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Label-free, multi-scale imaging of ex-vivo mouse brain using spatial light interference microscopy
Brain connectivity spans over broad spatial scales, from nanometers to centimeters. In order to understand the brain at multi-scale, the neural network in wide-field has been visualized in detail by taking advantage of light microscopy. However, the process of staining or addition of fluorescent tag...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5180101/ https://www.ncbi.nlm.nih.gov/pubmed/28009019 http://dx.doi.org/10.1038/srep39667 |
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author | Min, Eunjung Kandel, Mikhail E. Ko, CheMyong J Popescu, Gabriel Jung, Woonggyu Best-Popescu, Catherine |
author_facet | Min, Eunjung Kandel, Mikhail E. Ko, CheMyong J Popescu, Gabriel Jung, Woonggyu Best-Popescu, Catherine |
author_sort | Min, Eunjung |
collection | PubMed |
description | Brain connectivity spans over broad spatial scales, from nanometers to centimeters. In order to understand the brain at multi-scale, the neural network in wide-field has been visualized in detail by taking advantage of light microscopy. However, the process of staining or addition of fluorescent tags is commonly required, and the image contrast is insufficient for delineation of cytoarchitecture. To overcome this barrier, we use spatial light interference microscopy to investigate brain structure with high-resolution, sub-nanometer pathlength sensitivity without the use of exogenous contrast agents. Combining wide-field imaging and a mosaic algorithm developed in-house, we show the detailed architecture of cells and myelin, within coronal olfactory bulb and cortical sections, and from sagittal sections of the hippocampus and cerebellum. Our technique is well suited to identify laminar characteristics of fiber tract orientation within white matter, e.g. the corpus callosum. To further improve the macro-scale contrast of anatomical structures, and to better differentiate axons and dendrites from cell bodies, we mapped the tissue in terms of its scattering property. Based on our results, we anticipate that spatial light interference microscopy can potentially provide multiscale and multicontrast perspectives of gross and microscopic brain anatomy. |
format | Online Article Text |
id | pubmed-5180101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51801012016-12-29 Label-free, multi-scale imaging of ex-vivo mouse brain using spatial light interference microscopy Min, Eunjung Kandel, Mikhail E. Ko, CheMyong J Popescu, Gabriel Jung, Woonggyu Best-Popescu, Catherine Sci Rep Article Brain connectivity spans over broad spatial scales, from nanometers to centimeters. In order to understand the brain at multi-scale, the neural network in wide-field has been visualized in detail by taking advantage of light microscopy. However, the process of staining or addition of fluorescent tags is commonly required, and the image contrast is insufficient for delineation of cytoarchitecture. To overcome this barrier, we use spatial light interference microscopy to investigate brain structure with high-resolution, sub-nanometer pathlength sensitivity without the use of exogenous contrast agents. Combining wide-field imaging and a mosaic algorithm developed in-house, we show the detailed architecture of cells and myelin, within coronal olfactory bulb and cortical sections, and from sagittal sections of the hippocampus and cerebellum. Our technique is well suited to identify laminar characteristics of fiber tract orientation within white matter, e.g. the corpus callosum. To further improve the macro-scale contrast of anatomical structures, and to better differentiate axons and dendrites from cell bodies, we mapped the tissue in terms of its scattering property. Based on our results, we anticipate that spatial light interference microscopy can potentially provide multiscale and multicontrast perspectives of gross and microscopic brain anatomy. Nature Publishing Group 2016-12-23 /pmc/articles/PMC5180101/ /pubmed/28009019 http://dx.doi.org/10.1038/srep39667 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Min, Eunjung Kandel, Mikhail E. Ko, CheMyong J Popescu, Gabriel Jung, Woonggyu Best-Popescu, Catherine Label-free, multi-scale imaging of ex-vivo mouse brain using spatial light interference microscopy |
title | Label-free, multi-scale imaging of ex-vivo mouse brain using spatial light interference microscopy |
title_full | Label-free, multi-scale imaging of ex-vivo mouse brain using spatial light interference microscopy |
title_fullStr | Label-free, multi-scale imaging of ex-vivo mouse brain using spatial light interference microscopy |
title_full_unstemmed | Label-free, multi-scale imaging of ex-vivo mouse brain using spatial light interference microscopy |
title_short | Label-free, multi-scale imaging of ex-vivo mouse brain using spatial light interference microscopy |
title_sort | label-free, multi-scale imaging of ex-vivo mouse brain using spatial light interference microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5180101/ https://www.ncbi.nlm.nih.gov/pubmed/28009019 http://dx.doi.org/10.1038/srep39667 |
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