Abstract
Selenium and mercuric chloride (MC) interactions regarding effects on cell growth and cell death have been studied. Human K-562 cells were pretreated or simultaneously treated with either selenite (5 or 50 µM) or selenomethionine (10 or 50 µM) and with MC (35 or 50 µM). The 35-µM MC treatments resulted in a clear inhibition of cell growth with no obvious difference between mercury-treated and mercury-selenium-treated cells. Furthermore, the apoptotic frequency was similar at all observations for all selenium treatments with 35 µM MC. In the simultaneously treated selenite and 50-µM MC combinations, a selenite-dependent protection was shown both by increased cell growth and by lower apoptotic frequency at 48 and 96 h of exposure. Both treatments with selenomethionine showed protection observed as an increased cell growth at 48 and 96 h and as decreased apoptotic frequency at 96 h of exposure.
Similar content being viewed by others
References
S. D. Potter and G. Matrone, A tissue culture model for mercury-selenium interactions, Toxicol. Appl. Pharmacol. 40, 201–215 (1977).
A. Naganuma and N. Imura, Changes in in vitro interaction profiles of mercuric mercury and selenite in rabbit blood under various reaction conditions, J. Pharmacobio-Dynam. 6, 331–339 (1983).
Y. Mochizuki, T. Kobayashi, and R. Doi, Comparison of cytotoxicity of mercury-selenium and mercury compounds on cultured cells, Toxicol. Lett. 22, 47–51 (1984).
C. Sasakura and K. T. Suzuki, Biological interaction between transition metals (Ag, Cd and Hg), selenide/sulfide and selenoprotein P, J. Inorg. Biochem. 71, 159–162 (1998).
N. Imura and A. Naganuma, Possible mechanism of detoxifying effect of selenium on the toxicity of mercury compounds, in Advances in Mercury Toxicology, T. Suzuki, N. Imura, and T. Clarkson, eds., Plenum, New York, pp. 275–288 (1991).
J. B. Nielsen and O. Andersen, A comparison of the effects of sodium selenite and seleno-l-methionine on disposition of orally administered mercuric chloride, J. Trace Elements Electrolytes Health Dis. 5, 245–250 (1991).
U. Lindh, A. Danersund, and A. Lindvall, Selenium protection against toxicity from cadmium and mercury studied at the cellular level, Cell. Mol. Biol. (Noisy-le-grand) 42, 39–48 (1996).
K. T. Suzuki, C. Sasakura, and S. Yoneda, Binding sites for the (Hg-Se) complex on selenoprotein P, Biochim. Biophys. Acta 1429, 102–112 (1998).
A. Naganuma, S. K. Pan, and N. Imura, In vitro studies on interaction of mercuric mercury and selenite in rabbit blood, Res. Commun. Chem. Pathol. Pharmacol. 20, 139–156 (1978).
A. Naganuma and N. Imura, Changes in distribution of mercury and selenium in soluble fractions of rabbit tissues after simultaneous administration, Pharmacol. Biochem. Behav 13, 537–544 (1980).
A. Naganuma, Y. Ishii, and N. Imura, Effect of administration sequence of mercuric chloride and sodium selenite on their fates and toxicities in mice, Ecotoxicol. Environ. Safety. 8, 572–580 (1984).
L. Magos, T. W. Clarkson, and A. R. Hudson, Differences in the effects of selenite and biological selenium on the chemical form and distribution of mercury after the simultaneous administration of HgCl2 and selenium to rats, J. Pharmacol. Exp. Ther. 228, 478–483 (1984).
L. Magos, T. W. Clarkson, S. Sparrow, et al., Comparison of the protection given by selenite, selenomethionine and biological selenium against the renotoxicity of mercury, Arch. Toxicol. 60, 422–426 (1987).
S. C. Fang, Interaction of selenium and mercury in the rat, Chem. Biol. Interact. 17, 25–40 (1977).
P. Frisk, A. Yaqob, K. Nilsson, et al., Differences in the growth inhibition of cultured K-562 cells by selenium, mercury or cadmium in two tissue culture media (RPMI-1640, Ham’s F-10), Biometals 13, 101–111 (2000).
P. Frisk, A. Yaqob, K. Nilsson, et al., Influence of selenium on mercuric chloride cellular uptake and toxicity indicating protection. Studies on cultured K-562 cells., Biol. Trace Element Res. 81, 229–244 (2001).
C. B. Lozzio and B. B. Lozzio, Human chronic myelogenous leukemia cell-line with positive Philadelphia chromosome, Blood 45, 321–334 (1975).
L. C. Andersson, K. Nilsson, and C. G. Gahmberg, K562—a human erythroleukemic cell line, Int. J. Cancer 23, 143–147 (1979).
J. Tennant, Evaluation of the trypan blue technique for determination of cell viability, Transplantation 2(6), 685–694 (1964).
A. A. Akhand, M. Kato, H. Suzuki, et al., Level of HgCl2-mediated phosphorylation of intracellular proteins determines death of thymic T-lymphocytes with or without DNA fragmentation, J Cell Biochem. 71, 243–253 (1998).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Frisk, P., Wester, K., Yaqob, A. et al. Selenium protection against mercury-induced apoptosis and growth inhibition in cultured K-562 cells. Biol Trace Elem Res 92, 105–113 (2003). https://doi.org/10.1385/BTER:92:2:105
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1385/BTER:92:2:105