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Light-Sheet Fluorescence Microscopy with Scanning Non-diffracting Beams
Light-sheet fluorescence microscopy (LSFM) has now become a unique tool in different fields ranging from three-dimensional (3D) tissue imaging to real-time functional imaging of neuronal activities. Nevertheless, obtaining high-quality artifact-free images from large, dense and inhomogeneous samples...
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/PMC7244762/ https://www.ncbi.nlm.nih.gov/pubmed/32444603 http://dx.doi.org/10.1038/s41598-020-63847-2 |
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author | Kafian, Hosein Lalenejad, Meelad Moradi-Mehr, Sahar Birgani, Shiva Akbari Abdollahpour, Daryoush |
author_facet | Kafian, Hosein Lalenejad, Meelad Moradi-Mehr, Sahar Birgani, Shiva Akbari Abdollahpour, Daryoush |
author_sort | Kafian, Hosein |
collection | PubMed |
description | Light-sheet fluorescence microscopy (LSFM) has now become a unique tool in different fields ranging from three-dimensional (3D) tissue imaging to real-time functional imaging of neuronal activities. Nevertheless, obtaining high-quality artifact-free images from large, dense and inhomogeneous samples is the main challenge of the method that still needs to be adequately addressed. Here, we demonstrate significant enhancement of LSFM image qualities by using scanning non-diffracting illuminating beams, both through experimental and numerical investigations. The effect of static and scanning illumination with several beams are analyzed and compared, and it is shown that scanning 2D Airy light-sheet is minimally affected by the inhomogeneities in the samples, and provides higher contrasts and uniform resolution over a wide field-of-view, due to its reduced spatial coherence, self-healing feature and longer penetration depth. Further, the capabilities of the illumination scheme is utilized for both single-and double-wavelength 3D imaging of large and dense mammospheres of cancer tumor cells as complex inhomogeneous biological samples. |
format | Online Article Text |
id | pubmed-7244762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72447622020-05-30 Light-Sheet Fluorescence Microscopy with Scanning Non-diffracting Beams Kafian, Hosein Lalenejad, Meelad Moradi-Mehr, Sahar Birgani, Shiva Akbari Abdollahpour, Daryoush Sci Rep Article Light-sheet fluorescence microscopy (LSFM) has now become a unique tool in different fields ranging from three-dimensional (3D) tissue imaging to real-time functional imaging of neuronal activities. Nevertheless, obtaining high-quality artifact-free images from large, dense and inhomogeneous samples is the main challenge of the method that still needs to be adequately addressed. Here, we demonstrate significant enhancement of LSFM image qualities by using scanning non-diffracting illuminating beams, both through experimental and numerical investigations. The effect of static and scanning illumination with several beams are analyzed and compared, and it is shown that scanning 2D Airy light-sheet is minimally affected by the inhomogeneities in the samples, and provides higher contrasts and uniform resolution over a wide field-of-view, due to its reduced spatial coherence, self-healing feature and longer penetration depth. Further, the capabilities of the illumination scheme is utilized for both single-and double-wavelength 3D imaging of large and dense mammospheres of cancer tumor cells as complex inhomogeneous biological samples. Nature Publishing Group UK 2020-05-22 /pmc/articles/PMC7244762/ /pubmed/32444603 http://dx.doi.org/10.1038/s41598-020-63847-2 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Kafian, Hosein Lalenejad, Meelad Moradi-Mehr, Sahar Birgani, Shiva Akbari Abdollahpour, Daryoush Light-Sheet Fluorescence Microscopy with Scanning Non-diffracting Beams |
title | Light-Sheet Fluorescence Microscopy with Scanning Non-diffracting Beams |
title_full | Light-Sheet Fluorescence Microscopy with Scanning Non-diffracting Beams |
title_fullStr | Light-Sheet Fluorescence Microscopy with Scanning Non-diffracting Beams |
title_full_unstemmed | Light-Sheet Fluorescence Microscopy with Scanning Non-diffracting Beams |
title_short | Light-Sheet Fluorescence Microscopy with Scanning Non-diffracting Beams |
title_sort | light-sheet fluorescence microscopy with scanning non-diffracting beams |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244762/ https://www.ncbi.nlm.nih.gov/pubmed/32444603 http://dx.doi.org/10.1038/s41598-020-63847-2 |
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