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Single-scan volumetric imaging throughout thick tissue specimens by one-touch installable light-needle creating device

Biological tissues and their networks frequently change dynamically across large volumes. Understanding network operations requires monitoring their activities in three dimensions (3D) with single-cell resolution. Several researchers have proposed various volumetric imaging technologies. However, mo...

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Autores principales: Chang, Ching-Pu, Otomo, Kohei, Kozawa, Yuichi, Ishii, Hirokazu, Yamasaki, Miwako, Watanabe, Masahiko, Sato, Shunichi, Enoki, Ryosuke, Nemoto, Tomomi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213396/
https://www.ncbi.nlm.nih.gov/pubmed/35729283
http://dx.doi.org/10.1038/s41598-022-14647-3
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author Chang, Ching-Pu
Otomo, Kohei
Kozawa, Yuichi
Ishii, Hirokazu
Yamasaki, Miwako
Watanabe, Masahiko
Sato, Shunichi
Enoki, Ryosuke
Nemoto, Tomomi
author_facet Chang, Ching-Pu
Otomo, Kohei
Kozawa, Yuichi
Ishii, Hirokazu
Yamasaki, Miwako
Watanabe, Masahiko
Sato, Shunichi
Enoki, Ryosuke
Nemoto, Tomomi
author_sort Chang, Ching-Pu
collection PubMed
description Biological tissues and their networks frequently change dynamically across large volumes. Understanding network operations requires monitoring their activities in three dimensions (3D) with single-cell resolution. Several researchers have proposed various volumetric imaging technologies. However, most technologies require large-scale and complicated optical setups, as well as deep expertise for microscopic technologies, resulting in a high threshold for biologists. In this study, we propose an easy-to-use light-needle creating device for conventional two-photon microscopy systems. By only installing the device in one position for a filter cube that conventional fluorescent microscopes have, single scanning of the excitation laser light beam excited fluorophores throughout over 200 μm thickness specimens simultaneously. Furthermore, the developed microscopy system successfully demonstrated single-scan visualization of the 3D structure of transparent YFP-expressing brain slices. Finally, in acute mouse cortical slices with a thickness of approximately 250 μm, we detected calcium activities with 7.5 Hz temporal resolution in the neuronal population.
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spelling pubmed-92133962022-06-23 Single-scan volumetric imaging throughout thick tissue specimens by one-touch installable light-needle creating device Chang, Ching-Pu Otomo, Kohei Kozawa, Yuichi Ishii, Hirokazu Yamasaki, Miwako Watanabe, Masahiko Sato, Shunichi Enoki, Ryosuke Nemoto, Tomomi Sci Rep Article Biological tissues and their networks frequently change dynamically across large volumes. Understanding network operations requires monitoring their activities in three dimensions (3D) with single-cell resolution. Several researchers have proposed various volumetric imaging technologies. However, most technologies require large-scale and complicated optical setups, as well as deep expertise for microscopic technologies, resulting in a high threshold for biologists. In this study, we propose an easy-to-use light-needle creating device for conventional two-photon microscopy systems. By only installing the device in one position for a filter cube that conventional fluorescent microscopes have, single scanning of the excitation laser light beam excited fluorophores throughout over 200 μm thickness specimens simultaneously. Furthermore, the developed microscopy system successfully demonstrated single-scan visualization of the 3D structure of transparent YFP-expressing brain slices. Finally, in acute mouse cortical slices with a thickness of approximately 250 μm, we detected calcium activities with 7.5 Hz temporal resolution in the neuronal population. Nature Publishing Group UK 2022-06-21 /pmc/articles/PMC9213396/ /pubmed/35729283 http://dx.doi.org/10.1038/s41598-022-14647-3 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chang, Ching-Pu
Otomo, Kohei
Kozawa, Yuichi
Ishii, Hirokazu
Yamasaki, Miwako
Watanabe, Masahiko
Sato, Shunichi
Enoki, Ryosuke
Nemoto, Tomomi
Single-scan volumetric imaging throughout thick tissue specimens by one-touch installable light-needle creating device
title Single-scan volumetric imaging throughout thick tissue specimens by one-touch installable light-needle creating device
title_full Single-scan volumetric imaging throughout thick tissue specimens by one-touch installable light-needle creating device
title_fullStr Single-scan volumetric imaging throughout thick tissue specimens by one-touch installable light-needle creating device
title_full_unstemmed Single-scan volumetric imaging throughout thick tissue specimens by one-touch installable light-needle creating device
title_short Single-scan volumetric imaging throughout thick tissue specimens by one-touch installable light-needle creating device
title_sort single-scan volumetric imaging throughout thick tissue specimens by one-touch installable light-needle creating device
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213396/
https://www.ncbi.nlm.nih.gov/pubmed/35729283
http://dx.doi.org/10.1038/s41598-022-14647-3
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