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Temporal requirement of RPE‐derived VEGF in the development of choroidal vasculature
Author(s) -
Le YunZheng,
Bai Yanyan,
Zhu Meili,
Zheng Lixin
Publication year - 2010
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2010.06573.x
Subject(s) - vascular endothelial growth factor , retinal , retina , electroretinography , biology , retinal pigment epithelium , conditional gene knockout , vascular endothelial growth factor a , immunohistochemistry , pathology , choroidal neovascularization , histology , anatomy , microbiology and biotechnology , vegf receptors , medicine , neuroscience , cancer research , phenotype , genetics , gene , biochemistry
J. Neurochem. (2010) 112 , 1584–1592. Abstract Vascular endothelial growth factor (VEGF‐A or VEGF) is a potent growth factor for the development of retinal and choroidal vasculatures. To define the temporal requirement of the retinal pigmented epithelium (RPE)‐derived VEGF in choroidal vascular development, we generated conditional VEGF knockout mice using an inducible Cre/ lox system. The loss of the RPE‐derived VEGF was confirmed with immunoblotting and immunohistochemistry. Retinal function and structure were assessed with electroretinography and histology, respectively. Choroidal vascular density was analyzed with computer‐assisted semi‐quantitative assay using fluorescently labeled choroidal flat‐mounts. Induction of RPE‐specific VEGF disruption at embryonic day 10 (E10) or E13 for 2 days caused regulatable decreases in choroidal vascular density, photoreceptor function, and photoreceptor outer nuclear layer thickness. The loss of the RPE‐produced VEGF after E15 did not cause detectable defects in choroidal vasculatures and photoreceptor function and morphology. These results suggest that the RPE‐derived VEGF plays a critical role in choroidal vascular development during organogenesis before E15.