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A method for ultrafast tissue clearing that preserves fluorescence for multimodal and longitudinal brain imaging

BACKGROUND: Tissue-clearing techniques have recently been developed to make tissues transparent for three-dimensional (3D) imaging at different scales, including single-cell resolution. However, current tissue-clearing workflows have several disadvantages, including complex protocols, time-consuming...

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Autores principales: Shan, Qing-Hong, Qin, Xin-Ya, Zhou, Nan, Huang, Chuan, Wang, Yu, Chen, Peng, Zhou, Jiang-Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966190/
https://www.ncbi.nlm.nih.gov/pubmed/35351101
http://dx.doi.org/10.1186/s12915-022-01275-6
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author Shan, Qing-Hong
Qin, Xin-Ya
Zhou, Nan
Huang, Chuan
Wang, Yu
Chen, Peng
Zhou, Jiang-Ning
author_facet Shan, Qing-Hong
Qin, Xin-Ya
Zhou, Nan
Huang, Chuan
Wang, Yu
Chen, Peng
Zhou, Jiang-Ning
author_sort Shan, Qing-Hong
collection PubMed
description BACKGROUND: Tissue-clearing techniques have recently been developed to make tissues transparent for three-dimensional (3D) imaging at different scales, including single-cell resolution. However, current tissue-clearing workflows have several disadvantages, including complex protocols, time-consuming application, and fluorescence quenching. Additionally, they can be used mainly for clearing larger-volume samples, preventing wide and easy applicability in conventional experimental approaches. In this study, we aimed to develop a versatile, fast, and convenient method for clearing thin and semi-thick samples, which can be used for three-dimensional imaging of experimental or even clinical samples. RESULTS: We developed an alkaline solution (AKS) containing a combination of 2,2′-thiodiethanol (TDE), DMSO, D-sorbitol, and Tris for tissue clearing, as the alkaline environment is suitable for maintaining the fluorescence of most commonly used fluorescence protein GFP and its variants, and tested its clearing effect on samples from mice and human brains. We assessed the clearing speed, the preservation of fluorescence protein and dyes, and the imaging depth and quality. The results showed that AKS treatment rapidly cleared 300-μm-thick brain slices and 1-mm-thick slices from different organs within 5 min and 1 h, respectively. Moreover, AKS was compatible with a variety of fluorescence proteins and dyes. Most importantly, AKS enhanced the fluorescence of YFP, in contrast to the majority of existing tissue-clearing methods which reduce the fluorescence intensity of fluorescent proteins. Using AKS, we performed long-time high-resolution imaging of weak fluorescent protein-labelled tissues, long-distance fibre tracking, larger-scale 3D imaging and cell counting of the entire brain area, neural circuit tracing, 3D neuromorphic reconstruction, and 3D histopathology imaging. CONCLUSIONS: AKS can be used for simple and rapid clearing of samples from mice and human brains and is widely compatible with a variety of fluorescent dyes. Therefore, AKS has great potential to be used as a broad tissue-clearing reagent for biological optical imaging, especially for time-sensitive experiments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01275-6.
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spelling pubmed-89661902022-03-31 A method for ultrafast tissue clearing that preserves fluorescence for multimodal and longitudinal brain imaging Shan, Qing-Hong Qin, Xin-Ya Zhou, Nan Huang, Chuan Wang, Yu Chen, Peng Zhou, Jiang-Ning BMC Biol Methodology Article BACKGROUND: Tissue-clearing techniques have recently been developed to make tissues transparent for three-dimensional (3D) imaging at different scales, including single-cell resolution. However, current tissue-clearing workflows have several disadvantages, including complex protocols, time-consuming application, and fluorescence quenching. Additionally, they can be used mainly for clearing larger-volume samples, preventing wide and easy applicability in conventional experimental approaches. In this study, we aimed to develop a versatile, fast, and convenient method for clearing thin and semi-thick samples, which can be used for three-dimensional imaging of experimental or even clinical samples. RESULTS: We developed an alkaline solution (AKS) containing a combination of 2,2′-thiodiethanol (TDE), DMSO, D-sorbitol, and Tris for tissue clearing, as the alkaline environment is suitable for maintaining the fluorescence of most commonly used fluorescence protein GFP and its variants, and tested its clearing effect on samples from mice and human brains. We assessed the clearing speed, the preservation of fluorescence protein and dyes, and the imaging depth and quality. The results showed that AKS treatment rapidly cleared 300-μm-thick brain slices and 1-mm-thick slices from different organs within 5 min and 1 h, respectively. Moreover, AKS was compatible with a variety of fluorescence proteins and dyes. Most importantly, AKS enhanced the fluorescence of YFP, in contrast to the majority of existing tissue-clearing methods which reduce the fluorescence intensity of fluorescent proteins. Using AKS, we performed long-time high-resolution imaging of weak fluorescent protein-labelled tissues, long-distance fibre tracking, larger-scale 3D imaging and cell counting of the entire brain area, neural circuit tracing, 3D neuromorphic reconstruction, and 3D histopathology imaging. CONCLUSIONS: AKS can be used for simple and rapid clearing of samples from mice and human brains and is widely compatible with a variety of fluorescent dyes. Therefore, AKS has great potential to be used as a broad tissue-clearing reagent for biological optical imaging, especially for time-sensitive experiments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01275-6. BioMed Central 2022-03-29 /pmc/articles/PMC8966190/ /pubmed/35351101 http://dx.doi.org/10.1186/s12915-022-01275-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology Article
Shan, Qing-Hong
Qin, Xin-Ya
Zhou, Nan
Huang, Chuan
Wang, Yu
Chen, Peng
Zhou, Jiang-Ning
A method for ultrafast tissue clearing that preserves fluorescence for multimodal and longitudinal brain imaging
title A method for ultrafast tissue clearing that preserves fluorescence for multimodal and longitudinal brain imaging
title_full A method for ultrafast tissue clearing that preserves fluorescence for multimodal and longitudinal brain imaging
title_fullStr A method for ultrafast tissue clearing that preserves fluorescence for multimodal and longitudinal brain imaging
title_full_unstemmed A method for ultrafast tissue clearing that preserves fluorescence for multimodal and longitudinal brain imaging
title_short A method for ultrafast tissue clearing that preserves fluorescence for multimodal and longitudinal brain imaging
title_sort method for ultrafast tissue clearing that preserves fluorescence for multimodal and longitudinal brain imaging
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966190/
https://www.ncbi.nlm.nih.gov/pubmed/35351101
http://dx.doi.org/10.1186/s12915-022-01275-6
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