[HTML][HTML] Vascular endothelial growth factor as an autocrine survival factor for retinal pigment epithelial cells under oxidative stress via the VEGF-R2/PI3K/Akt

SH Byeon, SC Lee, SH Choi, HK Lee… - … & visual science, 2010 - iovs.arvojournals.org
SH Byeon, SC Lee, SH Choi, HK Lee, JH Lee, YK Chu, OW Kwon
Investigative ophthalmology & visual science, 2010iovs.arvojournals.org
Purpose.: Vascular endothelial cell growth factor (VEGF) is strongly induced by oxidative
stress in retinal pigment epithelial (RPE) cells, and VEGF-A is a survival factor for various
cell types. This study was conducted to determine whether the autocrine VEGF signaling
pathway in RPE cells is involved in the mechanism of adaptive response to oxidative stress.
Methods.: ARPE-19 cells were treated with hydrogen peroxide, and cell death was
measured by flow cytometry with annexin V-fluorescein isothiocyanate. Survival analysis …
Abstract
Purpose.: Vascular endothelial cell growth factor (VEGF) is strongly induced by oxidative stress in retinal pigment epithelial (RPE) cells, and VEGF-A is a survival factor for various cell types. This study was conducted to determine whether the autocrine VEGF signaling pathway in RPE cells is involved in the mechanism of adaptive response to oxidative stress.
Methods.: ARPE-19 cells were treated with hydrogen peroxide, and cell death was measured by flow cytometry with annexin V-fluorescein isothiocyanate. Survival analysis was performed with pretreatment of VEGF-A–neutralizing antibodies, VEGF receptor tyrosine kinase inhibitor (SU5416), or VEGF-A receptor-neutralizing antibodies (anti-VEGF-R1 and anti-VEGF-R2). The expression of VEGF-A,-R1,-R2, and soluble VEGF-R1 was determined by semiquantitative RT-PCR or Western blot analysis. Phosphorylation of VEGF-R2 was detected with immunoprecipitation and immunoblot analysis.
Results.: Hydrogen peroxide–induced cell death was promoted by pretreatment with VEGF-A and anti-VEGF-R2–neutralizing antibodies, but not with anti-VEGF-R1–neutralizing antibody. Phosphorylation of VEGF-R2 in RPE cells was induced by hydrogen peroxide, and pretreatment with anti-VEGF-A–neutralizing antibody inhibited phosphorylation. Phosphorylation of Akt under oxidative stress was abrogated by pretreatment with neutralizing antibodies against either VEGF-A or SU5416.
Conclusions.: Autocrine VEGF-A enhanced RPE cell survival under oxidative stress; the autocrine VEGF-A/VEGF-R2/PI3K/Akt pathway is involved. Neutralization of VEGF-A signaling, as in eyes with age-related macular degeneration, may influence RPE cell survival.
ARVO Journals