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
相关论文
共 260 条
  • [91] Cardiomyocyte apoptosis induced by short-term diabetes requires mitochondrial GSH depletion
    Ghosh, S
    Pulinilkunnil, T
    Yuen, G
    Kewalramani, G
    An, D
    Qi, D
    Abrahani, A
    Rodrigues, B
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2005, 289 (02): : H768 - H776
  • [92] Glutathione peroxidase-1 protects from CD95-induced apoptosis
    Gouazé, V
    Andrieu-Abadie, N
    Cuvillier, O
    Malagarie-Cazenave, S
    Frisach, MF
    Mirault, ME
    Levade, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (45) : 42867 - 42874
  • [93] Gouazé V, 2001, MOL PHARMACOL, V60, P488
  • [94] CFTR is the primary known apical glutathione transporter involved in cigarette smoke-induced adaptive responses in the lung
    Gould, Neal S.
    Min, Elysia
    Martin, Richard J.
    Day, Brian J.
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2012, 52 (07) : 1201 - 1206
  • [95] Subcellular compartmentalization of glutathione: Correlations with parameters of oxidative stress related to genotoxicity
    Green, Richard M.
    Graham, Mark
    O'Donovan, Michael R.
    Chipman, J. Kevin
    Hodges, Nikolas J.
    [J]. MUTAGENESIS, 2006, 21 (06) : 383 - 390
  • [96] Intracellular GSH Depletion Triggered Mitochondrial Bax Translocation to Accomplish Resveratrol-Induced Apoptosis in the U937 Cell Line
    Guha, Prasun
    Dey, Anindya
    Sen, Rupashree
    Chatterjee, Mitali
    Chattopadhyay, Subrata
    Bandyopadhyay, Sandip K.
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2011, 336 (01) : 206 - 214
  • [97] Organic anion transporting polypeptides of the OATP/SLC21 family:: phylogenetic classification as OATP/SLCO superfamily, new nomenclature and molecular/functional properties
    Hagenbuch, B
    Meier, PJ
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2004, 447 (05): : 653 - 665
  • [98] Glutathione export during apoptosis requires functional multidrug resistance-associated proteins
    Hammond, Christine L.
    Marchan, Rosemarie
    Krance, Suzanne M.
    Ballatori, Nazzareno
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (19) : 14337 - 14347
  • [99] Activation of plasma membrane reduced glutathione transport in death receptor apoptosis of HepG2 cells
    Hammond, CL
    Madejczyk, MS
    Ballatori, N
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 2004, 195 (01) : 12 - 22
  • [100] Hydrogen peroxide and redox modulation sensitize primary mouse hepatocytes to TNF-induced apoptosis
    Han, Derick
    Hanawa, Naoko
    Saberi, Behnam
    Kaplowitz, Neil
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2006, 41 (04) : 627 - 639