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    Visualizing liver anatomy, physiology and pharmacology using multiphoton microscopy

    Access Status
    Fulltext not available
    Authors
    Wang, H.
    Liang, X.
    Gravot, G.
    Thorling, C.
    Crawford, D.
    Xu, Z.
    Liu, Jian
    Roberts, M.
    Date
    2017
    Type
    Journal Article
    
    Metadata
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    Citation
    Wang, H. and Liang, X. and Gravot, G. and Thorling, C. and Crawford, D. and Xu, Z. and Liu, J. et al. 2017. Visualizing liver anatomy, physiology and pharmacology using multiphoton microscopy. Journal of Biophotonics. 10 (1): pp. 46-60.
    Source Title
    Journal of Biophotonics
    DOI
    10.1002/jbio.201600083
    ISSN
    1864-063X
    School
    WASM: Minerals, Energy and Chemical Engineering (WASM-MECE)
    URI
    http://hdl.handle.net/20.500.11937/70884
    Collection
    • Curtin Research Publications
    Abstract

    © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Multiphoton microscopy (MPM) has become increasingly popular and widely used in both basic and clinical liver studies over the past few years. This technology provides insights into deep live tissues with less photobleaching and phototoxicity, which helps us to better understand the cellular morphology, microenvironment, immune responses and spatiotemporal dynamics of drugs and therapeutic cells in the healthy and diseased liver. This review summarizes the principles, opportunities, applications and limitations of MPM in hepatology. A key emphasis is on the use of fluorescence lifetime imaging (FLIM) to add additional quantification and specificity to the detection of endogenous fluorescent species in the liver as well as exogenous molecules and nanoparticles that are applied to the liver in vivo. We anticipate that in the near future MPM-FLIM will advance our understanding of the cellular and molecular mechanisms of liver diseases, and will be evaluated from bench to bedside, leading to real-time histology of human liver diseases. (Figure presented.).

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