Table 2. Effects of VEGF on intramembranous ossification.
Methods | Materials | Effects | References |
---|---|---|---|
In vivo | Rat tibial fracture defects | VEGF enhanced fracture bone repair | 49 |
Tibial cortical bone defects | Improved direct bone repair | 27 | |
Rat glenoid fossa | Maximum level of VEGF expression and new bone formation in the posterior region of the glenoid fossa during natural growth and forward mandibular positioning. Greatest amount of VEGF expression precedes the greatest increase in new bone formation | 36 | |
Rat glenoid fossa | Secretion of growth factors and cytokines by vascular endothelial cells was enhanced | 48 | |
Rabbit parietal bone defects | Combination of VEGF and DBMIM is a good graft material | 8 | |
Mouse tibia distraction osteogenesis | Both KDR and Flt-1 play important roles in neovascularisation and bone formation during distraction osteogenesis | 52 | |
In vitro | Distraction osteogenesis | Optimal angiogenic response and rate of distraction are closely related | 51 |
DBMIM, demineralized intramembranous bone matrix; Flt-1, vascular endothelial growth factor receptor-1; KDR, vascular endothelial growth factor receptor-2; VEGF, vascular endothelial growth factor.