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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Main Authors: Ruheng Shi, Yuanlong Zhang, Tiankuang Zhou, Lingjie Kong
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Membranes
Subjects:
Online Access:https://www.mdpi.com/2077-0375/11/8/634
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spelling doaj-957fe4f072d54e73802024f2a4ede5f62021-08-26T14:03:33ZengMDPI AGMembranes2077-03752021-08-011163463410.3390/membranes11080634HiLo Based Line Scanning Temporal Focusing Microscopy for High-Speed, Deep Tissue ImagingRuheng Shi0Yuanlong Zhang1Tiankuang Zhou2Lingjie Kong3State Key Laboratory of Precision Measurement Technology and Instruments, Department of Precision Instrument, Tsinghua University, Beijing 100084, ChinaDepartment of Automation, Tsinghua University, Beijing 100084, ChinaDepartment of Automation, Tsinghua University, Beijing 100084, ChinaState Key Laboratory of Precision Measurement Technology and Instruments, Department of Precision Instrument, Tsinghua University, Beijing 100084, ChinaHigh-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.https://www.mdpi.com/2077-0375/11/8/634HiLo microscopyline scanning temporal focusing microscopydeep tissue imagingcontrast enhancementaxial confinement enhancement
collection DOAJ
language English
format Article
sources DOAJ
author Ruheng Shi
Yuanlong Zhang
Tiankuang Zhou
Lingjie Kong
spellingShingle Ruheng Shi
Yuanlong Zhang
Tiankuang Zhou
Lingjie Kong
HiLo Based Line Scanning Temporal Focusing Microscopy for High-Speed, Deep Tissue Imaging
Membranes
HiLo microscopy
line scanning temporal focusing microscopy
deep tissue imaging
contrast enhancement
axial confinement enhancement
author_facet Ruheng Shi
Yuanlong Zhang
Tiankuang Zhou
Lingjie Kong
author_sort Ruheng Shi
title 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_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_sort hilo based line scanning temporal focusing microscopy for high-speed, deep tissue imaging
publisher MDPI AG
series Membranes
issn 2077-0375
publishDate 2021-08-01
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.
topic HiLo microscopy
line scanning temporal focusing microscopy
deep tissue imaging
contrast enhancement
axial confinement enhancement
url https://www.mdpi.com/2077-0375/11/8/634
work_keys_str_mv AT ruhengshi hilobasedlinescanningtemporalfocusingmicroscopyforhighspeeddeeptissueimaging
AT yuanlongzhang hilobasedlinescanningtemporalfocusingmicroscopyforhighspeeddeeptissueimaging
AT tiankuangzhou hilobasedlinescanningtemporalfocusingmicroscopyforhighspeeddeeptissueimaging
AT lingjiekong hilobasedlinescanningtemporalfocusingmicroscopyforhighspeeddeeptissueimaging
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