Current research is reviewed regarding the actions of three growth fac
tor systems on bone formation: insulin-like growth factors (IGFs), tra
nsforming growth factor-beta s (TGF beta s), and bone morphogenetic pr
oteins (BMPs). Each growth factor family consists of multiple related
growth factor genes. TGF beta s and BMPs 2-7 are subfamilies of a larg
er TGF beta superfamily. IGFs, TGF beta s and BMPs are produced by ost
eoblasts and other bone cells and affect osteoblast proliferation and
differentiation. They are also incorporated into mineralized bone matr
ix and retain activity when extracted from bone. Various hormones, gro
wth factors, and mechanical stress influence bone cell production of I
GFs, TGF beta s, and BMPs. Thus these growth factors may function in l
ocal regulation of bone formation. Currently there is much interest in
the function of IGF binding proteins, which are also produced by bone
cells, in regulating IGF activities in bone. Recently, mechanisms for
activation of the TGF beta serine/threonine kinase receptors have bee
n investigated, and receptors for BMPs have been identified which are
structurally related to TGF beta receptors. In vivo studies are discus
sed which demonstrate the applicability of IGFs, TGF beta s and BMPs t
o increasing bone formation systemically, promoting fracture healing a
nd inducing bone growth around implants.