Chapter 8 Monitoring Starvation-Induced Reactive Oxygen Species Formation

Methods in Enzymology

Volumn 451, Issue C, 2009, Pages 119-130

  Scherz Shouval, Ruth ^a   Elazar, Zvulun ^a  

^a WEIZMANN INSTITUTE OF SCIENCE   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLCYSTEINE; CATALASE; REACTIVE OXYGEN METABOLITE; ANTIOXIDANT; FLUORESCENT DYE;

ANIMAL; ARTICLE; AUTOPHAGY; CELL LINE; CELL STRAIN COS1; CERCOPITHECUS; CHO CELL; CRICETULUS; HAMSTER; HELA CELL; HUMAN; METABOLISM; MOUSE; OXIDATIVE STRESS; PHYSIOLOGY; CELL DEATH; CELL ORGANELLE; CELL SURVIVAL; FLUOROMETRY; KINETICS; MICROSCOPY; MONITORING; PRIORITY JOURNAL; PROTEIN DEGRADATION; QUALITATIVE ANALYSIS; QUANTITATIVE ANALYSIS; REVIEW; SIGNAL TRANSDUCTION; STARVATION;

ACETYLCYSTEINE; ANIMALS; AUTOPHAGY; CATALASE; CELL LINE; CERCOPITHECUS AETHIOPS; CHO CELLS; COS CELLS; CRICETINAE; CRICETULUS; HELA CELLS; HUMANS; MICE; OXIDATIVE STRESS; REACTIVE OXYGEN SPECIES;

EID: 59249083454     PISSN: 00766879     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0076-6879(08)03608-2     Document Type: Review

References (36)

