VEGF-blocking therapy is used to treat neovascular proliferation and retinal edema in AMD and diabetic retinopathy. VEGF affects many processes, including: angiogenesis, vascular homeostasis, neovascularization, inflammatory response and disruption of the blood retinal barrier. Furthermore, several isoforms of VEGFA may drive either neovascularization or retinal edema (leaky blood vessels). VEGF-blocking drugs injected into the eye can enter the circulation and drop serum levels of VEGFA. Also, the safety of using VEGF-blockers for retinopathy of prematurity is unclear because treatment could block normal vessel growth. Thus, it is important to understand the mechanisms of VEGFA's action in the retina. Gaps remain in our knowledge because most investigations do not differentiate between the different isoforms of VEGFA. VEGFA-165 is an isoform that drives neovascular retinal disease. Recently, so-called anti- angiogenic b-isoforms of VEGFA were discovered including VEGFA-165b. There are suggestions that VEGFA-165b might be used therapeutically to counter retinal the neovascularization, but we don't know if VEGFA-165b causes vascular leakage like its regular isoform. We hypothesize that VEGFA-165b can still disrupt the blood retinal barrier and cause inflammation, regardless of its anti-angiogenic activity. In fact our preliminary data indicate this is so. To test this hypothesis, and with the involvement of numerous undergraduate students, we developed an intravitreal injection model (rat) to compare the effects of VEGFA-165 and -165b on the retinal vasculature. We will also use cultures of Human Retinal Endothelial Cells to compare the cell-signaling pathways activated by both isoforms in this cell-type. Results will increase our understanding of molecular events triggered by each VEGFA-165 isoform, and provide a model system with future application to study the efficacy and safely of new VEGF-modulating drugs.

Public Health Relevance

Increased Vascular Endothelial Growth Factor A-165 (VEGFA-165) concentration causes the growth of leaky new blood vessels in retinopathy of prematurity, diabetic retinopathy and Age-related Macular Degeneration. A related form called VEGFA-165b is considered a possible therapy to counter to VEGFA-165's growth effects. However, we hypothesize that VEGFA-165b still causes already formed vessels to leak like VEGFA-165, and we have developed a rat-based model and cell-culture model to confirm or disprove this hypothesis and answer this important question.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15EY025089-01A1
Application #
9022581
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Greenwell, Thomas
Project Start
2016-02-01
Project End
2019-01-31
Budget Start
2016-02-01
Budget End
2019-01-31
Support Year
1
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Oakland University
Department
Type
Organized Research Units
DUNS #
041808262
City
Rochester
State
MI
Country
United States
Zip Code
48309
Dailey, Wendy A; Drenser, Kimberly A; Wong, Sui Chien et al. (2017) Norrin treatment improves ganglion cell survival in an oxygen-induced retinopathy model of retinal ischemia. Exp Eye Res 164:129-138
Dailey, Wendy A; Drenser, Kimberly A; Wong, Sui Chien et al. (2017) Ocular coherence tomography image data of the retinal laminar structure in a mouse model of oxygen-induced retinopathy. Data Brief 15:491-495