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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...

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Detalles Bibliográficos
Autores principales: Logan, Savannah L., Dudley, Christopher, Baker, Ryan P., Taormina, Michael J., Hay, Edouard A., Parthasarathy, Raghuveer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
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.
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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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