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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-8568963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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