Endogenous VEGF is required for visual function: Evidence for a survival role on Müller cells and photoreceptors

Magali Saint-Geniez, Arindel S Maharaj, Tony E. Walshe, Budd A. Tucker, Eiichi Sekiyama, Tomoki Kurihara, Diane C. Darland, Michael J. Young, Patricia A. D'Amore

Research output: Contribution to journalArticle

423 Citations (Scopus)

Abstract

Background: Vascular endothelial growth factor (VEGF) is well known for its role in normal and pathologic neovascularization. However, a growing body of evidence indicates that VEGF also acts on non-vascular cells, both developmentally as well as in the adult. In light of the widespread use of systemic and intraocular anti-VEGF therapies for the treatment of angiogenesis associated with tumor growth and wet macular degeneration, systematic investigation of the role of VEGF in the adult retina is critical. Methods and Findings: Using immunohistochemistry and Lac-Z reporter mouse lines, we report that VEGF is produced by various cells in the adult mouse retina and that VEGFR2, the primary signaling receptor, is also widely expressed, with strong expression by Müller cells and photoreceptors. Systemic neutralization of VEGF was accomplished in mice by adenoviral expression of sFlt1. After 14 days of VEGF neutralization, there was no effect on the inner and outer retina vasculature, but a significant increase in apoptosis of cells in the inner and outer nuclear layers. By four weeks, the increase in neural cell death was associated with reduced thickness of the inner and outer nuclear layers and a decline in retinal function as measured by electroretinograms. siRNA-based suppression of VEGF expression in a Müller cell line in vitro supports the existence of an autocrine role for VEGF in Müller cell survival. Similarly, the addition of exogenous VEGF to freshly isolated photoreceptor cells and outer-nuclear-layer explants demonstrated VEGF to be highly neuroprotective. Conclusions: These results indicate an important role for endogenous VEGF in the maintenance and function of adult retina neuronal cells and indicate that anti-VEGF therapies should be administered with caution.

Original languageEnglish (US)
Article numbere3554
JournalPLoS One
Volume3
Issue number11
DOIs
StatePublished - Nov 3 2008
Externally publishedYes

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Photoreceptor Cells
vascular endothelial growth factors
photoreceptors
Vascular Endothelial Growth Factor A
cells
retina
Retina
angiogenesis
neutralization
Wet Macular Degeneration
mice
neurons
Cells
Pathologic Neovascularization
electroretinography
therapeutics
Cell death
small interfering RNA
Small Interfering RNA
cell viability

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

Saint-Geniez, M., Maharaj, A. S., Walshe, T. E., Tucker, B. A., Sekiyama, E., Kurihara, T., ... D'Amore, P. A. (2008). Endogenous VEGF is required for visual function: Evidence for a survival role on Müller cells and photoreceptors. PLoS One, 3(11), [e3554]. https://doi.org/10.1371/journal.pone.0003554

Endogenous VEGF is required for visual function : Evidence for a survival role on Müller cells and photoreceptors. / Saint-Geniez, Magali; Maharaj, Arindel S; Walshe, Tony E.; Tucker, Budd A.; Sekiyama, Eiichi; Kurihara, Tomoki; Darland, Diane C.; Young, Michael J.; D'Amore, Patricia A.

In: PLoS One, Vol. 3, No. 11, e3554, 03.11.2008.

Research output: Contribution to journalArticle

Saint-Geniez, M, Maharaj, AS, Walshe, TE, Tucker, BA, Sekiyama, E, Kurihara, T, Darland, DC, Young, MJ & D'Amore, PA 2008, 'Endogenous VEGF is required for visual function: Evidence for a survival role on Müller cells and photoreceptors', PLoS One, vol. 3, no. 11, e3554. https://doi.org/10.1371/journal.pone.0003554
Saint-Geniez, Magali ; Maharaj, Arindel S ; Walshe, Tony E. ; Tucker, Budd A. ; Sekiyama, Eiichi ; Kurihara, Tomoki ; Darland, Diane C. ; Young, Michael J. ; D'Amore, Patricia A. / Endogenous VEGF is required for visual function : Evidence for a survival role on Müller cells and photoreceptors. In: PLoS One. 2008 ; Vol. 3, No. 11.
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