Tm. Reilly et al., SIMILARITIES IN THE PHENOTYPIC-EXPRESSION OF PERICYTES AND BONE-CELLS, Clinical orthopaedics and related research, (346), 1998, pp. 95-103
Bovine brain microvessel pericytes, bone cells, and fibroblasts were g
rown in tissue culture in 3%, 21%, or 60% oxygen for 7 weeks. Alkaline
phosphatase activity was highest in bone cells and pericytes grown in
3% oxygen, with the activity higher in the former than the latter. Al
kaline phosphatase activity was very low in fibroblasts at every oxyge
n concentration. Osteocalcin concentration was higher in bone cells th
an in pericytes, was not detected in fibroblasts, and in bone cells an
d pericytes the concentration was highest in 21% oxygen. Other bovine
brain microvessel pericytes were grown in 3% or 21% oxygen for 3 to 24
days in the presence or absence of bone morphogenetic protein 2 and i
n the presence or absence of parathyroid hormone. At Day 3 of culture,
alkaline phosphatase activity was highest in 21% oxygen in the presen
ce of bone morphogenetic protein 2. By Day 17 of culture, alkaline pho
sphatase activity was highest in 3% oxygen whether bone morphogenetic
protein was present or not. Cyclic adenosine monophosphate production
in pericytes in response to parathyroid hormone stimulation was very m
odest when compared with that of bone cells, and this response was not
found to be significantly altered by bone morphogenetic protein 2, du
ration of culture, or the oxygen concentration during incubation. Thes
e findings show that the microvessel pericyte is capable of exhibiting
several oxygen dependent, phenotypic characteristics ascribed to oste
oblasts.