Advances in Deep-Tissue Light-Sheet Fluorescence Microscopic Imaging (Invited)

被引:1
|
作者
Zhou Xiao [1 ,2 ,3 ]
Zuo Chao [1 ,2 ,3 ]
Liu Yongtao [1 ,2 ,3 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Elect & Opt Engn, Smart Computat Imaging Lab SCILab, Nanjing 210094, Jiangsu, Peoples R China
[2] Nanjing Univ Sci & Technol, Jiangsu Key Lab Spectral Imaging & Intelligent Se, Nanjing 210094, Jiangsu, Peoples R China
[3] Nanjing Univ Sci & Technol, Smart Computat Imaging Res Inst SCIRI, Nanjing 210019, Jiangsu, Peoples R China
关键词
fluorescence microscopy; light-sheet illumination; deep tissue imaging; three-dimensional imaging; optical scattering; PLANE ILLUMINATION MICROSCOPY; ADAPTIVE OPTICS; 2-PHOTON MICROSCOPY; BRAIN; NANOPARTICLES; ZEBRAFISH; EMBRYOS; CANCER; CELLS; DYE;
D O I
10.3788/LOP232599
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
As biomedical research delves deeper into the intricacies of tissue structure and function, the demand for high-resolution, high-signal-to-noise-ratio deep-tissue imaging technologies has become critical. Traditional microscopy, limited to two-dimensional, transparent thin biological samples, falls short in satisfying the current requirements for three-dimensional deep-tissue imaging in biomedical sciences. In contrast, light-sheet fluorescence microscopy distinguishes itself through its attributes-low photodamage, rapid acquisition, extensive field of view, and volumetric imaging-establishing it as a cornerstone among biologists. Despite these advantages, the intrinsic high-scattering characteristics of biological tissues pose formidable challenges to achieving deep imaging. This review focuses on recent progress in light-sheet fluorescence microscopy for deep tissue imaging, emphasizing strategies that overcome challenges associated with high-scattering samples, so as to provide valuable insights to researchers in related fields, assisting them in developing a preliminary comprehension of the latest innovations and future possibilities inherent in this cutting-edge technology. Firstly, the basic principles of light-sheet fluorescence microscopy and the causes and effects of high-scattering absorption characteristics are explained. Subsequently, recent progress in enhancing tissue penetration depth and addressing issues such as light scattering and absorption is further examined. Finally, the development prospects and potential applications of light-sheet fluorescence microscopy imaging technology with high penetration depth and anti-scattering ability are discussed.
引用
收藏
页数:16
相关论文
共 96 条
  • [1] Ahrens MB, 2013, NAT METHODS, V10, P413, DOI [10.1038/NMETH.2434, 10.1038/nmeth.2434]
  • [2] Organic dye doped nanoparticles with NIR emission and biocompatibility for ultra-deep in vivo two-photon microscopy under 1040 nm femtosecond excitation
    Alifu, Nuernisha
    Yan, Lulin
    Zhang, Hequn
    Zebibula, Abudureheman
    Zhu, Zhenggang
    Xi, Wang
    Roe, Anna Wang
    Xu, Bin
    Tian, Wenjing
    Qian, Jun
    [J]. DYES AND PIGMENTS, 2017, 143 : 76 - 85
  • [3] Towards comprehensive cell lineage reconstructions in complex organisms using light-sheet microscopy
    Amat, Fernando
    Keller, Philipp J.
    [J]. DEVELOPMENT GROWTH & DIFFERENTIATION, 2013, 55 (04) : 563 - 578
  • [4] Antaris AL, 2016, NAT MATER, V15, P235, DOI [10.1038/NMAT4476, 10.1038/nmat4476]
  • [5] Seeing through Musculoskeletal Tissues: Improving In Situ Imaging of Bone and the Lacunar Canalicular System through Optical Clearing
    Berke, Ian M.
    Miola, Joseph P.
    David, Michael A.
    Smith, Melanie K.
    Price, Christopher
    [J]. PLOS ONE, 2016, 11 (03):
  • [6] Adaptive optics in microscopy
    Booth, Martin J.
    [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES, 2007, 365 (1861): : 2829 - 2843
  • [7] A tunable refractive index matching medium for live imaging cells, tissues and model organisms
    Boothe, Tobias
    Hilbert, Lennart
    Heide, Michael
    Berninger, Lea
    Huttner, Wieland B.
    Zaburdaev, Vasily
    Vastenhouw, Nadine L.
    Myers, Eugene W.
    Drechsel, David N.
    Rink, Jochen C.
    [J]. ELIFE, 2017, 6
  • [8] 3D adaptive optics in a light sheet microscope
    Bourgenot, Cyril
    Saunter, Christopher D.
    Taylor, Jonathan M.
    Girkin, John M.
    Love, Gordon D.
    [J]. OPTICS EXPRESS, 2012, 20 (12): : 13252 - 13261
  • [9] Microscopic Imaging and Spectroscopy with Scattered Light
    Boustany, Nada N.
    Boppart, Stephen A.
    Backman, Vadim
    [J]. ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, VOL 12, 2010, 12 : 285 - 314
  • [10] 3-DIMENSIONAL CHROMATIN DISTRIBUTION IN NEURO-BLASTOMA NUCLEI SHOWN BY CONFOCAL SCANNING LASER MICROSCOPY
    BRAKENHOFF, GJ
    VANDERVOORT, HTM
    VANSPRONSEN, EA
    LINNEMANS, WAM
    NANNINGA, N
    [J]. NATURE, 1985, 317 (6039) : 748 - 749