| Literature DB >> 29296503 |
Qi Zhang1,2, Xiong Yang1,2, Qinglei Hu1,2, Ke Bai1,2, Fangfang Yin1,2, Ning Li1,2, Yadong Gang1,2, Xiaojun Wang1,2, Shaoqun Zeng1,2.
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.Keywords: (170.0180) Microscopy; (170.2520) Fluorescence microscopy; (170.3880) Medical and biological imaging; (180.6900) Three-dimensional microscopy
Year: 2017 PMID: 29296503 PMCID: PMC5745118 DOI: 10.1364/BOE.8.005767
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732