast, minimally phototoxic, three-dimensional imaging of live specimens, but is currently limited by low throughput and tedious sample preparation. Here, we describe an automated high-throughput light sheet fluorescence microscope in which specimens are po...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6235235/ https://www.ncbi.nlm.nih.gov/pubmed/30427839 http://dx.doi.org/10.1371/journal.pone.0198705 |
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author | Logan, Savannah L. Dudley, Christopher Baker, Ryan P. Taormina, Michael J. Hay, Edouard A. Parthasarathy, Raghuveer |
author_facet | Logan, Savannah L. Dudley, Christopher Baker, Ryan P. Taormina, Michael J. Hay, Edouard A. Parthasarathy, Raghuveer |
author_sort | Logan, Savannah L. |
collection | PubMed |
description | Light sheet fluorescence microscopy enables fast, minimally phototoxic, three-dimensional imaging of live specimens, but is currently limited by low throughput and tedious sample preparation. Here, we describe an automated high-throughput light sheet fluorescence microscope in which specimens are positioned by and imaged within a fluidic system integrated with the sheet excitation and detection optics. We demonstrate the ability of the instrument to rapidly examine live specimens with minimal manual intervention by imaging fluorescent neutrophils over a nearly 0.3 mm(3) volume in dozens of larval zebrafish. In addition to revealing considerable inter-individual variability in neutrophil number, known previously from labor-intensive methods, three-dimensional imaging allows assessment of the correlation between the bulk measure of total cellular fluorescence and the spatially resolved measure of actual neutrophil number per animal. We suggest that our simple experimental design should considerably expand the scope and impact of light sheet imaging in the life sciences. |
format | Online Article Text |
id | pubmed-6235235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-62352352018-12-01 Automated high-throughput light-sheet fluorescence microscopy of larval zebrafish Logan, Savannah L. Dudley, Christopher Baker, Ryan P. Taormina, Michael J. Hay, Edouard A. Parthasarathy, Raghuveer PLoS One Research Article Light sheet fluorescence microscopy enables fast, minimally phototoxic, three-dimensional imaging of live specimens, but is currently limited by low throughput and tedious sample preparation. Here, we describe an automated high-throughput light sheet fluorescence microscope in which specimens are positioned by and imaged within a fluidic system integrated with the sheet excitation and detection optics. We demonstrate the ability of the instrument to rapidly examine live specimens with minimal manual intervention by imaging fluorescent neutrophils over a nearly 0.3 mm(3) volume in dozens of larval zebrafish. In addition to revealing considerable inter-individual variability in neutrophil number, known previously from labor-intensive methods, three-dimensional imaging allows assessment of the correlation between the bulk measure of total cellular fluorescence and the spatially resolved measure of actual neutrophil number per animal. We suggest that our simple experimental design should considerably expand the scope and impact of light sheet imaging in the life sciences. Public Library of Science 2018-11-14 /pmc/articles/PMC6235235/ /pubmed/30427839 http://dx.doi.org/10.1371/journal.pone.0198705 Text en © 2018 Logan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Logan, Savannah L. Dudley, Christopher Baker, Ryan P. Taormina, Michael J. Hay, Edouard A. Parthasarathy, Raghuveer Automated high-throughput light-sheet fluorescence microscopy of larval zebrafish |
title | Automated high-throughput light-sheet fluorescence microscopy of larval zebrafish |
title_full | Automated high-throughput light-sheet fluorescence microscopy of larval zebrafish |
title_fullStr | Automated high-throughput light-sheet fluorescence microscopy of larval zebrafish |
title_full_unstemmed | Automated high-throughput light-sheet fluorescence microscopy of larval zebrafish |
title_short | Automated high-throughput light-sheet fluorescence microscopy of larval zebrafish |
title_sort | automated high-throughput light-sheet fluorescence microscopy of larval zebrafish |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6235235/ https://www.ncbi.nlm.nih.gov/pubmed/30427839 http://dx.doi.org/10.1371/journal.pone.0198705 |
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