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The inhibition of retinal neovascularization by gold nanoparticles via suppression of VEGFR-2 activation

Cited 111 time in Web of Science Cited 129 time in Scopus
Authors

Kim, Jin Hyoung; Kim, Myung Hun; Jo, Dong Hyun; Yu, Young Suk; Lee, Tae Geol; Kim, Jeong Hun

Issue Date
2011-03
Publisher
Pergamon Press Ltd.
Citation
Biomaterials, Vol.32 No.7, pp.1865-1871
Abstract
The pathological angiogenesis in the retina is the major cause of vision loss at all ages. In particular, retinopathy of prematurity CROP) is a leading cause of blindness in children. This study investigated whether gold nanoparticle (GNP) could inhibit retinal neovascularization in the animal model of ROP. Intravitreal injection of GNP significantly inhibited retinal neovascularization in the mouse model of ROP. In addition, GNP effectively suppressed VEGF-induced in vitro angiogenesis of retinal microvascular endothelial cells including proliferation, migration and capillary-like networks formation. GNP blocked VEGF-induced autophosphorylation of VEGFR-2 to inhibit consequently ERK 1/2 activation. GNP never affected on the cellular viability of retinal microvascular endothelial cells and induced no retinal toxicity. Our data suggest that GNP could be a potent inhibitor to retinal neovascularization without retinal toxicity. Furthermore, GNP could be extensively applied to variable vaso-proliferative retinopathies mediated by VEGF. (C) 2010 Elsevier Ltd. All rights reserved.
ISSN
0142-9612
URI
https://hdl.handle.net/10371/191649
DOI
https://doi.org/10.1016/j.biomaterials.2010.11.030
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