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细胞和组织样本中的氧和缺氧成像。

Imaging of oxygen and hypoxia in cell and tissue samples.

机构信息

School of Biochemistry and Cell Biology, University College Cork, Cavanagh Pharmacy Building, College Road, Cork, Ireland.

Institute for Regenerative Medicine, Sechenov University, Moscow, Russian Federation.

出版信息

Cell Mol Life Sci. 2018 Aug;75(16):2963-2980. doi: 10.1007/s00018-018-2840-x. Epub 2018 May 14.

Abstract

Molecular oxygen (O) is a key player in cell mitochondrial function, redox balance and oxidative stress, normal tissue function and many common disease states. Various chemical, physical and biological methods have been proposed for measurement, real-time monitoring and imaging of O concentration, state of decreased O (hypoxia) and related parameters in cells and tissue. Here, we review the established and emerging optical microscopy techniques allowing to visualize O levels in cells and tissue samples, mostly under in vitro and ex vivo, but also under in vivo settings. Particular examples include fluorescent hypoxia stains, fluorescent protein reporter systems, phosphorescent probes and nanosensors of different types. These techniques allow high-resolution mapping of O gradients in live or post-mortem tissue, in 2D or 3D, qualitatively or quantitatively. They enable control and monitoring of oxygenation conditions and their correlation with other biomarkers of cell and tissue function. Comparison of these techniques and corresponding imaging setups, their analytical capabilities and typical applications are given.

摘要

分子氧 (O) 是细胞线粒体功能、氧化还原平衡和氧化应激、正常组织功能和许多常见疾病状态的关键参与者。已经提出了各种化学、物理和生物学方法来测量、实时监测和成像细胞和组织中 O 浓度、减少的 O(缺氧)状态和相关参数。在这里,我们回顾了已建立和新兴的光学显微镜技术,这些技术允许可视化细胞和组织样本中的 O 水平,主要是在体外和离体,但也在体内环境下。具体示例包括荧光缺氧染色剂、荧光蛋白报告系统、磷光探针和不同类型的纳米传感器。这些技术允许在活组织或死后组织中以 2D 或 3D 形式进行 O 梯度的高分辨率映射,定性或定量。它们能够控制和监测氧合条件及其与细胞和组织功能的其他生物标志物的相关性。给出了这些技术和相应成像设置、它们的分析能力和典型应用的比较。

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