Multifocus microscopy with optical sectioning and high axial resolution

被引:7
|
作者
Strohl, Florian [1 ]
Hansen, Daniel Henry [1 ]
Grifo, Mireia Nager [2 ]
Birgisdottir, Asa Birna [2 ,3 ]
机构
[1] UiT Arctic Univ Norway, Dept Phys & Technol, Tromso, Norway
[2] Univ Hosp North Norway, Div Cardiothorac & Resp Med, Tromso, Norway
[3] UiT Arctic Univ Norway, Dept Clin Med, Tromso, Norway
来源
OPTICA | 2022年 / 9卷 / 11期
基金
欧盟地平线“2020”;
关键词
FLUORESCENCE MICROSCOPY; 3D; LIVE;
D O I
10.1364/OPTICA.468583
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Multifocus microscopy enables recording of entire volumes in a single camera exposure. In dense samples, multifocus microscopy is severely hampered by background haze. Here, we introduce a scalable multifocus method that incorporates optical sectioning and offers improved axial resolution capabilities. In our method, a dithered oblique light-sheet scans the sample volume during a single exposure, while fluorescence from each illuminated plane in the sample is mapped onto a line on the camera with a multifocus optical element. A synchronized rolling shutter readout realizes optical sectioning. We describe the technique theoretically and verify its optical sectioning and resolution improvement capabilities. We demonstrate a prototype system with a multifocus beam splitter cascade and record monolayers of endothelial cells at 35 volumes per second. We furthermore image uncleared engineered human heart tissue and visualize the distribution of mitochondria at high axial resolution. Our method manages to capture sub-diffraction sized mitochondria-derived vesicles up to 30 mu m deep into the tissue.(c) 2022 Optica Publishing Group under the terms of the Optica Open Access Publishing Agreement
引用
收藏
页码:1210 / 1218
页数:9
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