Moyle Christina W A, Cerezo Ana B, Winterbone Mark S, Hollands Wendy J, Alexeev Yuri, Needs Paul W, Kroon Paul A
Institute of Food Research, Norwich Research Park, Norwich, UK.
Mol Nutr Food Res. 2015 Mar;59(3):401-12. doi: 10.1002/mnfr.201400478. Epub 2015 Jan 22.
Excessive concentrations of vascular endothelial growth factor (VEGF) drive angiogenesis and cause complications such as increased growth of tumours and atherosclerotic plaques. The aim of this study was to determine the molecular mechanism underlying the potent inhibition of VEGF signalling by polyphenols.
We show that the polyphenols epigallocatechin gallate from green tea and procyanidin oligomers from apples potently inhibit VEGF-induced VEGF receptor-2 (VEGFR-2) signalling in human umbilical vein endothelial cells by directly interacting with VEGF. The polyphenol-induced inhibition of VEGF-induced VEGFR-2 activation occurred at nanomolar polyphenol concentrations and followed bi-phasic inhibition kinetics. VEGF activity could not be recovered by dialysing VEGF-polyphenol complexes. Exposure of VEGF to epigallocatechin gallate or procyanidin oligomers strongly inhibited subsequent binding of VEGF to human umbilical vein endothelial cells expressing VEGFR-2. Remarkably, even though VEGFR-2 signalling was completely inhibited at 1 μM concentrations of polyphenols, endothelial nitric oxide synthase was shown to still be activated via the PI3K/Akt signalling pathway which is downstream of VEGFR-2.
These data demonstrate for the first time that VEGF is a key molecular target for specific polyphenols found in tea, apples and cocoa which potently inhibit VEGF signalling and angiogenesis at physiological concentrations. These data provide a plausible mechanism which links bioactive compounds in food with their beneficial effects.
血管内皮生长因子(VEGF)浓度过高会驱动血管生成,并引发诸如肿瘤生长加快和动脉粥样硬化斑块等并发症。本研究的目的是确定多酚有效抑制VEGF信号传导的分子机制。
我们发现,绿茶中的表没食子儿茶素没食子酸酯和苹果中的原花青素低聚物通过与VEGF直接相互作用,有效抑制人脐静脉内皮细胞中VEGF诱导的VEGF受体2(VEGFR-2)信号传导。多酚诱导的对VEGF诱导的VEGFR-2激活的抑制作用在纳摩尔浓度的多酚下发生,并遵循双相抑制动力学。通过透析VEGF-多酚复合物无法恢复VEGF活性。将VEGF暴露于表没食子儿茶素没食子酸酯或原花青素低聚物会强烈抑制VEGF随后与人脐静脉内皮细胞中表达的VEGFR-2的结合。值得注意的是,尽管在1μM浓度的多酚下VEGFR-2信号传导被完全抑制,但内皮型一氧化氮合酶仍通过VEGFR-2下游的PI3K/Akt信号通路被激活。
这些数据首次证明,VEGF是茶、苹果和可可中发现的特定多酚的关键分子靶点,这些多酚在生理浓度下能有效抑制VEGF信号传导和血管生成。这些数据提供了一种合理的机制,将食物中的生物活性化合物与其有益作用联系起来。