Animal models of choroidal and retinal neovascularization

被引:320
作者
Grossniklaus, Hans E. [1 ,2 ]
Kang, Shin J. [1 ]
Berglin, Lennart [3 ]
机构
[1] Emory Univ, Dept Ophthalmol, Atlanta, GA 30322 USA
[2] Emory Univ, Dept Pathol, Atlanta, GA 30322 USA
[3] St Eriks Eye Hosp, Karolinska Inst, Stockholm, Sweden
关键词
Choroidal neovascularization; Retinal neovascularization; Animal models; ENDOTHELIAL GROWTH-FACTOR; OXYGEN-INDUCED RETINOPATHY; EXPERIMENTAL PRERETINAL NEOVASCULARIZATION; PHOTODYNAMIC VENOUS THROMBOSIS; PIGMENT EPITHELIAL-CELLS; MACULAR DEGENERATION; SUBRETINAL NEOVASCULARIZATION; DIABETIC-RETINOPATHY; BRUCHS MEMBRANE; MOUSE MODEL;
D O I
10.1016/j.preteyeres.2010.05.003
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
There have been numerous types of animal models of choroidal neovascularization (CNV) and retinal neovascularization (RNV). Understanding the pathobiology of CNV and RNV is important when evaluating and utilizing these models. Both CNV and RNV are dynamic processes. A break or defect in Bruchs' membrane is necessary for CNV to develop. This may be induced with a laser, mechanically via surgery, or in the setting of transgenic mice. Some of the transgenic mouse models spontaneously develop RNV and/or retinal angiomatous proliferation (RAP)-like lesions. The pathogenesis of RNV is well-known and is generally related to ischemic retinopathy. Models of oxygen-induced retinopathy (OIR) closely resemble retinopathy of prematurity (ROP). The streptozotocin (STZ) rat model develops features similar to diabetic retinopathy. This review summarizes general categories and specific examples of animal models of CNV and RNV. There are no perfect models of CNV or RNV and individual investigators are encouraged to choose the model that best suits their needs. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:500 / 519
页数:20
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