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Engineering of a near-infrared fluorescent probe for real-time simultaneous visualization of intracellular hypoxia and induced mitophagy

机译:近红外荧光探针的工程设计可实时同时可视化细胞内的缺氧和诱因的线粒体

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摘要

Mitophagy induced by hypoxia plays an important role in regulating cellular homeostasis via the removal of dysfunctional mitochondria in the lysosomal degradation pathway, which results in physiological changes in the mitochondria, such as the pH, polarity and viscosity. However, the lack of an effective method for imaging of both the hypoxic microenvironment and the resulting variable mitochondria limits the visualization of hypoxia-induced mitophagy. Based on the specific mitochondrial pH changes during the hypoxia-induced mitophagy process, we have reported a near-infrared fluorescent probe (NIR-HMA) for real-time simultaneous visualization of the hypoxic microenvironment and the subsequent mitophagy process in live cells. NIR-HMA selectively accumulated in the hypoxic mitochondria in the NIR-MAO form, emitting at 710 nm, and then transformed into NIR-MAOH, emitting at 675 nm, in the acidified mitochondria-containing autolysosomes. Importantly, by smartly tethering the hypoxia-responsive group to the hydroxyl group of the NIR-fluorochrome, which shows ratiometric pH changes, NIR-HMA can differentiate between different levels of the hypoxic microenvironment and mitophagy. Furthermore, using NIR-HMA, we could track the complete mitophagy process from the mitochondria to the autolysosomes and visualize mitophagy caused only by hypoxia both in cancer cells and normal cells. Finally, NIR-HMA was applied to investigate the role that mitophagy plays in the hypoxic microenvironment via the cycling hypoxia-reoxygenation model. We observed a decreased fluorescence ratio after reoxygenation and a further increased mitophagy level after hypoxia was induced again, suggesting that mitophagy might be a self-protective process that allows cells to adapt to hypoxia. Our work may provide an attractive way for real-time visualization of relevant physiological processes in hypoxic microenvironments.
机译:缺氧引起的线粒体吞噬通过消除溶酶体降解途径中功能异常的线粒体在调节细胞稳态中起着重要作用,从而导致线粒体的生理变化,例如pH,极性和粘度。但是,缺乏对缺氧的微环境和由此产生的可变的线粒体成像的有效方法,限制了低氧诱导的线粒体的可视化。基于缺氧诱导的线粒体过程中特定线粒体pH的变化,我们已经报道了一种近红外荧光探针(NIR-HMA),用于实时同时可视化低氧微环境和活细胞中的线粒体过程。 NIR-HMA选择性地以NIR-MAO形式蓄积在缺氧线粒体中,在710 nm处发射,然后转化为NIR-MAOH,在酸化的含线粒体自溶酶体中发射在675 nm处。重要的是,通过巧妙地将缺氧反应性基团束缚在NIR荧光染料的羟基上(显示比例pH值变化),NIR-HMA可以区分低氧微环境和线粒体的不同水平。此外,使用NIR-HMA,我们可以跟踪从线粒体到自体溶酶体的完整线粒体吞噬过程,并可视化癌细胞和正常细胞中仅由低氧引起的线粒体吞噬。最后,NIR-HMA通过循环缺氧-复氧模型研究了线粒体在缺氧微环境中的作用。我们观察到复氧后荧光比率降低,并且在再次诱导缺氧后线粒体水平进一步升高,这表明线粒体可能是一种自我保护过程,可使细胞适应缺氧。我们的工作可能会为低氧微环境中相关生理过程的实时可视化提供有吸引力的方法。

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