July 2018
Volume 59, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2018
The Neuropilin-1 Interacting Region of VEGFA-165 Shifts the Acitvation of MAPK and AKT to a Pseudo-Binary Dose Response within Primary Human Retinal Endothelial Cells
Author Affiliations & Notes
  • Kenneth P Mitton
    Eye Research Institute, Oakland University, Rochester, Michigan, United States
  • Wendy A Dailey
    Eye Research Institute, Oakland University, Rochester, Michigan, United States
  • Austen Knapp
    Eye Research Institute & School of Medicine, Oakland University, Rochester, Michigan, United States
  • Peter Chen
    Eye Research Institute & School of Medicine, Oakland University, Rochester, Michigan, United States
  • Megan Moore
    Eye Research Institute, Oakland University, Rochester, Michigan, United States
  • Jennifer Felisky
    Eye Research Institute, Oakland University, Rochester, Michigan, United States
  • Anju Thomas
    Eye Research Institute, Oakland University, Rochester, Michigan, United States
  • Ed Guzman
    Eye Research Institute, Oakland University, Rochester, Michigan, United States
  • Mrinalini Deshpande
    Eye Research Institute, Oakland University, Rochester, Michigan, United States
  • Footnotes
    Commercial Relationships   Kenneth Mitton, None; Wendy Dailey, None; Austen Knapp, None; Peter Chen, None; Megan Moore, None; Jennifer Felisky, None; Anju Thomas, None; Ed Guzman, None; Mrinalini Deshpande, None
  • Footnotes
    Support  NIH Grant: EY025089 (Mitton). VRRF: (Mitton)
Investigative Ophthalmology & Visual Science July 2018, Vol.59, 4521. doi:
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      Kenneth P Mitton, Wendy A Dailey, Austen Knapp, Peter Chen, Megan Moore, Jennifer Felisky, Anju Thomas, Ed Guzman, Mrinalini Deshpande; The Neuropilin-1 Interacting Region of VEGFA-165 Shifts the Acitvation of MAPK and AKT to a Pseudo-Binary Dose Response within Primary Human Retinal Endothelial Cells. Invest. Ophthalmol. Vis. Sci. 2018;59(9):4521.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : VEGF is essential for retinal endothelial cell health, but elevated concentrations drive neo-vascular and inflammatory response in AMD, Diabetic Retinopathy, and ROP. Long-term consequences of anti-VEGF treatment is of concern as it reduces VEGF concentration to subnormal levels. Developing new treatments based on titrating VEGF concentration or modulating VEGF’s downstream effects is hindered by our lack of knowledge regarding VEGF's mechanisms within Human Retinal Endothelial Cells. Dose response curves of ligand-receptor binding cannot reveal activation kinetics; therefore, we developed in situ cellular assays to characterize the dose response curves for VEGFA-mediated activation at different points along intracellular signaling pathways.

Methods : Primary Human Microvascular Endothelial Cells (HRECs), from the same donor, were cultured using endothelial-specific media and techniques. Two isoforms of VEGFA-165 were utilized, one with an interaction site for the Neuropilin-1 coreceptor, and a b-isoform of VEGFA-165 that lacks the Neuropilin-1 interaction sequence. Dose responses were assayed using infra-red (IR) immunofluorescent labeling of activated MAPK, AKT and VEGFR2. For normalization, beta-Actin was co-labeled with a different IR tag. Dose response curves were fit using the DRC-package in the R-project statistical environment within OS-X.

Results : Activation of MAPK & AKT displayed a sharp pseudo-binary response to regular VEGFA-165 that contained the Neuropilin-1 interaction site. In contrast, activation responses were more gradual and less sensitive using an isoform of VEGFA-165 that lacked the Neuropilin-1 interaction sequence. ED50 values were 300-800 pM greater than for regular VEGFA-165. VEGFR2 activation displayed a similar large relative shift to sharper response.

Conclusions :
The C-terminus of VEGFA-165, which interacts with Neuropilin-1, dramatically decreases the ED50 values for the activation of both MAPK & AKT, creating a pseudo-binary response. This phenomenon was also seen for activation of VEGFR2. Our results reveal that it may be very difficult to titrate activation levels using the current VEGF blockade and traps. However, there may be room to reduce the high doses of anti-VEGF currently in use, now that we have determined the first dose response curves for Human Retinal Endothelial Cells.

This is an abstract that was submitted for the 2018 ARVO Annual Meeting, held in Honolulu, Hawaii, April 29 - May 3, 2018.

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