Viability of Saccharomyces cerevisiae cells following exposure to H2O2 and protective effect of minocycline depend on the presence of VDAC

European Journal of Pharmacology

Volumn 643, Issue 1, 2010, Pages 42-47

  Gałgańska, Hanna ^a   Karachitos, Andonis ^a   Baranek, Małgorzata ^a   Budzińska, Małgorzata ^a   Jordán, Joaquín ^b   Kmita, Hanna ^a  

^a ADAM MICKIEWICZ UNIVERSITY   (Poland)

^b UNIVERSITY OF CASTILLA LA MANCHA   (Spain)

Author keywords

Hydrogen peroxide; Minocycline; Saccharomyces cerevisiae; VDAC

Indexed keywords

HYDROGEN PEROXIDE; MINOCYCLINE; MITOCHONDRIAL PROTEIN; VOLTAGE DEPENDENT ANION CHANNEL 1;

ARTICLE; CELL GROWTH; CELL PROTECTION; CELL VIABILITY; CONTROLLED STUDY; CYTOSOL; MITOCHONDRION; NONHUMAN; OXIDATION REDUCTION STATE; PRIORITY JOURNAL; SACCHAROMYCES CEREVISIAE;

EID: 77955055915     PISSN: 00142999     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejphar.2010.06.033     Document Type: Article

References (42)

