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使用多光子显微镜观察肝脏的解剖学、生理学和药理学。

Visualizing liver anatomy, physiology and pharmacology using multiphoton microscopy.

作者信息

Wang Haolu, Liang Xiaowen, Gravot Germain, Thorling Camilla A, Crawford Darrell H G, Xu Zhi Ping, Liu Xin, Roberts Michael S

机构信息

Therapeutics Research Centre, School of Medicine, The University of Queensland, Princess Alexandra Hospital, Woolloongabba, QLD 4102, Australia.

Department of Pharmacy, University of Rennes 1, Ille-et-Vilaine, Rennes, 35043, France.

出版信息

J Biophotonics. 2017 Jan;10(1):46-60. doi: 10.1002/jbio.201600083. Epub 2016 Jun 17.

Abstract

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.

摘要

在过去几年中,多光子显微镜(MPM)在基础和临床肝脏研究中越来越受欢迎且应用广泛。这项技术能以较少的光漂白和光毒性深入观察活体组织,有助于我们更好地了解健康和患病肝脏中细胞形态、微环境、免疫反应以及药物和治疗性细胞的时空动态。本综述总结了MPM在肝病学中的原理、机遇、应用及局限性。重点强调了利用荧光寿命成像(FLIM)为肝脏内源性荧光物质以及体内应用于肝脏的外源性分子和纳米颗粒的检测增加额外的定量分析和特异性。我们预计在不久的将来,MPM-FLIM将推动我们对肝脏疾病细胞和分子机制的理解,并将从实验室到临床进行评估,实现人类肝脏疾病的实时组织学研究。

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