Effect of cellular glutathione depletion on cadmium-induced cytotoxicity in human lung carcinoma cells

Cell Biology and Toxicology - Tập 3 - Trang 347-360 - 1987
Yu -Jian Kang1, M. Duane Eenger1
1Department of Zoology, Iowa State University, Ames, USA

Tóm tắt

The effect of glutathione depletion on cellular toxicity of cadmium was investigated in a subpopulation (T27) of human lung carcinoma A549 cells with coordinately high glutathione levels and Cd++-resistance. Cellular glutathione levels were depleted by exposing the cells to diethyl maleate or buthionine sulfoximine. Depletion was dose-dependent. Exposure of the cells to 0.5 mM diethyl maleate for 4 hours or to 10 mM buthionine sulfoximine for 8 hours eliminated the threshold for Cd++ cytotoxic effect and deccreased the LD50S. Cells that were pretreated with 0.5 mM diethyl maleate or 10 mM buthionine sulfoximine and then exposed to these same concentrations of diethyl maleate or buthionine sulfoximine during the subsequent assay for colony forming efficiency produced no colonies, reflecting an enhanced sensitivity to these agents at low cell density. Diethyl maleate was found to be more cytotoxic than buthionine sulfoximine. Synergistic cytotoxic effects were observed in the response of diethyl maleate pretreated cells exposed to Cd++. Thus the results demostrated that depletion of most cellular glutathione in A549-T27 cells prior to Cd++ exposure sensitizes them to the agent's cytotoxic effects. Glutathione thus may be involved in modulating the early cellular Cd++ cytotoxic response. Comparison of reduced glutathione levels and of Cd++ cytotoxic responses in buthionine sulfoximine-treated A549-T27 cells with those levels in other, untreated normal and tumor-derived cells suggests that the higher level of glutathione in A549-T27 is not the sole determinant of its higher level of Cd++ resistance.

Tài liệu tham khảo

ANDERSON, M.E. (1985). Detremination of glutathione and glutathione disulfide in biological samples. Method Enzymo. 113:548–555. BRODIE, A.E. and REED, D.J. (1985). Buthionine sulfoximine inhibition of cystine uptake and glutathione biosynthesis in human lung carcinoma cells. Toxicol. Appl. Phramacol. 77:381–387. BRUNING, J.L. and KINTZ, B.L. (1977). Computational Handbook of Statistics, pp. 116–131. Scott, Foresman and Company, Glenview, Illinois. DE GRAFF, W.G. and MITCHELL, J.B. (1985). Glutathione dependence of neocarzinostatin cytotoxicity and mutagenicity in Chinese hamster V-79 cells. Cancer Res. 45:4760–4762. EENGER, M.D., HILDERBRAND, C.E., WALTERS, R.A, SEARGRAVE, J.C., BARHAM, S.S. and HOAGLUND, H.C. (1984). Molecular and somatic cell genetic analysis of metal resistance mechanisms in mammalian cells. In: Molecular and Cellular Approaches to Understanding Mechanisms of Toxicity. (A.H. Tashjian ed.) pp. 38–62. Published by the Harvard School of Public Health. EENGER, M.D., TESMER, J.G., TRABVIS, G.L. and BARHAM, S.S> (1986a). Clonal variation of cadmium response in human tumor cell lines. Am. J. Physiol. 250 (Cell Physiol. 19):C256-C263. EENGER, M.D., HILDERBRAND, C.E., SEARGRAVE, J.C. and TOBEY, R.A. (1986b). Cellular resistance to cadmium. In: Handbook of Experimental Pharmacology, Vol. 80 (E.C. Foulkes ed.) pp. 363–396. Published by Springer-Verlag. FREEMAN, M.L., MALCOLM, A.W. and MEREDITH, J.J. (1985). Role of glutathione in cell survival after hyperthermic treatment of Chinese hamster ovary cells. Cancer Res. 45:6308–6313. KETTER, B. (1982). The role of nonenzymatic reactions of glutathione in xenobiotic metabolism. Drug Metabolism Rev. 13(1):161–187. MEISTER, A. (1985). Methods for the selective modification of glutathione metabolism and study of glutathione transport. Methods Enzymol. 113:571–585. MITCHELL, J.B., RUSSO, A., KINSELLA, T.J. and GLATSTEIN, E. (1983). Glutathione elevation during thermotolerance induction and thermosensitization by glutathione depletion. Cancer Res. 43:987–991. MITCHELL, J.B., RUSSO, A., BIGALOW, J.E. and McPHERSON, S. (1983). Cellular glutathione depletion by diethyl maleate or buthionine sulfoximine: no effect of glutathione on the depletion on the oxygen enhancement ratio. Radiation Res. 96:422–428. REED, D.J. (1984). Cellular defense mechanisms against reactive metabolites. In: Bioactivation of Foreign Compounds (M. W. Anders, ed.) Academic Press, New York. RICHMAN, P.G. and MEISTER, A. (1975). Regulation of γ-glutamyl-cysteine synthesis by nonallosteric feedback inhibition by glutathione. J. Biol. Chem. 250:1422–1426. ROIZIN-TOWLE, L. (1985). Selective enhancement of hypoxic cell killing by melphalan via thiol depletuion: in vitro studies with hypoxic cell sensitizers and buthionine sulfoximine. J. Natl. Cancer Inst. 74:151–157. RUSSO, A., MITCHELL, J.B. and McPHERSON, S. (1984). The effects of glutathione depletion on thermotolerance and heat. Stress protein synthesis. Brit. J. Cancer 49:753–758. RUSSO, A. and MITCHELL, J.B. (1984). Radiation response of Chinese hamster cells after elevation of intracellular glutathione levels. Int. J. Radiat. Oncol. Biol. Phys. 10:1243–1247. RUSSO, A., DeGRAFF, W., FRIEDMAN, N. and MITCHELL, J.B. (1986). Selective modulation of glutathione levels in human normal versus tumor cells and subsequent differential response to chemotherapeutic drugs. Cancer Res. 46:2845–2848. SEAGRAVE, J.C., HILDEBRAND, C.E. and ENGER, M.D. (1983). Effects of cadmium on glutathione metabolism in cadmium sensitive and cadmium resistant Chinese hamster cell lines. Toxicol. 29:101–107. SHRIEVE, D.L., LI, G.C., ASTROMOFF, A. and HARRIS, J. (1986). Cellular glutathione, thermal sensitivity, and thermotolerance in Chinese hamster fibroblasts and their heat-resistant variants. Cancer Res. 46:1684–1685. ZAR, J.H. (1984). Biostatistical analysis. pp. 306–326. Prentice-Hall, Inc., Englewood Cliffs, New Jersey.