This in vitro study was an investigation of osteoblast functions on gl
ass substrates modified with the bioactive peptide Arg-Gly-Asp-Ser (RG
DS) in the absence and presence of recombinant human Osteogenic Protei
n-1 (OP-1); control substrates were plain glass, glass modified with a
mine groups, and glass modified with the non-adhesive peptide Arg-Asp-
Gly-Ser. In serum-free cell culture medium, osteoblasts adhered in gre
ater numbers (P < 0.1) to glass modified with RGDS, compared to adhesi
on on all other substrate types tested in the present study. In the pr
esence of serum proteins, osteoblasts adhered similarly to all substra
te types examined, in the absence or presence of 100 ng ml(-1) OP-1. T
he presence of 100 ng ml(-1) OP-1 inhibited (P < 0.1) 72 h proliferati
on of sparsely seeded (2500 cells cm(-2)) cultures on all substrates e
xamined in the present study. OP-1 (100 ng ml(-1)) promoted 21 day min
eralization on all substrates examined; in addition, mineralization wa
s further enhanced in osteoblast cultures grown on glass modified with
the adhesive peptide RGDS. The present study establishes conditions w
hich can be utilized in the design of dental/orthopaedic biomaterials
which elicit timely, specific responses from surrounding bone tissue.