Objective: The effect of Zinc Finger Protein-Activating Transcription Factor ( ZFP-ATF) stimulating the angiogenesis and maturity of neovascularization with the overexpression of the vascular endothelial growth factor(VEGF )were investigated in a mouse ischemia hindlimb model and rat mesenteric assay;Methods: After the synthesis of ZFP-ATP, the ischemic hindlimb mice were successfully constructed. ZFP-ATF, VEGF165 and saline control were injected into the ischemic muscles, respectively. After 14 days, the number of mice with different ischemic degree was counted, moreover,the ischemic gastrocnemius and soleus muscle were harvested for the immunohistochemical staining and VEGF protein analysis.Besides, in the rat mesenteric assay, ZFP-ATF, VEGF165 and saline control were injected into mesenteric adipose tissues, respectively. After 14 days, the number of neovessels in different groups was calculated. Meanwhile, mesenteric immunofluorescence staining was performed to evaluate the pericyte coverage.Results: In the mouse with the ischemic hindlimb, the expression of VEGF protein in the ZFP-ATF group was significantly higher,at the same time, the number of neovessels in the ZFP-ATF evaluated by CD31 staining was significantly increased than that in the VEGF165 and blank control group. Besides, in the rat mesenteric assay, the number of neovessels in the ZFP-ATF group was dramatically increased compared with VEGF165 and blank group. In mesenteric immunofluorescence staining, the ZFP-ATF group had a more complete and successive pericytes coverage. Conclusion: ZFP-ATF stimulating the endogenous physiological angiogenesis can promote the more mature neovascularization with the complete pericyte coverage.