Inhibition of retinal angiogenesis by gold nanoparticles via inducing autophagy

作     者：Ni Shen Rui Zhang Hao-Rui Zhang Hao-Yang Luo Wei Shen Xin Gao Da-Zhi Guo Jie Shen 

作者机构：Department of OphthalmologyShanghai Renji HospitalShanghai Jiao Tong University School of Medicine Department of OphthalmologyChanghai Hospitalthe Second Military Medical Univerisity Company 6 of Basic Medical Schoolthe Second Military Medical University School of Life ScienceFudan University Department of Hyperbaric OxygenNavy General Hospital 

出 版 物：《International Journal of Ophthalmology(English edition)》 (国际眼科杂志（英文版）)

年 卷 期：2018年第11卷第8期

页      面：1269-1276页

核心收录：

学科分类：0806[工学-冶金工程] 08[工学] 

基　　金：Supported by the National Natural Science Foundation of China (No.81401063) Shanghai Municipal Planning Commission of Science and Research Fund (No.201740054) Natural Science Foundation of Beijing (No.7153175) the Capital Health Research and Development of Special (No.2018-4-5111) Beijing Nova Program (No. Z16111000490000) Research Foundation for Youth of Second Military Medical University (No.2017QN13) Research Foundation for Youth of Changhai Hospital (No.CH201712 No.CH201820) 

主　　题：gold nanoparticles retinal angiogenesis oxygen induced retinopathy autophagy nanomedicine 

摘      要：AIM： To investigate the effect of gold nanoparticles on retinal angiogenesis in vitro and in vivo, and to reveal the possible ***： Seed growth method was used to synthesize gold nanoparticles（GNPs）. The size, zeta potential, absorption spectrum and morphology of GNPs were identified using Malvern Nano-ZS, multimode reader（Bio Tek synergy2） and transmission electron microscope. Cell viability was analyzed using cell counting kit-8 method and cell growth was assessed with EdU kit. Transwell chamber was used to investigate cell migration. Tube formation method was used to assess the angiogenic property in vitro. Oxygen induced retinopathy（OIR） model was used to investigate the effect of GNPs on retinal angiogenesis. Confocal microscope and Western blot were used to study the possible mechanism of GNPs inhibited ***： The GNPs synthesized were uniform and well dispersed. GNPs of 10 μg/mL and 20 μg/mL were able to inhibit human umbilical vein endothelial cells proliferation（50% and 72% separately, P〈0.001）, migration（54% and 83% separately, P〈0.001） and tube formation（52% and 90% separately, P〈0.001）. Further data showed that GNPs were able to improve the retinopathy in an OIR model. The possible mechanism might be that GNPs were able to induce autophagy significantly（P〈0.05）.CONCLUSION： The present study suggests that GNPs are able to inhibit retinal neovascularization in vitro and in vivo. GNPs might be a potential nanomedicine for the treatment of retinal angiogenesis.