1. Akerboom T.P., Sies H. Assay of glutathione, glutathione disulfide, and glutathione mixed disulfides in biological samples. Methods Enzymol. 1981, 77:373-382.
2. Benz R. Permeation of hydrophylic solutes through mitochondrial outer membrane: review on mitochondrial porins. Biochim. Biophys. Acta 1994, 1197:167-196.
3. Blachly-Dyson E., Forte M. VDAC channels. IUBMB Life 2001, 52:113-118.
4. Blachly-Dyson E., Song J., Wolfgang W.J., Colombini M., Forte M. Multicopy suppressors of phenotype resulting from the absence of yeast VDAC encode a VDAC-like protein. Mol. Cell. Biol. 1997, 17:5727-5738.
5. Budzinska M., Galganska H., Wojtkowska M., Stobienia O., Kmita H. Effects of VDAC isoforms on CuZn-superoxide dismutase activity in the intermembrane space of Saccharomyces cerevisiae mitochondria. Biochem. Biophys. Res. Commun. 2007, 357:1065-1070.
6. Colombini M. VDAC: the channel at the interface between mitochondria and the cytosol. Mol. Cell. Biochem. 2004, 256-257:107-115.
7. Colombini M., Blachly-Dyson E., Forte M. VDAC, a channel in the outer mitochondrial membrane. Ion Channels 1996, 4:169-202.
8. Daroui P., Desai S.D., Li T.K., Liu A.A., Liu F. Hydrogen peroxide induces topoisomerase I-mediated DNA damage and cell death. J. Biol. Chem. 2004, 279:14587-14594.
9. Daum G., Bohni P.C., Schatz G. Import of proteins into mitochondria. Cytochrome b2 and cytochrome c peroxidase are located in the intermembrane space of yeast mitochondria. J. Biol. Chem. 1982, 257:13028-13033.
10. De Pinto V., Messina V., Accardi R., Aiello R., Guarino F., Tomasello M.F., Tommasino M., Tasco G., Casadio R., Benz R., De Giorgi F., Ichas F., Baker M., Lawen A. New functions of an old protein: the eukaryotic porin or voltage dependent anion selective channel (VDAC). Ital. J. Biochem. 2003, 52:17-24.
11. Galganska H., Budzinska M., Wojtkowska M., Kmita H. Redox regulation of protein expression in Saccharomyces cerevisiae mitochondria: possible role of VDAC. Arch. Biochem. Biophys. 2008, 479:39-45.
12. Galganska H., Karachitos A., Wojtkowska M., Stobienia O., Budzinska M., Kmita H. Communication between mitochondria and nucleus: putative role for VDAC in reduction/oxidation mechanism. Biochim. Biophys. Acta 2010, 1797:1276-1280.
13. Garcia-Martinez E.M., Sanz-Blasco S., Karachitos A., Bandez M.J., Fernandez-Gomez F.J., Perez-Alvarez S., de Mera R.M., Jordan M.J., Aguirre N., Galindo M.F., Villalobos C., Navarro N., Kmita H., Jordán J. Mitochondria and calcium flux as targets of neuroprotection caused by minocycline in cerebellar granule cells. Biochem. Pharmacol. 2010, 79:239-250.
14. Gieseler A., Schultze A.T., Kupsch K., Haroon M.F., Wolf G., Siemen D., Kreutzmann P. Inhibitory modulation of the mitochondrial permeability transition by minocycline. Biochem. Pharmacol. 2009, 77:888-896.
15. Grant C.M., MacIver F.H., Dawes I.W. Mitochondrial function is required for resistance to oxidative stress in the yeast Saccharomyces cerevisiae. FEBS Lett. 1997, 410:219-222.
16. Grant C.M., Perrone G., Dawes I.W. Glutathione and catalase provide overlapping defenses for protection against hydrogen peroxide in the yeast Saccharomyces cerevisiae. Biochem. Biophys. Res. Commun. 1998, 253:893-898.
17. Gupta S., Young T., Yel L., Su H., Gollapudi S. Differential sensitivity of naïve and subsets of memory CD4+ and CD8+ T cells to hydrogen peroxide-induced apoptosis. Genes Immun. 2007, 8:560-569.
18. Kmita H., Stobienia O., Michejda J. The access of metabolites into yeast mitochondria in the presence and absence of the voltage dependent anion selective channel (YVDAC1). Acta Biochim. Pol. 1999, 46:991-1000.
19. Kmita H., Budzińska M., Stobienia O. Modulation of the voltage-dependent anion-selective channel by cytoplasmic proteins from wild type and the channel depleted cells of Saccharomyces cerevisiae. Acta Biochim. Pol. 2003, 50:415-424.
20. Kroemer G., Galluzzi L., Brenner C. Mitochondrial membrane permeabilization in cell death. Physiol. Rev. 2007, 87:99-163.
21. Laloraya S., Gambill B.D., Craig E.A. A role for a eukaryotic GrpE-related protein, Mge1p, in protein translocation. Proc. Natl Acad. Sci. USA 1994, 91:6481-6485.
22. Lee A.C., Xu X., Blachly-Dyson E., Forte M., Colombini M. The role of yeast VDAC genes on the permeability of the mitochondrial outer membrane. J. Membr. Biol. 1998, 161:173-181.
23. Lemasters J.J., Holmuhamedov E. Voltage-dependent anion channel (VDAC) as mitochondrial governator-thinking outside the box. Biochim. Biophys. Acta 2006, 1762:181-190.
24. Liu H., Colavitti R., Rovira I.I., Finkel T. Redox-dependent transcriptional regulation. Circ. Res. 2005, 97:967-974.
25. Lord P.G., Wheals A.E. Asymmetrical division of Saccharomyces cerevisiae. J. Bacteriol. 1980, 142:808-818.
26. Madeo F., Fröhlich E., Ligr M., Grey M., Sigrist S.J., Wolf D.H., Fröhlich K.U. Oxygen stress: a regulator of apoptosis in yeast. J. Cell Biol. 1999, 145:757-767.
27. 2. Proteomics 2007, 7:1434-1445.
28. Mannella C.A., Kinnally C.W. Reflections on VDAC as a voltage-gated channel and a mitochondrial regulator. J. Bioenerg. Biomembr. 2008, 40:149-155.
29. Maris A.F., Assumpção A.L., Bonatto D., Brendel M., Henriques J.A. Diauxic shift-induced stress resistance against hydroperoxides in Saccharomyces cerevisiae is not an adaptive stress response and does not depend on functional mitochondria. Curr. Genet. 2001, 39:137-149.
30. O'Brien K.M., Dirmeier R., Engle M., Poyton R.O. Mitochondrial protein oxidation in yeast mutants lacking manganase-(MnSOD) or copper- and zinc-containing superoxide dismutase (CuZnSOD): evidence that MnSOD and CuZnSOD have both unique and overlapping functions in protecting mitochondrial proteins from oxidative damage. J. Biol. Chem. 2004, 279:51817-51827.
31. Pavlov E., Grigoriev S.M., Dejean L.M., Zweihorn C.L., Mannella C.A., Kinnally K.W. The mitochondrial channel VDAC has a cation-selective open state. Biochim. Biophys. Acta 2005, 1710:96-102.
32. Perrone G.G., Tan S.X., Dawes I.W. Reactive oxygen species and yeast apoptosis. Biochim. Biophys. Acta 2008, 1783:1354-1368.
33. Pesaresi P., Schneider A., Kleine T., Leister D. Interorganellar communication. Curr. Opin. Plant Biol. 2007, 10:600-606.
34. 2. Redox Rep. 2003, 8:371-377.
35. Shoshan-Barmatz V., Keinan N., Zaid H. Uncovering the role of VDAC in the regulation of cell life and death. J. Bioenerg. Biomembr. 2008, 40:183-191.
36. 2 protects Saccharomyces cerevisiae cells in stationary phase against oxidative stress. FEBS Lett. 2004, 578:152-156.
37. Stohs S.J., Bagchi D. Oxidative mechanisms in the toxicity of metal ions. Free Radic. Biol. Med. 1995, 18:321-336.
38. Sturtz L.A., Diekert K., Jensen L.T., Lill R., Culotta V.C. A fraction of yeast Cu, Zn-superoxide dismutase and its metallochaperone, CCS, localize to the intermembrane space of mitochondria. J. Biol. Chem. 2001, 276:38084-38089.
39. Thorpe G.W., Fong C.S., Alic N., Higgins V.J., Dawes I.W. Cells have distinct mechanisms to maintain protection against different reactive oxygen species: oxidative-stress-response genes. Proc. Natl. Acad. Sci. U.S.A. 2004, 101:6564-6569.
40. Vander Heiden M.G., Li X.X., Gottleib E., Hill R.B., Thompson C.B., Colombini M. Bcl-xL promotes the open configuration of the voltage-dependent anion channel and metabolite passage through the outer mitochondrial membrane. J. Biol. Chem. 2001, 276:19414-19419.
41. Woodson J.D., Chory J. Coordination of gene expression between organellar and nuclear genomes. Nat. Rev. Genet. 2008, 9:383-395.
42. 2-induced injury in SH-SY5Y cells. Neurochem. Res. 2009, 34:746-754.