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

被引:2
|
作者
Shi, Ruheng [1 ]
Zhang, Yuanlong [2 ]
Zhou, Tiankuang [2 ,3 ]
Kong, Lingjie [1 ,4 ]
机构
[1] Tsinghua Univ, Dept Precis Instrument, State Key Lab Precis Measurement Technol & Instru, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Dept Automat, Beijing 100084, Peoples R China
[3] Tsinghua Univ, Grad Sch Shenzhen, Shenzhen 518055, Peoples R China
[4] Tsinghua Univ, IDG McGovern Inst Brain Res, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
HiLo microscopy; line scanning temporal focusing microscopy; deep tissue imaging; contrast enhancement; axial confinement enhancement; STRUCTURED ILLUMINATION MICROSCOPY; ADAPTIVE OPTICS; 2-PHOTON; SCATTERING; RESOLUTION;
D O I
10.3390/membranes11080634
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页数:9
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