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Embedding and Chemical Reactivation of Green Fluorescent Protein in the Whole Mouse Brain for Optical Micro-Imaging.绿色荧光蛋白在全脑小鼠中的嵌入与化学再激活用于光学显微成像
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Adaptive light-sheet microscopy for long-term, high-resolution imaging in living organisms.自适应光片显微镜用于活体生物的长期、高分辨率成像。
Nat Biotechnol. 2016 Dec;34(12):1267-1278. doi: 10.1038/nbt.3708. Epub 2016 Oct 31.
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Using Stage- and Slit-Scanning to Improve Contrast and Optical Sectioning in Dual-View Inverted Light Sheet Microscopy (diSPIM).利用阶段扫描和狭缝扫描提高双视图倒置光片显微镜(diSPIM)中的对比度和光学切片能力。
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triSPIM: light sheet microscopy with isotropic super-resolution.三平面结构照明显微术:具有各向同性超分辨率的光片显微镜技术
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Light-sheet microscopy imaging of a whole cleared rat brain with Thy1-GFP transgene.利用 Thy1-GFP 转基因对整个清除的大鼠脑进行光片显微镜成像。
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利用倾斜选择性平面照明与机械切片相结合的大体积组织高轴向分辨率成像系统。

High axial resolution imaging system for large volume tissues using combination of inclined selective plane illumination and mechanical sectioning.

作者信息

Zhang Qi, Yang Xiong, Hu Qinglei, Bai Ke, Yin Fangfang, Li Ning, Gang Yadong, Wang Xiaojun, Zeng Shaoqun

机构信息

Collaborative Innovation Center for Biomedical Engineering, Wuhan National Laboratory for Optoelectronics-Huazhong University of Science and Technology, Wuhan, Hubei 430074, China.

Britton Chance Center and MOE Key Laboratory for Biomedical Photonics, School of Engineering Sciences, Huazhong University of Science and Technology, Wuhan, Hubei 430074, China.

出版信息

Biomed Opt Express. 2017 Nov 27;8(12):5767-5775. doi: 10.1364/BOE.8.005767. eCollection 2017 Dec 1.

DOI:10.1364/BOE.8.005767
PMID:29296503
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5745118/
Abstract

To resolve fine structures of biological systems like neurons, it is required to realize microscopic imaging with sufficient spatial resolution in three dimensional systems. With regular optical imaging systems, high lateral resolution is accessible while high axial resolution is hard to achieve in a large volume. We introduce an imaging system for high 3D resolution fluorescence imaging of large volume tissues. Selective plane illumination was adopted to provide high axial resolution. A scientific CMOS working in sub-array mode kept the imaging area in the sample surface, which restrained the adverse effect of aberrations caused by inclined illumination. Plastic embedding and precise mechanical sectioning extended the axial range and eliminated distortion during the whole imaging process. The combination of these techniques enabled 3D high resolution imaging of large tissues. Fluorescent bead imaging showed resolutions of 0.59 μm, 0.47μm, and 0.59 μm in the x, y, and z directions, respectively. Data acquired from the volume sample of brain tissue demonstrated the applicability of this imaging system. Imaging of different depths showed uniform performance where details could be recognized in either the near-soma area or terminal area, and fine structures of neurons could be seen in both the xy and xz sections.

摘要

为了分辨神经元等生物系统的精细结构,需要在三维系统中实现具有足够空间分辨率的显微成像。对于常规光学成像系统,虽然可以获得高横向分辨率,但在大体积样本中很难实现高轴向分辨率。我们介绍一种用于大体积组织的高3D分辨率荧光成像系统。采用选择性平面照明以提供高轴向分辨率。工作在子阵列模式的科学级互补金属氧化物半导体(scientific CMOS)将成像区域保持在样本表面,这抑制了倾斜照明引起的像差的不利影响。塑料包埋和精确的机械切片扩展了轴向范围,并在整个成像过程中消除了畸变。这些技术的结合实现了大组织的3D高分辨率成像。荧光微球成像在x、y和z方向上的分辨率分别为0.59μm、0.47μm和0.59μm。从脑组织体积样本获取的数据证明了该成像系统的适用性。不同深度的成像显示出均匀的性能,在近胞体区域或终末区域都能识别细节,并且在xy和xz切片中都能看到神经元的精细结构。