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Comparison of Multiscale Imaging Methods for Brain Research

A major challenge in neuroscience is how to study structural alterations in the brain. Even small changes in synaptic composition could have severe outcomes for body functions. Many neuropathological diseases are attributable to disorganization of particular synaptic proteins. Yet, to detect and com...

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Autores principales: Tröger, Jessica, Hoischen, Christian, Perner, Birgit, Monajembashi, Shamci, Barbotin, Aurélien, Löschberger, Anna, Eggeling, Christian, Kessels, Michael M., Qualmann, Britta, Hemmerich, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349602/
https://www.ncbi.nlm.nih.gov/pubmed/32492970
http://dx.doi.org/10.3390/cells9061377
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author Tröger, Jessica
Hoischen, Christian
Perner, Birgit
Monajembashi, Shamci
Barbotin, Aurélien
Löschberger, Anna
Eggeling, Christian
Kessels, Michael M.
Qualmann, Britta
Hemmerich, Peter
author_facet Tröger, Jessica
Hoischen, Christian
Perner, Birgit
Monajembashi, Shamci
Barbotin, Aurélien
Löschberger, Anna
Eggeling, Christian
Kessels, Michael M.
Qualmann, Britta
Hemmerich, Peter
author_sort Tröger, Jessica
collection PubMed
description A major challenge in neuroscience is how to study structural alterations in the brain. Even small changes in synaptic composition could have severe outcomes for body functions. Many neuropathological diseases are attributable to disorganization of particular synaptic proteins. Yet, to detect and comprehensively describe and evaluate such often rather subtle deviations from the normal physiological status in a detailed and quantitative manner is very challenging. Here, we have compared side-by-side several commercially available light microscopes for their suitability in visualizing synaptic components in larger parts of the brain at low resolution, at extended resolution as well as at super-resolution. Microscopic technologies included stereo, widefield, deconvolution, confocal, and super-resolution set-ups. We also analyzed the impact of adaptive optics, a motorized objective correction collar and CUDA graphics card technology on imaging quality and acquisition speed. Our observations evaluate a basic set of techniques, which allow for multi-color brain imaging from centimeter to nanometer scales. The comparative multi-modal strategy we established can be used as a guide for researchers to select the most appropriate light microscopy method in addressing specific questions in brain research, and we also give insights into recent developments such as optical aberration corrections.
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spelling pubmed-73496022020-07-14 Comparison of Multiscale Imaging Methods for Brain Research Tröger, Jessica Hoischen, Christian Perner, Birgit Monajembashi, Shamci Barbotin, Aurélien Löschberger, Anna Eggeling, Christian Kessels, Michael M. Qualmann, Britta Hemmerich, Peter Cells Article A major challenge in neuroscience is how to study structural alterations in the brain. Even small changes in synaptic composition could have severe outcomes for body functions. Many neuropathological diseases are attributable to disorganization of particular synaptic proteins. Yet, to detect and comprehensively describe and evaluate such often rather subtle deviations from the normal physiological status in a detailed and quantitative manner is very challenging. Here, we have compared side-by-side several commercially available light microscopes for their suitability in visualizing synaptic components in larger parts of the brain at low resolution, at extended resolution as well as at super-resolution. Microscopic technologies included stereo, widefield, deconvolution, confocal, and super-resolution set-ups. We also analyzed the impact of adaptive optics, a motorized objective correction collar and CUDA graphics card technology on imaging quality and acquisition speed. Our observations evaluate a basic set of techniques, which allow for multi-color brain imaging from centimeter to nanometer scales. The comparative multi-modal strategy we established can be used as a guide for researchers to select the most appropriate light microscopy method in addressing specific questions in brain research, and we also give insights into recent developments such as optical aberration corrections. MDPI 2020-06-01 /pmc/articles/PMC7349602/ /pubmed/32492970 http://dx.doi.org/10.3390/cells9061377 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tröger, Jessica
Hoischen, Christian
Perner, Birgit
Monajembashi, Shamci
Barbotin, Aurélien
Löschberger, Anna
Eggeling, Christian
Kessels, Michael M.
Qualmann, Britta
Hemmerich, Peter
Comparison of Multiscale Imaging Methods for Brain Research
title Comparison of Multiscale Imaging Methods for Brain Research
title_full Comparison of Multiscale Imaging Methods for Brain Research
title_fullStr Comparison of Multiscale Imaging Methods for Brain Research
title_full_unstemmed Comparison of Multiscale Imaging Methods for Brain Research
title_short Comparison of Multiscale Imaging Methods for Brain Research
title_sort comparison of multiscale imaging methods for brain research
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349602/
https://www.ncbi.nlm.nih.gov/pubmed/32492970
http://dx.doi.org/10.3390/cells9061377
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