Effect of extracellular magnesium on topoisomerase II activity and expression in human leukemia HL-60 cells

Citation
V. Covacci et al., Effect of extracellular magnesium on topoisomerase II activity and expression in human leukemia HL-60 cells, J CELL BIOC, 78(2), 2000, pp. 325-333
Citations number
32
Categorie Soggetti
Cell & Developmental Biology
Journal title
JOURNAL OF CELLULAR BIOCHEMISTRY
ISSN journal
07302312 → ACNP
Volume
78
Issue
2
Year of publication
2000
Pages
325 - 333
Database
ISI
SICI code
0730-2312(200005)78:2<325:EOEMOT>2.0.ZU;2-L
Abstract
Topoisomerase II (TopoII) is a Mg-dependent enzyme involved in topological modifications of DNA that are crucial to the regulation of cell proliferati on and possibly differentiation. To investigate the role of Mg availability in the modulation of TopoII in whole cells, we studied enzyme activity and expression in HL-60 cells grown in the presence of decreasing amounts of e xtracellular Mg (0.5, 0.03, and 0.01 mM MgSO4). In comparison to cells grow n in 0.5 mM Mg, cells grown in 0.03 mM Mg exhibited a decrease in TopoII ac tivity, as evidenced by reduced induction of DNP/TopoII cleavable complexes and apoptosis by etoposide and teniposide. Enzyme activity was restored by the readdition of Mg (0.5 and 1.5 mM) in the incubation medium, confirming that this effect was indeed modulated by extracellular Mg. Restriction of Mg to 0.01 mM was associated with a dramatic decrease in TopoII activity re sembling that observed in HL-60 cells differentiated by dimethyl sulfoxide treatment. The restriction of Mg, while decreasing enzyme activity, was fou nd to upregulate TopoII protein expression, determined by Western blot anal ysis. The increase of TopoII protein levels was correlative with the degree of Mg deprivation. Collectively, these results indicate that extracellular levels of Mg may control availability of intracellular Mg, thus affecting the regulation of TopoII activity/expression and downstream processes of ce ll proliferation and/or differentiation. (C) 2000 Wiley-Liss, Inc.