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Variability in sensitivity to arsenite does not correlate with arsenic accumulation rate in normal human lymphoblasts

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Abstract

Arsenic is a common environmental contaminant of our air, water and food, but not every individual who drinks arsenic-contaminated water shows clinical signs of toxicity. Large inter-individual variations are also found in arsenite-induced aneuploidy, chromosome aberrations and sister chromatid exchanges in peripheral blood lymphocytes from different human donors. Lymphoblasts are virally immortalized lymphocytes that retain most of the properties of lymphocytes. Individual lymphoblast cell lines retained their arsenite sensitivity after cryopreservation and subsequent revival. We measured the accumulation of 73[As]-arsenite into lymphoblast lines derived from 11 normal individuals. Arsenite accumulation rate varied 6.3 fold between the slowest and the fastest subjects. Assays in 14 lymphoblast lines showed variability to the toxic effects of arsenite, as measured by growth inhibition. Lymphoblast lines also vary with regard to their growth rates, but there is no relationship between growth rate and arsenite sensitivity. Surprisingly, we also found no correlation between arsenite accumulation rate and cellular sensitivity to growth inhibition, suggesting that the arsenite accumulation rate may not be the main determinant of cellular sensitivity to arsenic. We were also unable to detect evidence for a human homolog for the yeast arsenite efflux gene ACR3, using RT-PCR.

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References

  1. Leonard A: Arsenic. In: E. Merian (ed). Metals and Their Compounds in the Environment. VCH Publishers, New York, 1991, pp 751–774

    Google Scholar 

  2. National Research Council: Arsenic in Drinking Water. National Academy Press, Washington, DC, 1999, 263 pp

    Google Scholar 

  3. Rossman TG, Uddin AN, Burns FJ, Bosland MC: Arsenite is a cocarcinogen with solar ultraviolet radiation for mouse skin: An animal model for arsenic carcinogenesis. Toxicol Appl Pharmacol 176: 64–71, 2001

    Google Scholar 

  4. Lee TC, Ko JL, Jan KY: Differential cytotoxicity of sodium arsenite in human fibroblasts and Chinese hamster ovary cells. Toxicology 56: 289–299, 1989

    Google Scholar 

  5. Rossman TG, Goncharova EI, Rajah T, Wang Z: Human cells lack the inducible tolerance to arsenite seen in hamster cells. Mutat Res 386: 307–314, 1997

    Google Scholar 

  6. Wang Z, Rossman TG: Stable and inducible arsenite resistance in Chinese hamster cells. Toxicol Appl Pharmacol 118: 80–86, 1993

    Google Scholar 

  7. Chowdhury UK, Biswas BK, Chowdhury TR, Samanta G, Mandal BK, Basu GC, Chanda CR, Lodh D, Saha KC, Mukherjee SK, Roy S, Kabir S, Quamruzzaman Q, Chakraborti D: Groundwater arsenic contamination in Bangladesh and West Bengal, India. (comment). Environ Health Perspect 108: 393–397, 2000

    Google Scholar 

  8. Tondel M, Rahman M, Magnuson A, Chowdhury IA, Faruquee MH, Ahmad SA: The relationship of arsenic levels in drinking water and the prevalence rate of skin lesions in Bangladesh. Environ Health Perspect 107: 727–729, 1999

    Google Scholar 

  9. Crossen PE: Arsenic and SCE in human lymphocytes. Mutat Res 119: 415–419, 1983

    Google Scholar 

  10. Wiencke JK, Yager JW: Specificity of arsenite in potentiating cytogenetic damage induced by the DNA crosslinking agent diepoxybutane. Environ Mol Mutagen 19: 195–200, 1992

    Google Scholar 

  11. Vega L, Gonsebatt ME, Ostrosky-Wegman P: Aneugenic effect of sodium arsenite on human lymphocytes in vitro: An individual susceptibility effect detected. Mutat Res 334: 365–373, 1995

    Google Scholar 

  12. Ghosh M, Shen J, Rosen BP: Pathways of As (III) detoxification in Saccharomyces cerevisiae. Proc Natl Acad Sci USA 96: 5001–5006, 1999

    Google Scholar 

  13. Zhang X-Y, Ehrlich M: Detection and quantitation of low numbers of chromosomes containing bcl-2 oncogene translocations using seminested PCR. Biotechol Tech 16: 502–507, 1994

