Redox Biology Center, University of Nebraska-Lincoln, Lincoln, NE 68583, USA.
Antioxid Redox Signal. 2012 Dec 15;17(12):1694-713. doi: 10.1089/ars.2012.4553. Epub 2012 Jul 16.
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).
There is increasing evidence demonstrating that GSH loss is an active phenomenon regulating the redox signaling events modulating cell death activation and progression.
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.
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.
谷胱甘肽 (GSH) 的消耗是调节细胞死亡途径激活的中心信号事件。GSH 的消耗通常被视为氧化应激的标志物,因此,由于其抗氧化特性,它可以清除氧和氮的活性物质 (ROS/RNS)。
越来越多的证据表明,GSH 的损失是一种调节氧化还原信号事件的主动现象,这些事件调节细胞死亡激活和进展中的细胞还原平衡的改变。
在这项工作中,我们通过 GSH 的外排来综述 GSH 消耗的作用,这是一个重要事件,可调节细胞死亡过程中独立于氧化应激和 ROS/RNS 形成的细胞氧化还原平衡的改变。我们讨论了细胞死亡进展过程中 GSH 外排所涉及的机制,以及 GSH 消耗调节细胞死亡机制激活的氧化还原信号事件。
这里总结的证据清楚地将 GSH 转运作为介导细胞死亡过程中氧化还原信号的中心机制。未来的研究应该致力于确定介导细胞死亡过程中 GSH 外排的 GSH 转运体的分子特征,并解决缺乏定量 GSH 外排的敏感方法的问题。