Developmentally, anatomically and histologically, bones are not all the sam
e. A number of studies over several years has raised the issue of osteoblas
t heterogeneity. These include observations on the diverse behavior of clon
al cell lines from both tumor and normal osteogenic tissue, on the heteroge
neous occurrence of disease in different parts of the skeleton, and on the
response of different parts of the skeleton to therapeutic interventions. M
ore recent observations on the biochemical make up of different bones and d
ifferent regions of bones and on the molecular profiles of osteoblasts asso
ciated with different skeletal sites are giving new insights. The accumulat
ing evidence indicates that osteoblasts in different maturational states, i
n different environments, and in different microenvironments, express diver
se gene repertoires. The diversity extends to expression of bone matrix mol
ecules, transcription factors, hormones and cytokines, and their receptors.
The data support the view that there is not a single unique phenotype char
acterizing all osteoblasts, but rather that different expressed gene repert
oires are associated with distinct osteoblast subpopulations and that this
molecular diversity may reflect a need for functional diversity in osteobla
sts engaged in different activities.