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Virtual-scanning light-field microscopy for robust snapshot high-resolution volumetric imaging

High-speed three-dimensional (3D) intravital imaging in animals is useful for studying transient subcellular interactions and functions in health and disease. Light-field microscopy (LFM) provides a computational solution for snapshot 3D imaging with low phototoxicity but is restricted by low resolu...

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Autores principales: Lu, Zhi, Liu, Yu, Jin, Manchang, Luo, Xin, Yue, Huanjing, Wang, Zian, Zuo, Siqing, Zeng, Yunmin, Fan, Jiaqi, Pang, Yanwei, Wu, Jiamin, Yang, Jingyu, Dai, Qionghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172145/
https://www.ncbi.nlm.nih.gov/pubmed/37024654
http://dx.doi.org/10.1038/s41592-023-01839-6
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author Lu, Zhi
Liu, Yu
Jin, Manchang
Luo, Xin
Yue, Huanjing
Wang, Zian
Zuo, Siqing
Zeng, Yunmin
Fan, Jiaqi
Pang, Yanwei
Wu, Jiamin
Yang, Jingyu
Dai, Qionghai
author_facet Lu, Zhi
Liu, Yu
Jin, Manchang
Luo, Xin
Yue, Huanjing
Wang, Zian
Zuo, Siqing
Zeng, Yunmin
Fan, Jiaqi
Pang, Yanwei
Wu, Jiamin
Yang, Jingyu
Dai, Qionghai
author_sort Lu, Zhi
collection PubMed
description High-speed three-dimensional (3D) intravital imaging in animals is useful for studying transient subcellular interactions and functions in health and disease. Light-field microscopy (LFM) provides a computational solution for snapshot 3D imaging with low phototoxicity but is restricted by low resolution and reconstruction artifacts induced by optical aberrations, motion and noise. Here, we propose virtual-scanning LFM (VsLFM), a physics-based deep learning framework to increase the resolution of LFM up to the diffraction limit within a snapshot. By constructing a 40 GB high-resolution scanning LFM dataset across different species, we exploit physical priors between phase-correlated angular views to address the frequency aliasing problem. This enables us to bypass hardware scanning and associated motion artifacts. Here, we show that VsLFM achieves ultrafast 3D imaging of diverse processes such as the beating heart in embryonic zebrafish, voltage activity in Drosophila brains and neutrophil migration in the mouse liver at up to 500 volumes per second.
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spelling pubmed-101721452023-05-12 Virtual-scanning light-field microscopy for robust snapshot high-resolution volumetric imaging Lu, Zhi Liu, Yu Jin, Manchang Luo, Xin Yue, Huanjing Wang, Zian Zuo, Siqing Zeng, Yunmin Fan, Jiaqi Pang, Yanwei Wu, Jiamin Yang, Jingyu Dai, Qionghai Nat Methods Article High-speed three-dimensional (3D) intravital imaging in animals is useful for studying transient subcellular interactions and functions in health and disease. Light-field microscopy (LFM) provides a computational solution for snapshot 3D imaging with low phototoxicity but is restricted by low resolution and reconstruction artifacts induced by optical aberrations, motion and noise. Here, we propose virtual-scanning LFM (VsLFM), a physics-based deep learning framework to increase the resolution of LFM up to the diffraction limit within a snapshot. By constructing a 40 GB high-resolution scanning LFM dataset across different species, we exploit physical priors between phase-correlated angular views to address the frequency aliasing problem. This enables us to bypass hardware scanning and associated motion artifacts. Here, we show that VsLFM achieves ultrafast 3D imaging of diverse processes such as the beating heart in embryonic zebrafish, voltage activity in Drosophila brains and neutrophil migration in the mouse liver at up to 500 volumes per second. Nature Publishing Group US 2023-04-06 2023 /pmc/articles/PMC10172145/ /pubmed/37024654 http://dx.doi.org/10.1038/s41592-023-01839-6 Text en © The Author(s) 2023 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
Lu, Zhi
Liu, Yu
Jin, Manchang
Luo, Xin
Yue, Huanjing
Wang, Zian
Zuo, Siqing
Zeng, Yunmin
Fan, Jiaqi
Pang, Yanwei
Wu, Jiamin
Yang, Jingyu
Dai, Qionghai
Virtual-scanning light-field microscopy for robust snapshot high-resolution volumetric imaging
title Virtual-scanning light-field microscopy for robust snapshot high-resolution volumetric imaging
title_full Virtual-scanning light-field microscopy for robust snapshot high-resolution volumetric imaging
title_fullStr Virtual-scanning light-field microscopy for robust snapshot high-resolution volumetric imaging
title_full_unstemmed Virtual-scanning light-field microscopy for robust snapshot high-resolution volumetric imaging
title_short Virtual-scanning light-field microscopy for robust snapshot high-resolution volumetric imaging
title_sort virtual-scanning light-field microscopy for robust snapshot high-resolution volumetric imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172145/
https://www.ncbi.nlm.nih.gov/pubmed/37024654
http://dx.doi.org/10.1038/s41592-023-01839-6
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