    Google Scholar 

  14. Rossman TG, Visalli MA, Uddin AN, Hu Y: Human cell models for arsenic carcinogenicity and toxicity: Transformation and genetic susceptibility. In: W.R. Chappell, C.O. Aberhathy, R.L. Calderon (eds). Arsenic Exposure and Health Effects IV. Elsevier Science, New York, 2001, pp 285–295

    Google Scholar 

  15. Silver S, Budd K, Leahy KM, Shaw WV, Hammond D, Novick RP, Willsky GR, Malamy MH, Rosenberg H: Inducible plasmid-determined resistance to arsenate, arsenite, and antimony (III) in Escherichia coli and Staphylococcus aureus. J Bacteriol 146: 983–996, 1981

    Google Scholar 

  16. Sanders OI, Rensing C, Kuroda M, Mitra B, Rosen BP: Antimonite is accumulated by the glycerol facilitator GlpF in Escherichia coli. J Bacteriol 179: 3365–3367, 1997

    Google Scholar 

  17. Borgnia M, Nielsen S, Engel A, Agre P: Cellular and molecular biology of the aquaporin water channels. Ann Rev Biochem 68: 425–458, 1999

    Google Scholar 

  18. Wysocki R, Chery CC, Wawrzycka D, Van Hulle M, Cornelis R, Thevelein JM, Tamas MJ: The glycerol channel Fps1p mediates the uptake of arsenite and antimonite in Saccharomyces cerevisiae. Mol Microbiol 40: 1391–1401, 2001

    Google Scholar 

  19. Liu Z, Shen J, Carbrey JM, Mukhopadhyay R, Agre P, Rosen BP: Arsenite transport by mammalian aquaglyceroporins AQP7 and AQP9. Proc Natl Acad Sci USA 99: 6053–6058, 2002

    Google Scholar 

  20. Bobrowicz P, Wysocki R, Owsianik G, Goffeau A, Ulaszewski S: Isolation of three contiguous genes, ACR1, ACR2 and ACR3, involved in resistance to arsenic compounds in the yeast Saccharomyces cerevisiae. Yeast 13: 819–828, 1997

    Google Scholar 

  21. Ishikawa T, Li ZS, Lu YP, Rea PA: The GS-X pump in plant, yeast, and animal cells: Structure, function, and gene expression. Biosci Rep 17: 189–207, 1997

    Google Scholar 

  22. Legare D, Cayer S, Singh AK, Richard D, Papadopoulou B, Ouellette M: ABC proteins of Leishmania. J Bioenerget Biomembr 33: 469–474, 2001

    Google Scholar 

  23. Cole SP, Sparks KE, Fraser K, Loe DW, Grant CE, Wilson GM, Deeley RG: Pharmacological characterization of multidrug resistant MRP-transfected human tumor cells. Cancer Res 54: 5902–5910, 1994

    Google Scholar 

  24. Styblo M, Del Razo LM, Vega L, Germolec DR, LeCluyse EL, Hamilton GA, Reed W, Wang C, Cullen WR, Thomas DJ: Comparative toxicity of trivalent and pentavalent inorganic and methylated arsenicals in rat and human cells. Arch Toxicol 74: 289–299, 2000

    Google Scholar 

  25. Wang TS, Kuo CF, Jan KY, Huang H: Arsenite induces apoptosis in Chinese hamster ovary cells by generation of reactive oxygen species. J Cell Physiol 169: 256–268, 1996

    Google Scholar 

  26. Jing Y, Dai J, Chalmers-Redman RM, Tatton WG, Waxman S: Arsenic trioxide selectively induces acute promyelocytic leukemia cell apoptosis via a hydrogen peroxide-dependent pathway. Blood 94: 2102–2111, 1999

    Google Scholar 

  27. Yi J, Gao F, Shi G, Li H, Wang Z, Shi X, Tang X: The inherent cellular level of reactive oxygen species: One of the mechanisms determining apoptotic susceptibility of leukemic cells to arsenic trioxide. Apoptosis 7: 209–215, 2002

    Google Scholar 

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Li, P., Uddin, A.N., Liu, Z. et al. Variability in sensitivity to arsenite does not correlate with arsenic accumulation rate in normal human lymphoblasts. Mol Cell Biochem 255, 79–85 (2004). https://doi.org/10.1023/B:MCBI.0000007263.27349.ae

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  • DOI: https://doi.org/10.1023/B:MCBI.0000007263.27349.ae

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