Live-cell microscopy - tips and tools

被引:206
|
作者
Frigault, Melanie M. [2 ]
Lacoste, Judith [1 ,3 ]
Swift, Jody L. [4 ]
Brown, Claire M. [1 ]
机构
[1] McGill Univ, Dept Biochem, Life Sci Complex Imaging Facil, Montreal, PQ, Canada
[2] McGill Univ, Ctr Canc, Mol Oncol Grp, Montreal, PQ H3G 1Y6, Canada
[3] McGill Univ, Dept Biol, Cell Imaging & Anal Network, Montreal, PQ H3G 1Y6, Canada
[4] McGill Univ, Dept Chem, Montreal, PQ H3G 1Y6, Canada
关键词
CLSM; Multi-photon; TIRF; Live-cell imaging; Spinning disk; REFLECTION FLUORESCENCE MICROSCOPY; IMAGE CORRELATION SPECTROSCOPY; RESONANCE ENERGY-TRANSFER; LIVING CELLS; 2-PHOTON EXCITATION; REGULATES ADHESION; PRACTICAL ASPECTS; PROTEIN DYNAMICS; GUIDE; DECONVOLUTION;
D O I
10.1242/jcs.033837
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Imaging of living cells and tissue is now common in many fields of the life and physical sciences, and is instrumental in revealing a great deal about cellular dynamics and function. It is crucial when performing such experiments that cell viability is at the forefront of any measurement to ensure that the physiological and biological processes that are under investigation are not altered in any way. Many cells and tissues are not normally exposed to light during their life cycle, so it is important for microscopy applications to minimize light exposure, which can cause phototoxicity. To ensure minimal light exposure, it is crucial that microscope systems are optimized to collect as much light as possible. This can be achieved using superior-quality optical components and state-of-the-art detectors. This Commentary discusses how to set up a suitable environment on the microscope stage to maintain living cells. There is also a focus on general and imaging-platform-specific ways to optimize the efficiency of light throughput and detection. With an efficient optical microscope and a good detector, the light exposure can be minimized during live-cell imaging, thus minimizing phototoxicity and maintaining cell viability. Brief suggestions for useful microscope accessories as well as available fluorescence tools are also presented. Finally, a flow chart is provided to assist readers in choosing the appropriate imaging platform for their experimental systems.
引用
下载
收藏
页码:753 / 767
页数:15
相关论文
共 50 条
  • [21] Live-cell microscopy: Environmental control for mammalian specimens
    Focht, DC
    NATURE BIOTECHNOLOGY, 1996, 14 (03) : 361 - 362
  • [22] Live-Cell Super-resolution Fluorescence Microscopy
    A. S. Mishin
    K. A. Lukyanov
    Biochemistry (Moscow), 2019, 84 : 19 - 31
  • [23] A Critical and Comparative Review of Fluorescent Tools for Live-Cell Imaging
    Specht, Elizabeth A.
    Braselmann, Esther
    Palmer, Amy E.
    ANNUAL REVIEW OF PHYSIOLOGY, VOL 79, 2017, 79 : 93 - 117
  • [24] An introduction to the wound healing assay using live-cell microscopy
    Jonkman, James E. N.
    Cathcart, Judith A.
    Xu, Feng
    Bartolini, Miria E.
    Amon, Jennifer E.
    Stevens, Katarzyna M.
    Colarusso, Pina
    CELL ADHESION & MIGRATION, 2014, 8 (05) : 440 - 451
  • [25] A Trojan Horse for live-cell super-resolution microscopy
    Beliu, Gerti
    Sauer, Markus
    LIGHT-SCIENCE & APPLICATIONS, 2020, 9 (01)
  • [26] Correlation of live-cell imaging with volume scanning electron microscopy
    Lucas, Miriam S.
    Gunthert, Maja
    Bittermann, Anne Greet
    de Marcox, Alex
    Wepf, Roger
    CORRELATIVE LIGHT AND ELECTRON MICROSCOPY III, 2017, 140 : 123 - 148
  • [27] Dihydro-Si-rhodamine for live-cell localization microscopy
    Zhang, Xiaodong
    Zhang, Mengmeng
    Yan, Yu
    Wang, Mingkang
    Li, Jin
    Yu, Yang
    Xiao, Yi
    Luo, Xiao
    Qian, Xuhong
    Yang, Youjun
    CHEMICAL COMMUNICATIONS, 2021, 57 (61) : 7553 - 7556
  • [28] Live-cell photoactivated localization microscopy of nanoscale adhesion dynamics
    Shroff, Hari
    Galbraith, Catherine G.
    Galbraith, James A.
    Betzig, Eric
    NATURE METHODS, 2008, 5 (05) : 417 - 423
  • [29] Chemogenetic Tags with Probe Exchange for Live-Cell Fluorescence Microscopy
    Iyer, Aditya
    Baranov, Maxim
    Foster, Alexander J.
    Chordia, Shreyans
    Roelfes, Gerard
    Vlijm, Rifka
    van den Bogaart, Geert
    Poolman, Bert
    ACS CHEMICAL BIOLOGY, 2021, 16 (05) : 891 - 904
  • [30] SRRF: Universal live-cell super-resolution microscopy
    Culley, Sian
    Tosheva, Kalina L.
    Pereira, Pedro Matos
    Henriques, Ricardo
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2018, 101 : 74 - 79