1. Adam-Vizi V., and Chinopoulos C. Bioenergetics and the formation of mitochondrial reactive oxygen species. Trends Pharmacol. Sci. 27 (2006) 639-645
2. Bedard K., and Krause K.H. The NOX family of ROS-generating NADPH oxidases: Physiology and pathophysiology. Physiol. Rev. 87 (2007) 245-313
3. Cathcart R., Schwiers E., and Ames B.N. Detection of picomole levels of hydroperoxides using a fluorescent dichlorofluorescein assay. Anal. Biochem. 134 (1983) 111-116
4. Chen Y., McMillan-Ward E., Kong J., Israels S.J., and Gibson S.B. Mitochondrial electron-transport-chain inhibitors of complexes I and II induce autophagic cell death mediated by reactive oxygen species. J. Cell Sci. 120 (2007) 4155-4166
5. Cuervo A.M., and Dice J.F. A receptor for the selective uptake and degradation of proteins by lysosomes. Science 273 (1996) 501-503
6. Dice J.F. Peptide sequences that target cytosolic proteins for lysosomal proteolysis. Trends Biochem. Sci. 15 (1990) 305-309
7. Djavaheri-Mergny M., Amelotti M., Mathieu J., Besancon F., Bauvy C., Souquere S., Pierron G., and Codogno P. NF-kB activation represses tumor necrosis factor-alpha-induced autophagy. J. Biol. Chem. 281 (2006) 30373-30382
8. Edens W.A., Sharling L., Cheng G., Shapira R., Kinkade J.M., Lee T., Edens H.A., Tang X., Sullards C., Flaherty D.B., Benian G.M., and Lambeth J.D. Tyrosine cross-linking of extracellular matrix is catalyzed by Duox, a multidomain oxidase/peroxidase with homology to the phagocyte oxidase subunit gp91phox. J. Cell Biol. 154 (2001) 879-891
9. Finn P.F., and Dice J.F. Ketone bodies stimulate chaperone-mediated autophagy. J. Biol. Chem. 280 (2005) 25864-25870
10. Gomez-Santos C., Ferrer I., Santidrian A.F., Barrachina M., Gil J., and Ambrosio S. Dopamine induces autophagic cell death and α-synuclein increase in human neuroblastoma SH-SY5Y cells. J. Neurosci. Res. 73 (2003) 341-350
11. Hafer K., Iwamoto K.S., and Schiestl R.H. Refinement of the dichlorofluorescein assay for flow cytometric measurement of reactive oxygen species in irradiated and bystander cell populations. Radiat. Res. 169 (2008) 460-468
12. Ichimura H., Parthasarathi K., Quadri S., Issekutz A.C., and Bhattacharya J. Mechano-oxidative coupling by mitochondria induces proinflammatory responses in lung venular capillaries. J. Clin. Invest. 111 (2003) 691-699
13. Iwai K., Kondo T., Watanabe M., Yabu T., Kitano T., Taguchi Y., Umehara H., Takahashi A., Uchiyama T., and Okazaki T. Ceramide increases oxidative damage due to inhibition of catalase by caspase-3-dependent proteolysis in HL-60 cell apoptosis. J. Biol. Chem. 278 (2003) 9813-9822
14. Kiffin R., Bandyopadhyay U., and Cuervo A.M. Oxidative stress and autophagy. Antioxid. Redox. Signal 8 (2006) 152-162
15. Kiffin R., Christian C., Knecht E., and Cuervo A.M. Activation of chaperone-mediated autophagy during oxidative stress. Mol. Biol. Cell 15 (2004) 4829-4840
16. Kirkland R.A., Adibhatla R.M., Hatcher J.F., and Franklin J.L. Loss of cardiolipin and mitochondria during programmed neuronal death: Evidence of a role for lipid peroxidation and autophagy. Neuroscience 115 (2002) 587-602
17. Kissova I., Deffieu M., Manon S., and Camougrand N. Uth1p is involved in the autophagic degradation of mitochondria. J. Biol. Chem. 279 (2004) 39068-39074
18. Kissova I., Deffieu M., Samokhvalov V., Velours G., Bessoule J.J., Manon S., and Camougrand N. Lipid oxidation and autophagy in yeast. Free Radic. Biol. Med. 41 (2006) 1655-1661
19. Lambeth J.D. NOX enzymes and the biology of reactive oxygen. Nat. Rev. Immunol. 4 (2004) 181-189
20. Peng I T., and Jou M.J. Mitochondrial swelling and generation of reactive oxygen species induced by photoirradiation are heterogeneously distributed. Ann. N.Y. Acad. Sci. 1011 (2004) 112-122
21. Preston T.J., Müller W.J., and Singh G. Scavenging of extracellular H2O2 by catalase inhibits the proliferation of HER-2/Neu-transformed rat-1 fibroblasts through the induction of a stress response. J. Biol. Chem. 276 (2001) 9558-9564
22. Reef S., Zalckvar E., Shifman O., Bialik S., Sabanay H., Oren M., and Kimchi A. A short mitochondrial form of p19ARF induces autophagy and caspase-independent cell death. Mol. Cell 22 (2006) 463-475
23. Sakurai K., and Cederbaum I A. Oxidative stress and cytotoxicity induced by ferric-nitrilotriacetate in HepG2 cells that express cytochrome P450 2E1. Mol. Pharmacol. 54 (1998) 1024-1035
24. Scherz-Shouval R., and Elazar Z. ROS, mitochondria and the regulation of autophagy. Trends Cell Biol. 17 (2007) 422-427
25. Scherz-Shouval R., Shvets E., Fass E., Shorer H., Gil L., and Elazar Z. Reactive oxygen species are essential for autophagy and specifically regulate the activity of Atg4. EMBO J. 26 (2007) 1749-1760
26. Shvets E., Fass E., and Elazar Z. Utilizing flow cytometry to monitor autophagy in living mammalian cells. Autophagy 4 (2008) 621-628
27. Suh Y.A., Arnold R.S., Lassegue B., Shi J., Xu X., Sorescu D., Chung A.B., Griendling K.K., and Lambeth J.D. Cell transformation by the superoxide-generating oxidase Mox1. Nature 401 (1999) 79-82
28. Tasdemir E., Galluzzi L., Maiuri M.C., Criollo A., Vitale I., Hangen E., Modjtahedi N., and Kroemer G. Methods for assessing autophagy and autophagic cell death. Methods Mol. Biol. 445 (2008) 29-76
29. Vanden Hoek T.L., Li Z., Shao, Schumacker P.T., and Becker L.B. Significant levels of oxidants are generated by isolated cardiomyocytes during ischemia prior to reperfusion. J. Mol. Cell Cardiol. 29 (1997) 2571-2583
30. Xiong Y., Contento A.L., Nguyen P.Q., and Bassham D.C. Degradation of oxidized proteins by autophagy during oxidative stress in Arabidopsis. Plant. Physiol. 143 (2007) 291-299
31. 2. Free Radic. Biol. Med. 34 (2003) 1531-1543
32. Xu Y., Kim S.O., Li Y., and Han J. Autophagy contributes to caspase-independent macrophage cell death. J. Biol. Chem. 281 (2006) 19179-19187
33. Xue L., Fletcher G.C., and Tolkovsky A.M. Autophagy is activated by apoptotic signalling in sympathetic neurons: An alternative mechanism of death execution. Mol. Cell Neurosci. 14 (1999) 180-198
34. Yu L., Wan F., Dutta S., Welsh S., Liu Z., Freundt E., Baehrecke E.H., and Lenardo M. Autophagic programmed cell death by selective catalase degradation. Proc. Natl. Acad. Sci. USA 103 (2006) 4952-4957
35. Zhu H., Bannenberg G.L., Moldeus P., and Shertzer H.G. Oxidation pathways for the intracellular probe 2′,7′-dichlorofluorescein. Arch. Toxicol. 68 (1994) 582-587
36. Zorov D.B., Filburn C.R., Klotz L.O., Zweier J.L., and Sollott S.J. Reactive oxygen species (ROS)-induced ROS release: A new phenomenon accompanying induction of the mitochondrial permeability transition in cardiac myocytes. J. Exp. Med. 192 (2000) 1001-1014