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Glutathione efflux and cell death

机译:谷胱甘肽外排与细胞死亡

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Significance: Glutathione (GSH) depletion is a central signaling event that regulates the activation of cell death pathways. GSH depletion is often taken as a marker of oxidative stress and thus, as a consequence of its antioxidant properties scavenging reactive species of both oxygen and nitrogen (ROS/RNS). Recent Advances: There is increasing evidence demonstrating that GSH loss is an active phenomenon regulating the redox signaling events modulating cell death activation and progression. Critical Issues: In this work, we review the role of GSH depletion by its efflux, as an important event regulating alterations in the cellular redox balance during cell death independent from oxidative stress and ROS/RNS formation. We discuss the mechanisms involved in GSH efflux during cell death progression and the redox signaling events by which GSH depletion regulates the activation of the cell death machinery. Future Directions: The evidence summarized here clearly places GSH transport as a central mechanism mediating redox signaling during cell death progression. Future studies should be directed toward identifying the molecular identity of GSH transporters mediating GSH extrusion during cell death, and addressing the lack of sensitive approaches to quantify GSH efflux.
机译:意义:谷胱甘肽(GSH)耗竭是调节细胞死亡途径激活的主要信号转导事件。谷胱甘肽耗竭经常被视为氧化应激的标志,因此,由于其抗氧化特性,可清除氧气和氮气中的活性物质(ROS / RNS)。最新进展:越来越多的证据表明,GSH丢失是一种调节氧化还原信号传导事件的活跃现象,可调节细胞死亡的活化和进程。关键问题:在这项工作中,我们回顾了GSH的外排作用,它是调节细胞死亡过程中细胞氧化还原平衡变化的重要事件,其独立于氧化应激和ROS / RNS的形成。我们讨论了细胞死亡进程中GSH外排的机制以及GSH耗竭调节细胞死亡机制激活的氧化还原信号传递事件。未来方向:这里总结的证据清楚地表明GSH转运是细胞死亡进程中介导氧化还原信号传导的主要机制。未来的研究应针对鉴定在细胞死亡期间介导GSH挤出的GSH转运蛋白的分子身份,并解决缺乏量化GSH外排的敏感方法的问题。

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