A VEGF₁₆₅-induced phenotypic switch from increased vessel density to increased vessel diameter and increased endothelial NOS activity

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• 作者：Patricia Parsons-Wingerter ; Unni M. Ch ; rasekharan ; Terri L. McKay ; Krishnan Radhakrishnan ; Paul E. DiCorleto ; Brian Albarran ; Andrew G. Farr
• 关键词：VEGF ; Angiogenesis ; Fractal ; Nitric oxide ; NOS ; Chorioallantoic membrane ; CAM ; Quail ; Avian
• 刊名：Microvascular Research
• 出版年：2006
• 出版时间：November 2006
• 年：2006
• 卷：72
• 期：3
• 页码：91-100
• 全文大小：605 K

文摘

Although vascular endothelial growth factor-165 (VEGF₁₆₅) regulates numerous angiogenic cellular activities, its complex effects on vascular morphology are not highly quantified. By fractal-based, multiparametric branching analysis of 2D vascular pattern in the quail chorioallantoic membrane (CAM), we report that vessel density increased maximally at lower VEGF concentrations, but that vessel diameter and activity of endothelial nitric oxide synthase (eNOS) increased maximally at higher VEGF concentrations. Following exogenous application of human VEGF₁₆₅ to the CAM at embryonic day 7, vessel density and diameter were measured after 24 h at arterial end points by the fractal dimension (D_f) and generational branching parameters for vessel area density (A_v), vessel length density (L_v) and vessel diameter (D_v) using the computer code VESGEN. The VEGF-dependent phenotypic switch from normal vessels displaying increased vessel density to abnormal, dilated vessels typical of tumor vasculature and other pathologies resulted from an approximate threefold increase in VEGF concentration (1.25 to 5 μg/CAM) and correlated positively with increased eNOS activity. Relative to control specimens, eNOS activity increased maximally to 60 % following VEGF treatment at 5 μg/CAM, compared to 10 % at 1.25 μg/CAM, and was accompanied by no significant change in activity of inducible NOS. In summary, VEGF₁₆₅ induced a phenotypic switch from increased vessel density associated with low VEGF concentration, to increased vessel diameter and increased eNOS activity at high VEGF concentration.