The purpose of the current study was to determine the timely ingrowth
of blood vessels associated with demineralized bone matrix (DBM) induc
ed osteogenesis. Critical-size (10 x 5mm), full thickness bony defects
in rabbit parietal bone were implanted with DBM. Histological and ult
rastructural changes were examined 1, 2, 3, 4, 5, 6, 7 and 14 days lat
er. Neovascularization was assessed by immunohistochemical staining fo
r factor VIII antigen (marker for vascular endothelium) and also confi
rmed by staining using pan-endothelial antibody (CD31) (a marker for e
ndothelium). Immunohistochemical evaluation revealed a positive staini
ng for CD31 and Factor VIII expressed by endothelial cells by day 3 po
st grafting. By day 4, small blood vessels were first seen budding fro
m host bed towards the grafted DBM. Ultrastructural identification of
cells in the early stages of healing revealed the presence of macropha
ges. The monocyte-derived macrophage appears to play a central role in
the repair process using DBM. Results of this study demonstrated a ra
pid vascularization during the DBM induced osteogenesis. This rapid va
scularization is vital to the healing and bone induction ability of th
e DBM.