Primary bovine osteoclasts were obtained by an outgrowth method from b
ovine periosteum and cultured for 7 days on an ionomeric cement for bi
omaterial testing. Osteoclasts cultured on slices of bovine bone and o
n glass microscope cover-slides served as a control. The cells were ch
aracterised as osteoclasts by a number of tests. Osteoclasts showed po
sitive staining for tartrate resistant acid phosphatase and reactivity
with the antibodies 13C2 and 23C6, which react with the alpha-chain o
f the vitronectin receptor. Addition of salmon calcitonin to the cultu
re medium led to sudden cessation of lamellipodial activity. The cells
resorbed bone by making pits. In mixed cultures with osteoblasts, the
morphology of the osteoclasts on the smooth ionomeric cement surface
was comparable to the one on glass cover-slides, revealing broad cytop
lasmatic extensions on the material. Acridine orange staining demonstr
ated viability of cells until the end of the culture period and increa
sed acidification after parathyroid hormone (PTH) stimulation. Scannin
g electron microscopy did not reveal erosion of the material by osteoc
lasts. No signs of aluminium toxicity on osteoclasts could be detected
during the 7 day culture period, although an increased uptake of alum
inium into the cell was demonstrated.