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Mirror-enhanced scanning light-field microscopy for long-term high-speed 3D imaging with isotropic resolution

Various biological behaviors can only be observed in 3D at high speed over the long term with low phototoxicity. Light-field microscopy (LFM) provides an elegant compact solution to record 3D information in a tomographic manner simultaneously, which can facilitate high photon efficiency. However, LF...

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Autores principales: Xiong, Bo, Zhu, Tianyi, Xiang, Yuhan, Li, Xiaopeng, Yu, Jinqiang, Jiang, Zheng, Niu, Yihan, Jiang, Dong, Zhang, Xu, Fang, Lu, Wu, Jiamin, Dai, Qionghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568963/
https://www.ncbi.nlm.nih.gov/pubmed/34737265
http://dx.doi.org/10.1038/s41377-021-00665-9
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author Xiong, Bo
Zhu, Tianyi
Xiang, Yuhan
Li, Xiaopeng
Yu, Jinqiang
Jiang, Zheng
Niu, Yihan
Jiang, Dong
Zhang, Xu
Fang, Lu
Wu, Jiamin
Dai, Qionghai
author_facet Xiong, Bo
Zhu, Tianyi
Xiang, Yuhan
Li, Xiaopeng
Yu, Jinqiang
Jiang, Zheng
Niu, Yihan
Jiang, Dong
Zhang, Xu
Fang, Lu
Wu, Jiamin
Dai, Qionghai
author_sort Xiong, Bo
collection PubMed
description Various biological behaviors can only be observed in 3D at high speed over the long term with low phototoxicity. Light-field microscopy (LFM) provides an elegant compact solution to record 3D information in a tomographic manner simultaneously, which can facilitate high photon efficiency. However, LFM still suffers from the missing-cone problem, leading to degraded axial resolution and ringing effects after deconvolution. Here, we propose a mirror-enhanced scanning LFM (MiSLFM) to achieve long-term high-speed 3D imaging at super-resolved axial resolution with a single objective, by fully exploiting the extended depth of field of LFM with a tilted mirror placed below samples. To establish the unique capabilities of MiSLFM, we performed extensive experiments, we observed various organelle interactions and intercellular interactions in different types of photosensitive cells under extremely low light conditions. Moreover, we demonstrated that superior axial resolution facilitates more robust blood cell tracking in zebrafish larvae at high speed.
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spelling pubmed-85689632021-11-08 Mirror-enhanced scanning light-field microscopy for long-term high-speed 3D imaging with isotropic resolution Xiong, Bo Zhu, Tianyi Xiang, Yuhan Li, Xiaopeng Yu, Jinqiang Jiang, Zheng Niu, Yihan Jiang, Dong Zhang, Xu Fang, Lu Wu, Jiamin Dai, Qionghai Light Sci Appl Article Various biological behaviors can only be observed in 3D at high speed over the long term with low phototoxicity. Light-field microscopy (LFM) provides an elegant compact solution to record 3D information in a tomographic manner simultaneously, which can facilitate high photon efficiency. However, LFM still suffers from the missing-cone problem, leading to degraded axial resolution and ringing effects after deconvolution. Here, we propose a mirror-enhanced scanning LFM (MiSLFM) to achieve long-term high-speed 3D imaging at super-resolved axial resolution with a single objective, by fully exploiting the extended depth of field of LFM with a tilted mirror placed below samples. To establish the unique capabilities of MiSLFM, we performed extensive experiments, we observed various organelle interactions and intercellular interactions in different types of photosensitive cells under extremely low light conditions. Moreover, we demonstrated that superior axial resolution facilitates more robust blood cell tracking in zebrafish larvae at high speed. Nature Publishing Group UK 2021-11-04 /pmc/articles/PMC8568963/ /pubmed/34737265 http://dx.doi.org/10.1038/s41377-021-00665-9 Text en © The Author(s) 2021 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
Xiong, Bo
Zhu, Tianyi
Xiang, Yuhan
Li, Xiaopeng
Yu, Jinqiang
Jiang, Zheng
Niu, Yihan
Jiang, Dong
Zhang, Xu
Fang, Lu
Wu, Jiamin
Dai, Qionghai
Mirror-enhanced scanning light-field microscopy for long-term high-speed 3D imaging with isotropic resolution
title Mirror-enhanced scanning light-field microscopy for long-term high-speed 3D imaging with isotropic resolution
title_full Mirror-enhanced scanning light-field microscopy for long-term high-speed 3D imaging with isotropic resolution
title_fullStr Mirror-enhanced scanning light-field microscopy for long-term high-speed 3D imaging with isotropic resolution
title_full_unstemmed Mirror-enhanced scanning light-field microscopy for long-term high-speed 3D imaging with isotropic resolution
title_short Mirror-enhanced scanning light-field microscopy for long-term high-speed 3D imaging with isotropic resolution
title_sort mirror-enhanced scanning light-field microscopy for long-term high-speed 3d imaging with isotropic resolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568963/
https://www.ncbi.nlm.nih.gov/pubmed/34737265
http://dx.doi.org/10.1038/s41377-021-00665-9
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