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Functional and multiscale 3D structural investigation of brain tissue through correlative in vivo physiology, synchrotron microtomography and volume electron microscopy
Understanding the function of biological tissues requires a coordinated study of physiology and structure, exploring volumes that contain complete functional units at a detail that resolves the relevant features. Here, we introduce an approach to address this challenge: Mouse brain tissue sections c...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132960/ https://www.ncbi.nlm.nih.gov/pubmed/35614048 http://dx.doi.org/10.1038/s41467-022-30199-6 |
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author | Bosch, Carles Ackels, Tobias Pacureanu, Alexandra Zhang, Yuxin Peddie, Christopher J. Berning, Manuel Rzepka, Norman Zdora, Marie-Christine Whiteley, Isabell Storm, Malte Bonnin, Anne Rau, Christoph Margrie, Troy Collinson, Lucy Schaefer, Andreas T. |
author_facet | Bosch, Carles Ackels, Tobias Pacureanu, Alexandra Zhang, Yuxin Peddie, Christopher J. Berning, Manuel Rzepka, Norman Zdora, Marie-Christine Whiteley, Isabell Storm, Malte Bonnin, Anne Rau, Christoph Margrie, Troy Collinson, Lucy Schaefer, Andreas T. |
author_sort | Bosch, Carles |
collection | PubMed |
description | Understanding the function of biological tissues requires a coordinated study of physiology and structure, exploring volumes that contain complete functional units at a detail that resolves the relevant features. Here, we introduce an approach to address this challenge: Mouse brain tissue sections containing a region where function was recorded using in vivo 2-photon calcium imaging were stained, dehydrated, resin-embedded and imaged with synchrotron X-ray computed tomography with propagation-based phase contrast (SXRT). SXRT provided context at subcellular detail, and could be followed by targeted acquisition of multiple volumes using serial block-face electron microscopy (SBEM). In the olfactory bulb, combining SXRT and SBEM enabled disambiguation of in vivo-assigned regions of interest. In the hippocampus, we found that superficial pyramidal neurons in CA1a displayed a larger density of spine apparati than deeper ones. Altogether, this approach can enable a functional and structural investigation of subcellular features in the context of cells and tissues. |
format | Online Article Text |
id | pubmed-9132960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91329602022-05-27 Functional and multiscale 3D structural investigation of brain tissue through correlative in vivo physiology, synchrotron microtomography and volume electron microscopy Bosch, Carles Ackels, Tobias Pacureanu, Alexandra Zhang, Yuxin Peddie, Christopher J. Berning, Manuel Rzepka, Norman Zdora, Marie-Christine Whiteley, Isabell Storm, Malte Bonnin, Anne Rau, Christoph Margrie, Troy Collinson, Lucy Schaefer, Andreas T. Nat Commun Article Understanding the function of biological tissues requires a coordinated study of physiology and structure, exploring volumes that contain complete functional units at a detail that resolves the relevant features. Here, we introduce an approach to address this challenge: Mouse brain tissue sections containing a region where function was recorded using in vivo 2-photon calcium imaging were stained, dehydrated, resin-embedded and imaged with synchrotron X-ray computed tomography with propagation-based phase contrast (SXRT). SXRT provided context at subcellular detail, and could be followed by targeted acquisition of multiple volumes using serial block-face electron microscopy (SBEM). In the olfactory bulb, combining SXRT and SBEM enabled disambiguation of in vivo-assigned regions of interest. In the hippocampus, we found that superficial pyramidal neurons in CA1a displayed a larger density of spine apparati than deeper ones. Altogether, this approach can enable a functional and structural investigation of subcellular features in the context of cells and tissues. Nature Publishing Group UK 2022-05-25 /pmc/articles/PMC9132960/ /pubmed/35614048 http://dx.doi.org/10.1038/s41467-022-30199-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Bosch, Carles Ackels, Tobias Pacureanu, Alexandra Zhang, Yuxin Peddie, Christopher J. Berning, Manuel Rzepka, Norman Zdora, Marie-Christine Whiteley, Isabell Storm, Malte Bonnin, Anne Rau, Christoph Margrie, Troy Collinson, Lucy Schaefer, Andreas T. Functional and multiscale 3D structural investigation of brain tissue through correlative in vivo physiology, synchrotron microtomography and volume electron microscopy |
title | Functional and multiscale 3D structural investigation of brain tissue through correlative in vivo physiology, synchrotron microtomography and volume electron microscopy |
title_full | Functional and multiscale 3D structural investigation of brain tissue through correlative in vivo physiology, synchrotron microtomography and volume electron microscopy |
title_fullStr | Functional and multiscale 3D structural investigation of brain tissue through correlative in vivo physiology, synchrotron microtomography and volume electron microscopy |
title_full_unstemmed | Functional and multiscale 3D structural investigation of brain tissue through correlative in vivo physiology, synchrotron microtomography and volume electron microscopy |
title_short | Functional and multiscale 3D structural investigation of brain tissue through correlative in vivo physiology, synchrotron microtomography and volume electron microscopy |
title_sort | functional and multiscale 3d structural investigation of brain tissue through correlative in vivo physiology, synchrotron microtomography and volume electron microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132960/ https://www.ncbi.nlm.nih.gov/pubmed/35614048 http://dx.doi.org/10.1038/s41467-022-30199-6 |
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