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High-Fidelity Imaging in Brain-Wide Structural Studies Using Light-Sheet Microscopy
Light-sheet microscopy (LSM) has proven a useful tool in neuroscience to image whole brains with high frame rates at cellular resolution and, in combination with tissue clearing methods, is often employed to reconstruct the cyto-architecture over the intact mouse brain. Inherently to LSM, however, r...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325532/ https://www.ncbi.nlm.nih.gov/pubmed/30627630 http://dx.doi.org/10.1523/ENEURO.0124-18.2018 |
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author | Müllenbroich, M. Caroline Silvestri, Ludovico Di Giovanna, Antonino P. Mazzamuto, Giacomo Costantini, Irene Sacconi, Leonardo Pavone, Francesco S. |
author_facet | Müllenbroich, M. Caroline Silvestri, Ludovico Di Giovanna, Antonino P. Mazzamuto, Giacomo Costantini, Irene Sacconi, Leonardo Pavone, Francesco S. |
author_sort | Müllenbroich, M. Caroline |
collection | PubMed |
description | Light-sheet microscopy (LSM) has proven a useful tool in neuroscience to image whole brains with high frame rates at cellular resolution and, in combination with tissue clearing methods, is often employed to reconstruct the cyto-architecture over the intact mouse brain. Inherently to LSM, however, residual opaque objects, always present to some extent even in extremely well optically cleared samples, cause stripe artifacts, which, in the best case, severely affect image homogeneity and, in the worst case, completely obscure features of interest. Here, demonstrating two example applications in intact optically cleared mouse brains, we report how Bessel beams reduce streaking artifacts and produce high-fidelity structural data for the brain-wide morphology of neuronal and vascular networks. We found that a third of the imaged volume of the brain was affected by strong striated image intensity inhomogeneity and, furthermore, a significant amount of information content lost with Gaussian illumination was accessible when interrogated with Bessel beams. In conclusion, Bessel beams produce high-fidelity structural data of improved image homogeneity and might significantly relax demands placed on the automated tools to count, trace, or segment fluorescent features of interest. |
format | Online Article Text |
id | pubmed-6325532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-63255322019-01-09 High-Fidelity Imaging in Brain-Wide Structural Studies Using Light-Sheet Microscopy Müllenbroich, M. Caroline Silvestri, Ludovico Di Giovanna, Antonino P. Mazzamuto, Giacomo Costantini, Irene Sacconi, Leonardo Pavone, Francesco S. eNeuro Methods/New Tools Light-sheet microscopy (LSM) has proven a useful tool in neuroscience to image whole brains with high frame rates at cellular resolution and, in combination with tissue clearing methods, is often employed to reconstruct the cyto-architecture over the intact mouse brain. Inherently to LSM, however, residual opaque objects, always present to some extent even in extremely well optically cleared samples, cause stripe artifacts, which, in the best case, severely affect image homogeneity and, in the worst case, completely obscure features of interest. Here, demonstrating two example applications in intact optically cleared mouse brains, we report how Bessel beams reduce streaking artifacts and produce high-fidelity structural data for the brain-wide morphology of neuronal and vascular networks. We found that a third of the imaged volume of the brain was affected by strong striated image intensity inhomogeneity and, furthermore, a significant amount of information content lost with Gaussian illumination was accessible when interrogated with Bessel beams. In conclusion, Bessel beams produce high-fidelity structural data of improved image homogeneity and might significantly relax demands placed on the automated tools to count, trace, or segment fluorescent features of interest. Society for Neuroscience 2018-11-22 /pmc/articles/PMC6325532/ /pubmed/30627630 http://dx.doi.org/10.1523/ENEURO.0124-18.2018 Text en Copyright © 2018 Müllenbroich et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Methods/New Tools Müllenbroich, M. Caroline Silvestri, Ludovico Di Giovanna, Antonino P. Mazzamuto, Giacomo Costantini, Irene Sacconi, Leonardo Pavone, Francesco S. High-Fidelity Imaging in Brain-Wide Structural Studies Using Light-Sheet Microscopy |
title | High-Fidelity Imaging in Brain-Wide Structural Studies Using Light-Sheet Microscopy |
title_full | High-Fidelity Imaging in Brain-Wide Structural Studies Using Light-Sheet Microscopy |
title_fullStr | High-Fidelity Imaging in Brain-Wide Structural Studies Using Light-Sheet Microscopy |
title_full_unstemmed | High-Fidelity Imaging in Brain-Wide Structural Studies Using Light-Sheet Microscopy |
title_short | High-Fidelity Imaging in Brain-Wide Structural Studies Using Light-Sheet Microscopy |
title_sort | high-fidelity imaging in brain-wide structural studies using light-sheet microscopy |
topic | Methods/New Tools |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325532/ https://www.ncbi.nlm.nih.gov/pubmed/30627630 http://dx.doi.org/10.1523/ENEURO.0124-18.2018 |
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