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HiLo Based Line Scanning Temporal Focusing Microscopy for High-Speed, Deep Tissue Imaging

High-speed, optical-sectioning imaging is highly desired in biomedical studies, as most bio-structures and bio-dynamics are in three-dimensions. Compared to point-scanning techniques, line scanning temporal focusing microscopy (LSTFM) is a promising method that can achieve high temporal resolution w...

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Detalles Bibliográficos
Autores principales: Shi, Ruheng, Zhang, Yuanlong, Zhou, Tiankuang, Kong, Lingjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8400873/
https://www.ncbi.nlm.nih.gov/pubmed/34436397
http://dx.doi.org/10.3390/membranes11080634
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author Shi, Ruheng
Zhang, Yuanlong
Zhou, Tiankuang
Kong, Lingjie
author_facet Shi, Ruheng
Zhang, Yuanlong
Zhou, Tiankuang
Kong, Lingjie
author_sort Shi, Ruheng
collection PubMed
description High-speed, optical-sectioning imaging is highly desired in biomedical studies, as most bio-structures and bio-dynamics are in three-dimensions. Compared to point-scanning techniques, line scanning temporal focusing microscopy (LSTFM) is a promising method that can achieve high temporal resolution while maintaining a deep penetration depth. However, the contrast and axial confinement would still be deteriorated in scattering tissue imaging. Here, we propose a HiLo-based LSTFM, utilizing structured illumination to inhibit the fluorescence background and, thus, enhance the image contrast and axial confinement in deep imaging. We demonstrate the superiority of our method by performing volumetric imaging of neurons and dynamical imaging of microglia in mouse brains in vivo.
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spelling pubmed-84008732021-08-29 HiLo Based Line Scanning Temporal Focusing Microscopy for High-Speed, Deep Tissue Imaging Shi, Ruheng Zhang, Yuanlong Zhou, Tiankuang Kong, Lingjie Membranes (Basel) Article High-speed, optical-sectioning imaging is highly desired in biomedical studies, as most bio-structures and bio-dynamics are in three-dimensions. Compared to point-scanning techniques, line scanning temporal focusing microscopy (LSTFM) is a promising method that can achieve high temporal resolution while maintaining a deep penetration depth. However, the contrast and axial confinement would still be deteriorated in scattering tissue imaging. Here, we propose a HiLo-based LSTFM, utilizing structured illumination to inhibit the fluorescence background and, thus, enhance the image contrast and axial confinement in deep imaging. We demonstrate the superiority of our method by performing volumetric imaging of neurons and dynamical imaging of microglia in mouse brains in vivo. MDPI 2021-08-17 /pmc/articles/PMC8400873/ /pubmed/34436397 http://dx.doi.org/10.3390/membranes11080634 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shi, Ruheng
Zhang, Yuanlong
Zhou, Tiankuang
Kong, Lingjie
HiLo Based Line Scanning Temporal Focusing Microscopy for High-Speed, Deep Tissue Imaging
title HiLo Based Line Scanning Temporal Focusing Microscopy for High-Speed, Deep Tissue Imaging
title_full HiLo Based Line Scanning Temporal Focusing Microscopy for High-Speed, Deep Tissue Imaging
title_fullStr HiLo Based Line Scanning Temporal Focusing Microscopy for High-Speed, Deep Tissue Imaging
title_full_unstemmed HiLo Based Line Scanning Temporal Focusing Microscopy for High-Speed, Deep Tissue Imaging
title_short HiLo Based Line Scanning Temporal Focusing Microscopy for High-Speed, Deep Tissue Imaging
title_sort hilo based line scanning temporal focusing microscopy for high-speed, deep tissue imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8400873/
https://www.ncbi.nlm.nih.gov/pubmed/34436397
http://dx.doi.org/10.3390/membranes11080634
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