Chinese Optics, Volume. 15, Issue 6, 1321(2022)

Double-ring-modulated light sheet fluorescence microscopic technique for multi-scale high-resolution 3D imaging

Peng WANG1, Yao ZHOU1, Yu-xuan ZHAO1, and Peng FEI1,2、*
Author Affiliations
  • 1School of Optical and Electronic Information, Huazhong University of Science and Technology, Wuhan 430074, China
  • 2Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan 430074, China
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    References(33)

    [1] LICHTMAN J W, CONCHELLO J A. Fluorescence microscopy[J]. Nature Methods, 2, 910-919(2005).

    [2] CHOQUET D, SAINLOS M, SIBARITA J B. Advanced imaging and labelling methods to decipher brain cell organization and function[J]. Nature Reviews Neuroscience, 22, 237-255(2021).

    [3] STELZER E H K, STROBL F, CHANG B J, et al. Light sheet fluorescence microscopy[J]. Nature Reviews Methods Primers, 1, 73(2021).

    [4] HUISKEN J, SWOGER J, DEL BENE F, et al. Optical sectioning deep inside live embryos by selective plane illumination microscopy[J]. Science, 305, 1007-1009(2004).

    [5] KELLER P J, SCHMIDT A D, WITTBRODT J, et al. Reconstruction of zebrafish early embryonic development by scanned light sheet microscopy[J]. Science, 322, 1065-1069(2008).

    [6] DEAN K M, ROUDOT P, WELF E S, et al. Deconvolution-free subcellular imaging with axially swept light sheet microscopy[J]. Biophysical Journal, 108, 2807-2815(2015).

    [7] FAHRBACH F O, GURCHENKOV V, ALESSANDRI K, et al. Self-reconstructing sectioned Bessel beams offer submicron optical sectioning for large fields of view in light-sheet microscopy[J]. Optics Express, 21, 11425-11440(2013).

    [8] LIU Y CH, KE Y G, ZHOU J X, et al. Generation of perfect vortex and vector beams based on Pancharatnam-Berry phase elements[J]. Scientific Reports, 7, 44096(2017).

    [9] ZHAO T, LAU S C, WANG Y, et al. Multicolor 4D fluorescence microscopy using ultrathin bessel light sheets[J]. Scientific Reports, 6, 26159(2016).

    [10] CAO B, COELHO S, LI J R, et al. Volumetric interferometric lattice light-sheet imaging[J]. Nature Biotechnology, 39, 1385-1393(2021).

    [11] CHANG B J, KITTISOPIKUL M, DEAN K M, et al. Universal light-sheet generation with field synthesis[J]. Nature Methods, 16, 235-238(2019).

    [12] DUNSBY C. Optically sectioned imaging by oblique plane microscopy[J]. Optics Express, 16, 20306-20316(2008).

    [13] YANG B, LANGE M, MILLETT-SIKKING A, et al. DaXi—high-resolution, large imaging volume and multi-view single-objective light-sheet microscopy[J]. Nature Methods, 19, 461-469(2022).

    [14] POWER R M, HUISKEN J. A guide to light-sheet fluorescence microscopy for multiscale imaging[J]. Nature Methods, 14, 360-373(2017).

    [15] MORI S. Side lobe suppression of a Bessel beam for high aspect ratio laser processing[J]. Precision Engineering, 39, 79-85(2015).

    [16] [16] YU D Y, TAN H Y. Engineering Optics[M]. Beijing: China Machine Press, 2015. (in Chinese)

    [17] ZHAO Y X, ZHANG M, ZHANG W T, et al. Isotropic super-resolution light-sheet microscopy of dynamic intracellular structures at subsecond timescales[J]. Nature Methods, 19, 359-369(2022).

    [18] SCHERMELLEH L, FERRAND A, HUSER T, et al. Super-resolution microscopy demystified[J]. Nature Cell Biology, 21, 72-84(2019).

    [19] WU Y C, HAN X F, SU Y J, et al. Multiview confocal super-resolution microscopy[J]. Nature, 600, 279-284(2021).

    [20] VALLI J, GARCIA-BURGOS A, ROONEY L M, et al. Seeing beyond the limit: a guide to choosing the right super-resolution microscopy technique[J]. Journal of Biological Chemistry, 297, 100791(2021).

    [21] ZHAO W S, ZHAO SH Q, LI L J, et al. Sparse deconvolution improves the resolution of live-cell super-resolution fluorescence microscopy[J]. Nature Biotechnology, 40, 606-617(2022).

    [22] HUANG X SH, FAN J CH, LI L J, et al. Fast, long-term, super-resolution imaging with Hessian structured illumination microscopy[J]. Nature Biotechnology, 36, 451-459(2018).

    [23] QIAO CH, LI D, GUO Y T, et al. Evaluation and development of deep neural networks for image super-resolution in optical microscopy[J]. Nature Methods, 18, 194-202(2021).

    [24] ZHELUDEV N I, YUAN G H. Optical superoscillation technologies beyond the diffraction limit[J]. Nature Reviews Physics, 4, 16-32(2022).

    [25] BODÉN A, PENNACCHIETTI F, COCEANO G, et al. Volumetric live cell imaging with three-dimensional parallelized RESOLFT microscopy[J]. Nature Biotechnology, 39, 609-618(2021).

    [26] SUN D E, FAN X Q, SHI Y J, et al. Click-ExM enables expansion microscopy for all biomolecules[J]. Nature Methods, 18, 107-113(2021).

    [27] GAO R X, YU C C, GAO L Y, et al. A highly homogeneous polymer composed of tetrahedron-like monomers for high-isotropy expansion microscopy[J]. Nature Nanotechnology, 16, 698-707(2021).

    [28] THEVATHASAN J V, KAHNWALD M, CIEŚLIŃSKI K, et al. Nuclear pores as versatile reference standards for quantitative superresolution microscopy[J]. Nature Methods, 16, 1045-1053(2019).

    [29] JING D, ZHANG SH W, LUO W J, et al. Tissue clearing of both hard and soft tissue organs with the pegasos method[J]. Cell Research, 28, 803-818(2018).

    [30] ZHU J T, LIU X M, DENG Y T, et al. Tissue optical clearing for 3D visualization of vascular networks: a review[J]. Vascular Pharmacology, 141, 106905(2021).

    [31] SUN Q T, LI X N, REN M, et al. A whole-brain map of long-range inputs to GABAergic interneurons in the mouse medial prefrontal cortex[J]. Nature Neuroscience, 22, 1357-1370(2019).

    [32] FANG CH Y, YU T T, CHU T T, et al. Minutes-timescale 3D isotropic imaging of entire organs at subcellular resolution by content-aware compressed-sensing light-sheet microscopy[J]. Nature Communications, 12, 107(2021).

    [33] XU F, SHEN Y, DING L F, et al. High-throughput mapping of a whole rhesus monkey brain at micrometer resolution[J]. Nature Biotechnology, 39, 1521-1528(2021).

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    Peng WANG, Yao ZHOU, Yu-xuan ZHAO, Peng FEI. Double-ring-modulated light sheet fluorescence microscopic technique for multi-scale high-resolution 3D imaging[J]. Chinese Optics, 2022, 15(6): 1321

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    Paper Information

    Category: Original Article

    Received: May. 9, 2022

    Accepted: Jul. 7, 2022

    Published Online: Feb. 9, 2023

    The Author Email:

    DOI:10.37188/CO.2022-0093

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