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Improved clearing method contributes to deep imaging of plant organs
Tissue clearing methods are increasingly essential for the microscopic observation of internal tissues of thick biological organs. We previously developed TOMEI, a clearing method for plant tissues; however, it could not entirely remove chlorophylls nor reduce the fluorescent signal of fluorescent p...
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/PMC8748589/ https://www.ncbi.nlm.nih.gov/pubmed/35013509 http://dx.doi.org/10.1038/s42003-021-02955-9 |
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author | Sakamoto, Yuki Ishimoto, Anna Sakai, Yuuki Sato, Moeko Nishihama, Ryuichi Abe, Konami Sano, Yoshitake Furuichi, Teiichi Tsuji, Hiroyuki Kohchi, Takayuki Matsunaga, Sachihiro |
author_facet | Sakamoto, Yuki Ishimoto, Anna Sakai, Yuuki Sato, Moeko Nishihama, Ryuichi Abe, Konami Sano, Yoshitake Furuichi, Teiichi Tsuji, Hiroyuki Kohchi, Takayuki Matsunaga, Sachihiro |
author_sort | Sakamoto, Yuki |
collection | PubMed |
description | Tissue clearing methods are increasingly essential for the microscopic observation of internal tissues of thick biological organs. We previously developed TOMEI, a clearing method for plant tissues; however, it could not entirely remove chlorophylls nor reduce the fluorescent signal of fluorescent proteins. Here, we developed an improved TOMEI method (iTOMEI) to overcome these limitations. First, a caprylyl sulfobetaine was determined to efficiently remove chlorophylls from Arabidopsis thaliana seedlings without GFP quenching. Next, a weak alkaline solution restored GFP fluorescence, which was mainly lost during fixation, and an iohexol solution with a high refractive index increased sample transparency. These procedures were integrated to form iTOMEI. iTOMEI enables the detection of much brighter fluorescence than previous methods in tissues of A. thaliana, Oryza sativa, and Marchantia polymorpha. Moreover, a mouse brain was also efficiently cleared by the iTOMEI-Brain method within 48 h, and strong fluorescent signals were detected in the cleared brain. |
format | Online Article Text |
id | pubmed-8748589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87485892022-01-20 Improved clearing method contributes to deep imaging of plant organs Sakamoto, Yuki Ishimoto, Anna Sakai, Yuuki Sato, Moeko Nishihama, Ryuichi Abe, Konami Sano, Yoshitake Furuichi, Teiichi Tsuji, Hiroyuki Kohchi, Takayuki Matsunaga, Sachihiro Commun Biol Article Tissue clearing methods are increasingly essential for the microscopic observation of internal tissues of thick biological organs. We previously developed TOMEI, a clearing method for plant tissues; however, it could not entirely remove chlorophylls nor reduce the fluorescent signal of fluorescent proteins. Here, we developed an improved TOMEI method (iTOMEI) to overcome these limitations. First, a caprylyl sulfobetaine was determined to efficiently remove chlorophylls from Arabidopsis thaliana seedlings without GFP quenching. Next, a weak alkaline solution restored GFP fluorescence, which was mainly lost during fixation, and an iohexol solution with a high refractive index increased sample transparency. These procedures were integrated to form iTOMEI. iTOMEI enables the detection of much brighter fluorescence than previous methods in tissues of A. thaliana, Oryza sativa, and Marchantia polymorpha. Moreover, a mouse brain was also efficiently cleared by the iTOMEI-Brain method within 48 h, and strong fluorescent signals were detected in the cleared brain. Nature Publishing Group UK 2022-01-10 /pmc/articles/PMC8748589/ /pubmed/35013509 http://dx.doi.org/10.1038/s42003-021-02955-9 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 Sakamoto, Yuki Ishimoto, Anna Sakai, Yuuki Sato, Moeko Nishihama, Ryuichi Abe, Konami Sano, Yoshitake Furuichi, Teiichi Tsuji, Hiroyuki Kohchi, Takayuki Matsunaga, Sachihiro Improved clearing method contributes to deep imaging of plant organs |
title | Improved clearing method contributes to deep imaging of plant organs |
title_full | Improved clearing method contributes to deep imaging of plant organs |
title_fullStr | Improved clearing method contributes to deep imaging of plant organs |
title_full_unstemmed | Improved clearing method contributes to deep imaging of plant organs |
title_short | Improved clearing method contributes to deep imaging of plant organs |
title_sort | improved clearing method contributes to deep imaging of plant organs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748589/ https://www.ncbi.nlm.nih.gov/pubmed/35013509 http://dx.doi.org/10.1038/s42003-021-02955-9 |
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