Biological Materials Laboratory, CSIR-Central Leather Research Institute, Chennai, India.
Academy of Scientific and Innovative Research, CSIR-CLRI, Chennai, India.
J Cell Physiol. 2019 Aug;234(8):13110-13127. doi: 10.1002/jcp.27981. Epub 2018 Dec 17.
The redox state of the endothelial cells plays a key role in the regulation of the angiogenic process. The modulation of the redox state of endothelial cells (ECs) could be a viable target to alter angiogenic response. In the present work, we synthesized a redox modulator by caging 5-hydroxy 2-methyl 1, 4-napthoquinone (Plumbagin) on silver nano framework (PCSN) for tunable reactive oxygen species (ROS) inductive property and tested its role in ECs during angiogenic response in physiological and stimulated conditions. In physiological conditions, the redox modulators induced the angiogenic response by establishing ECs cell-cell contact in tube formation model, chorio allontoic membrane, and aortic ring model. The molecular mechanism of angiogenic response was induced by vascular endothelial growth factor receptor 2 (VEGFR2)/p42-mitogen-activated protein kinase signaling pathway. Under stimulation, by mimicking tumor angiogenic conditions it induced cytotoxicity by generation of excessive ROS and inhibited the angiogenic response by the loss of spatiotemporal regulation of matrix metalloproteases, which prevents the tubular network formation in ECs and poly-ADP ribose modification of VEGF. The mechanism of opposing effects of PCSN was due to modulation of PKM2 enzyme activity, which increased the EC sensitivity to ROS and inhibited EC survival in stimulated condition. In normal conditions, the endogenous reactive states of NOX4 enzyme helped the EC survival. The results indicated that a threshold ROS level exists in ECs that promote angiogenesis and any significant enhancement in its level by redox modulator inhibits angiogenesis. The study provides the cues for the development of redox-based therapeutic molecules to cure the disease-associated aberrant angiogenesis.
内皮细胞的氧化还原状态在调节血管生成过程中起着关键作用。调节内皮细胞 (EC) 的氧化还原状态可能是改变血管生成反应的可行靶点。在本工作中,我们通过将 5-羟基-2-甲基-1,4-萘醌(Plumbagin)笼封在银纳米框架 (PCSN) 上来合成一种氧化还原调节剂,以实现对活性氧 (ROS) 诱导特性的可调控制,并在生理和刺激条件下测试其在 EC 中对血管生成反应的作用。在生理条件下,氧化还原调节剂通过在管形成模型、绒毛尿囊膜和主动脉环模型中建立 EC 细胞-细胞接触来诱导血管生成反应。血管内皮生长因子受体 2 (VEGFR2)/p42-丝裂原活化蛋白激酶信号通路诱导血管生成反应的分子机制。在刺激下,通过模拟肿瘤血管生成条件,它通过产生过多的 ROS 诱导细胞毒性,并通过基质金属蛋白酶时空调节的丧失抑制血管生成反应,从而阻止 EC 中管状网络的形成和 VEGF 的聚 ADP 核糖修饰。PCSN 产生相反效果的机制是由于 PKM2 酶活性的调节,这增加了 EC 对 ROS 的敏感性,并抑制了刺激条件下 EC 的存活。在正常情况下,NOX4 酶的内源性反应状态有助于 EC 的存活。结果表明,EC 中存在促进血管生成的 ROS 阈值水平,任何通过氧化还原调节剂显著增强其水平都会抑制血管生成。该研究为开发基于氧化还原的治疗分子以治疗与疾病相关的异常血管生成提供了线索。