Shi Ruheng, Zhang Yuanlong, Zhou Tiankuang, Kong Lingjie
State Key Laboratory of Precision Measurement Technology and Instruments, Department of Precision Instrument, Tsinghua University, Beijing 100084, China.
Department of Automation, Tsinghua University, Beijing 100084, China.
Membranes (Basel). 2021 Aug 17;11(8):634. doi: 10.3390/membranes11080634.
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.
在生物医学研究中,由于大多数生物结构和生物动力学都是三维的,因此非常需要高速光学切片成像。与点扫描技术相比,线扫描时间聚焦显微镜(LSTFM)是一种很有前途的方法,它可以在保持较深穿透深度的同时实现高时间分辨率。然而,在散射组织成像中,对比度和轴向限制仍然会变差。在这里,我们提出了一种基于高低频(HiLo)的LSTFM,利用结构化照明来抑制荧光背景,从而在深度成像中提高图像对比度和轴向限制。我们通过对小鼠大脑中的神经元进行体积成像和对小胶质细胞进行动态成像,证明了我们方法的优越性。