Mln. Diaz et al., EFFECT OF DESFERRIOXAMINE AND DEFERIPRONE (L1) ON THE PROLIFERATION OF MG-63 BONE-CELLS AND ON PHOSPHATASE ALKALINE ACTIVITY, Nephrology, dialysis, transplantation, 13, 1998, pp. 23-28
In the present work, we studied: (i) the effect of different doses of
desferrioxamine and deferiprone on the proliferation of osteoblasts an
d the possible role of iron in this; and (ii) the effect of both chela
tors on the metabolic activity of these cells, using the quantificatio
n of alkaline phosphatase as an enzymatic marker of cellular activity
or differentiation. Cellular proliferation was investigated at differe
nt concentrations of deferiprone and desferrioxamine, and the effect o
f the addition of iron citrate on this proliferation was measured. The
production of alkaline phosphatase after incubation with deferiprone
(150 and 300 mu M) and desferrioxamine (20 and 100 mu M) was also stud
ied. Cellular proliferation was completely inhibited with 100 mu M of
desferrioxamine and 300 mu M of deferiprone. In both cases, this effec
t was corrected by means of co-incubation with iron citrate. In the se
cond phase, using the same dose that inhibited the proliferation, it w
as observed that after 24 h, both chelators slightly decreased alkalin
e phosphatase activity, while at 48 and 96 h they increased alkaline p
hosphatase activity. These results demonstrate that both desferrioxami
ne and deferiprone inhibit the proliferation of the osteoblast-like ce
ll line MG-63; the effect seems to be related to the chelation of some
fraction of available iron. In spite of the effect on bone cell proli
feration, the chelators do not impair cellular activity.