Rat bone marrow cells were cultured in experimental conditions that fa
vour the proliferation and differentiation of osteoblastic cells (i.e.
, 2.52 x 10(-4) mol l(-1) ascorbic acid, 10(-2) mol l(-1) beta-glycero
phosphate and 10(-8) mol l(-1) dexamethasone) in the absence and in th
e presence of stainless-steel corrosion products, for a period of 18 d
ays. An AISI 316L stainless-steel slurry (SS) was obtained by electroc
hemical means and the concentrations of the major metal ions, determin
ed by atomic absorption spectrometry, were 8.78 x 10(-3) mol l(-1) of
Fe, 4.31 x 10(-3) mol l(-1) of Cr and 2.56 x 10(-3) mol l(-1) of Ni. B
one marrow cells were exposed to 0.01, 0.1 and 1% of the SS and at the
end of the incubation period, control and treated cultures were evalu
ated by histochemical assays for the identification of the presence of
alkaline phosphatase and also calcium and phosphate deposition. Cultu
res were further observed by scanning electron microscopy. Levels of t
otal and ionised calcium and phosphorus in the culture media collected
from control and metal exposed cell cultures were also quantified. Hi
stochemical staining showed that control cultures presented a strong r
eaction for the presence of alkaline phosphatase and exhibited formati
on of calcium and phosphates deposits. The presence of 0.01% SS caused
no detectable biological effects in these cultures, 0.1% SS impaired
osteoblastic behaviour and, 1% SS resulted in cell death. In the absen
ce of bone cells, levels of total and ionised calcium and phosphorus i
n the control and metal added culture medium were similar throughout t
he incubation period. A significant decrease in the levels of ionised
calcium and phosphorus were observed in the culture medium of control
cultures and also in cultures exposed to 0.01% SS after two weeks of i
ncubation, an event related with the formation of mineral calcium phos
phate deposits in these cultures. In cultures grown in the presence of
0.1 and 1% SS corrosion products, levels of calcium and phosphorus we
re similar to those observed in the absence of cells. Results showed t
hat stainless-steel corrosion products above certain concentrations ma
y disturb the normal behaviour of osteoblast-like rat bone marrow cell
cultures. (C) 1998 Published by Elsevier Science Ltd. All rights rese
rved.