CD146 as a promising therapeutic target for retinal and choroidal neovascularization diseases

被引:1
|
作者
Bai Xue [1 ]
Ping Wang [2 ]
Wenzhen Yu [3 ]
Jing Feng [2 ]
Jie Li [4 ]
Rulian Zhao [1 ]
Zhenglin Yang [1 ,5 ]
Xiyun Yan [2 ,6 ,7 ]
Hongxia Duan [2 ]
机构
[1] Sichuan Provincial Key Laboratory for Human Disease Gene Study,Sichuan Provincial People's Hospital,School of Medicine,University of Electronic Science and Technology of China
[2] Key Laboratory of Protein and Peptide Pharmaceutical,Institute of Biophysics,Chinese Academy of Sciences
[3] Department of Ophthalmology,People's Hospital,Peking University
[4] Department of Ophthalmology,Sichuan Provincial People's Hospital,University of Electronic Science and Technology of China
[5] Research Unit for Blindness Prevention of Chinese Academy of Medical Sciences (2019RU026),Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital
[6] Nanozyme Medical Center,School of Basic Medical Sciences,Zhengzhou University
[7] College of Life Sciences,University of Chinese Academy of Sciences
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Blood vessel dysfunction causes several retinal diseases,including diabetic retinopathy,familial exudative vitreoretinopathy,macular degeneration and choroidal neovascularization in pathological myopia.Vascular endothelial growth factor(VEGF)-neutralizing proteins provide benefits in most of those diseases,yet unsolved haemorrhage and frequent intraocular injections still bothered patients.Here,we identified endothelial CD146 as a new target for retinal diseases.CD146 expression was activated in two ocular pathological angiogenesis models,a laser-induced choroid neovascularization model and an oxygeninduced retinopathy model.The absence of CD146 impaired hypoxia-induced cell migration and angiogenesis both in cell lines and animal model.Preventive or therapeutic treatment with anti-CD146 antibody AA98 significantly inhibited hypoxia-induced aberrant retinal angiogenesis in two retinal disease models.Mechanistically,under hypoxia condition,CD146 was involved in the activation of NFκB,Erk and Akt signalling pathways,which are partially independent of VEGF.Consistently,anti-CD146therapy combined with anti-VEGF therapy showed enhanced impairment effect of hypoxia-induced angiogenesis in vitro and in vivo.Given the critical role of abnormal angiogenesis in retinal and choroidal diseases,our results provide novel insights into combinatorial therapy for neovascular fundus diseases.
引用
收藏
页码:1157 / 1170
页数:14
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