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Expansion Light Sheet Microscopy Resolves Subcellular Structures in Large Portions of the Songbird Brain
Expansion microscopy and light sheet imaging (ExLSM) provide a viable alternative to existing tissue clearing and large volume imaging approaches. The analysis of intact volumes of brain tissue presents a distinct challenge in neuroscience. Recent advances in tissue clearing and light sheet microsco...
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/PMC6365838/ https://www.ncbi.nlm.nih.gov/pubmed/30766480 http://dx.doi.org/10.3389/fnana.2019.00002 |
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author | Düring, Daniel Normen Rocha, Mariana Diales Dittrich, Falk Gahr, Manfred Hahnloser, Richard Hans Robert |
author_facet | Düring, Daniel Normen Rocha, Mariana Diales Dittrich, Falk Gahr, Manfred Hahnloser, Richard Hans Robert |
author_sort | Düring, Daniel Normen |
collection | PubMed |
description | Expansion microscopy and light sheet imaging (ExLSM) provide a viable alternative to existing tissue clearing and large volume imaging approaches. The analysis of intact volumes of brain tissue presents a distinct challenge in neuroscience. Recent advances in tissue clearing and light sheet microscopy have re-addressed this challenge and blossomed into a plethora of protocols with diverse advantages and disadvantages. While refractive index matching achieves near perfect transparency and allows for imaging at large depths, the resolution of cleared brains is usually limited to the micrometer range. Moreover, the often long and harsh tissue clearing protocols hinder preservation of native fluorescence and antigenicity. Here we image large expanded brain volumes of zebra finch brain tissue in commercially available light sheet microscopes. Our expansion light sheet microscopy (ExLSM) approach presents a viable alternative to many clearing and imaging methods because it improves on tissue processing times, fluorophore compatibility, and image resolution. |
format | Online Article Text |
id | pubmed-6365838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63658382019-02-14 Expansion Light Sheet Microscopy Resolves Subcellular Structures in Large Portions of the Songbird Brain Düring, Daniel Normen Rocha, Mariana Diales Dittrich, Falk Gahr, Manfred Hahnloser, Richard Hans Robert Front Neuroanat Neuroscience Expansion microscopy and light sheet imaging (ExLSM) provide a viable alternative to existing tissue clearing and large volume imaging approaches. The analysis of intact volumes of brain tissue presents a distinct challenge in neuroscience. Recent advances in tissue clearing and light sheet microscopy have re-addressed this challenge and blossomed into a plethora of protocols with diverse advantages and disadvantages. While refractive index matching achieves near perfect transparency and allows for imaging at large depths, the resolution of cleared brains is usually limited to the micrometer range. Moreover, the often long and harsh tissue clearing protocols hinder preservation of native fluorescence and antigenicity. Here we image large expanded brain volumes of zebra finch brain tissue in commercially available light sheet microscopes. Our expansion light sheet microscopy (ExLSM) approach presents a viable alternative to many clearing and imaging methods because it improves on tissue processing times, fluorophore compatibility, and image resolution. Frontiers Media S.A. 2019-01-31 /pmc/articles/PMC6365838/ /pubmed/30766480 http://dx.doi.org/10.3389/fnana.2019.00002 Text en Copyright © 2019 Düring, Rocha, Dittrich, Gahr and Hahnloser. http://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 Düring, Daniel Normen Rocha, Mariana Diales Dittrich, Falk Gahr, Manfred Hahnloser, Richard Hans Robert Expansion Light Sheet Microscopy Resolves Subcellular Structures in Large Portions of the Songbird Brain |
title | Expansion Light Sheet Microscopy Resolves Subcellular Structures in Large Portions of the Songbird Brain |
title_full | Expansion Light Sheet Microscopy Resolves Subcellular Structures in Large Portions of the Songbird Brain |
title_fullStr | Expansion Light Sheet Microscopy Resolves Subcellular Structures in Large Portions of the Songbird Brain |
title_full_unstemmed | Expansion Light Sheet Microscopy Resolves Subcellular Structures in Large Portions of the Songbird Brain |
title_short | Expansion Light Sheet Microscopy Resolves Subcellular Structures in Large Portions of the Songbird Brain |
title_sort | expansion light sheet microscopy resolves subcellular structures in large portions of the songbird brain |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365838/ https://www.ncbi.nlm.nih.gov/pubmed/30766480 http://dx.doi.org/10.3389/fnana.2019.00002 |
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