Literature DB >> 33996232

Open-top axially swept light-sheet microscopy.

Bumju Kim1, Myeongsu Na2, Soohyun Park3, Kitae Kim2, Jung-Hoon Park4, Euiheon Chung5, Sunghoe Chang2, Ki Hean Kim1,3.   

Abstract

Open-top light-sheet microscopy (OT-LSM) is a specialized microscopic technique for high throughput cellular imaging of large tissue specimens including optically cleared tissues by having the entire optical setup below the sample stage. Current OT-LSM systems had relatively low axial resolutions by using weakly focused light sheets to cover the imaging field of view (FOV). In this report, open-top axially swept LSM (OTAS-LSM) was developed for high-throughput cellular imaging with improved axial resolution. OTAS-LSM swept a tightly focused excitation light sheet across the imaging FOV using an electro tunable lens (ETL) and collected emission light at the focus of the light sheet with a camera in the rolling shutter mode. OTAS-LSM was developed by using air objective lenses and a liquid prism and it had on-axis optical aberration associated with the mismatch of refractive indices between air and immersion medium. The effects of optical aberration were analyzed by both simulation and experiment, and the image resolutions were under 1.6µm in all directions. The newly developed OTAS-LSM was applied to the imaging of optically cleared mouse brain and small intestine, and it demonstrated the single-cell resolution imaging of neuronal networks. OTAS-LSM might be useful for the high-throughput cellular examination of optically cleared large tissues.
© 2021 Optical Society of America under the terms of the OSA Open Access Publishing Agreement.

Entities:  

Year:  2021        PMID: 33996232      PMCID: PMC8086456          DOI: 10.1364/BOE.419030

Source DB:  PubMed          Journal:  Biomed Opt Express        ISSN: 2156-7085            Impact factor:   3.732


  3 in total

Review 1.  Practical considerations for quantitative light sheet fluorescence microscopy.

Authors:  Chad M Hobson; Min Guo; Harshad D Vishwasrao; Yicong Wu; Hari Shroff; Teng-Leong Chew
Journal:  Nat Methods       Date:  2022-10-20       Impact factor: 47.990

2.  Deep learning enables reference-free isotropic super-resolution for volumetric fluorescence microscopy.

Authors:  Hyoungjun Park; Myeongsu Na; Bumju Kim; Soohyun Park; Ki Hean Kim; Sunghoe Chang; Jong Chul Ye
Journal:  Nat Commun       Date:  2022-06-08       Impact factor: 17.694

3.  DaXi-high-resolution, large imaging volume and multi-view single-objective light-sheet microscopy.

Authors:  Bin Yang; Merlin Lange; Alfred Millett-Sikking; Xiang Zhao; Jordão Bragantini; Shruthi VijayKumar; Mason Kamb; Rafael Gómez-Sjöberg; Ahmet Can Solak; Wanpeng Wang; Hirofumi Kobayashi; Matthew N McCarroll; Lachlan W Whitehead; Reto P Fiolka; Thomas B Kornberg; Andrew G York; Loic A Royer
Journal:  Nat Methods       Date:  2022-03-21       Impact factor: 28.547

  3 in total

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