Glutathione Efflux and Cell Death

被引:190
作者
Franco, Rodrigo [2 ]
Cidlowski, John A. [1 ]
机构
[1] NIEHS, Lab Signal Transduct, NIH, Res Triangle Pk, NC 27709 USA
[2] Univ Nebraska, Redox Biol Ctr, Sch Vet Med & Biomed Sci, Lincoln, NE 68583 USA
关键词
NECROSIS-FACTOR-ALPHA; MITOCHONDRIAL PERMEABILITY TRANSITION; MULTIDRUG-RESISTANCE PROTEIN-1; RECEPTOR-MEDIATED APOPTOSIS; FAS-INDUCED APOPTOSIS; CYTOCHROME-C RELEASE; B16; MELANOMA-CELLS; REACTIVE OXYGEN; OXIDATIVE STRESS; NITRIC-OXIDE;
D O I
10.1089/ars.2012.4553
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. Antioxid. Redox Signal. 17, 1694-1713.
引用
收藏
页码:1694 / 1713
页数:20
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