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Flexible Multi-Beam Light-Sheet Fluorescence Microscope for Live Imaging Without Striping Artifacts
The development of light-sheet fluorescence microscopy (LSFM) has greatly expanded the experimental capabilities in many biological and biomedical research fields, enabling for example live studies of murine and zebrafish neural activity or of cell growth and division. The key feature of the method...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376877/ https://www.ncbi.nlm.nih.gov/pubmed/30800060 http://dx.doi.org/10.3389/fnana.2019.00007 |
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author | Sancataldo, Giuseppe Gavryusev, Vladislav de Vito, Giuseppe Turrini, Lapo Locatelli, Massimiliano Fornetto, Chiara Tiso, Natascia Vanzi, Francesco Silvestri, Ludovico Pavone, Francesco Saverio |
author_facet | Sancataldo, Giuseppe Gavryusev, Vladislav de Vito, Giuseppe Turrini, Lapo Locatelli, Massimiliano Fornetto, Chiara Tiso, Natascia Vanzi, Francesco Silvestri, Ludovico Pavone, Francesco Saverio |
author_sort | Sancataldo, Giuseppe |
collection | PubMed |
description | The development of light-sheet fluorescence microscopy (LSFM) has greatly expanded the experimental capabilities in many biological and biomedical research fields, enabling for example live studies of murine and zebrafish neural activity or of cell growth and division. The key feature of the method is the selective illumination of a sample single plane, providing an intrinsic optical sectioning and allowing direct 2D image recording. On the other hand, this excitation scheme is more affected by absorption or scattering artifacts in comparison to point scanning methods, leading to un-even illumination. We present here an easily implementable method, based on acousto-optical deflectors (AOD), to overcome this obstacle. We report the advantages provided by flexible and fast AODs in generating simultaneous angled multiple beams from a single laser beam and in fast light sheet pivoting and we demonstrate the suppression of illumination artifacts. |
format | Online Article Text |
id | pubmed-6376877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63768772019-02-22 Flexible Multi-Beam Light-Sheet Fluorescence Microscope for Live Imaging Without Striping Artifacts Sancataldo, Giuseppe Gavryusev, Vladislav de Vito, Giuseppe Turrini, Lapo Locatelli, Massimiliano Fornetto, Chiara Tiso, Natascia Vanzi, Francesco Silvestri, Ludovico Pavone, Francesco Saverio Front Neuroanat Neuroscience The development of light-sheet fluorescence microscopy (LSFM) has greatly expanded the experimental capabilities in many biological and biomedical research fields, enabling for example live studies of murine and zebrafish neural activity or of cell growth and division. The key feature of the method is the selective illumination of a sample single plane, providing an intrinsic optical sectioning and allowing direct 2D image recording. On the other hand, this excitation scheme is more affected by absorption or scattering artifacts in comparison to point scanning methods, leading to un-even illumination. We present here an easily implementable method, based on acousto-optical deflectors (AOD), to overcome this obstacle. We report the advantages provided by flexible and fast AODs in generating simultaneous angled multiple beams from a single laser beam and in fast light sheet pivoting and we demonstrate the suppression of illumination artifacts. Frontiers Media S.A. 2019-02-08 /pmc/articles/PMC6376877/ /pubmed/30800060 http://dx.doi.org/10.3389/fnana.2019.00007 Text en Copyright © 2019 Sancataldo, Gavryusev, de Vito, Turrini, Locatelli, Fornetto, Tiso, Vanzi, Silvestri and Pavone. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Sancataldo, Giuseppe Gavryusev, Vladislav de Vito, Giuseppe Turrini, Lapo Locatelli, Massimiliano Fornetto, Chiara Tiso, Natascia Vanzi, Francesco Silvestri, Ludovico Pavone, Francesco Saverio Flexible Multi-Beam Light-Sheet Fluorescence Microscope for Live Imaging Without Striping Artifacts |
title | Flexible Multi-Beam Light-Sheet Fluorescence Microscope for Live Imaging Without Striping Artifacts |
title_full | Flexible Multi-Beam Light-Sheet Fluorescence Microscope for Live Imaging Without Striping Artifacts |
title_fullStr | Flexible Multi-Beam Light-Sheet Fluorescence Microscope for Live Imaging Without Striping Artifacts |
title_full_unstemmed | Flexible Multi-Beam Light-Sheet Fluorescence Microscope for Live Imaging Without Striping Artifacts |
title_short | Flexible Multi-Beam Light-Sheet Fluorescence Microscope for Live Imaging Without Striping Artifacts |
title_sort | flexible multi-beam light-sheet fluorescence microscope for live imaging without striping artifacts |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376877/ https://www.ncbi.nlm.nih.gov/pubmed/30800060 http://dx.doi.org/10.3389/fnana.2019.00007 |
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