June 2015
Volume 56, Issue 7
Free
ARVO Annual Meeting Abstract  |   June 2015
The Effect of VEGF-A on Trabecular Meshwork and Schlemm’s Canal Endothelial Cells Permeability
Author Affiliations & Notes
  • Tomokazu Fujimoto
    Department of Ophthalmology, Kumamoto University, Faculty of Life Sciences, Kumamoto, Japan
  • Toshihiro Inoue
    Department of Ophthalmology, Kumamoto University, Faculty of Life Sciences, Kumamoto, Japan
  • Kei Maki
    Department of Ophthalmology, Kumamoto University, Faculty of Life Sciences, Kumamoto, Japan
  • Sachi Kojima
    Department of Ophthalmology, Kumamoto University, Faculty of Life Sciences, Kumamoto, Japan
  • Miyuki Inoue-Mochita
    Department of Ophthalmology, Kumamoto University, Faculty of Life Sciences, Kumamoto, Japan
  • Hidenobu Tanihara
    Department of Ophthalmology, Kumamoto University, Faculty of Life Sciences, Kumamoto, Japan
  • Footnotes
    Commercial Relationships Tomokazu Fujimoto, None; Toshihiro Inoue, None; Kei Maki, None; Sachi Kojima, None; Miyuki Inoue-Mochita, None; Hidenobu Tanihara, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 2008. doi:
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      Tomokazu Fujimoto, Toshihiro Inoue, Kei Maki, Sachi Kojima, Miyuki Inoue-Mochita, Hidenobu Tanihara; The Effect of VEGF-A on Trabecular Meshwork and Schlemm’s Canal Endothelial Cells Permeability. Invest. Ophthalmol. Vis. Sci. 2015;56(7 ):2008.

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

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Abstract

Purpose: Anti-vascular endothelial growth factor (VEGF) antibody therapy is effective for ocular angiogenesis. Altough some patients increased their intraocular pressure after anti-VEGF therapy, the effects of VEGF agonists on aqueous humor outflow pathway remain unknown. The purpose of this study is to investige the VEGF-A effects on aqueous humor outflow pathway.

Methods: We used human recombinant VEGF165 and VEGF121 protein in this study. Trabecular meshwork (TM) cells and Schlemm’s canal endothelial (SCE) cells were isolated from the cynomolgus monkey eyes. The SCE and TM cells permeability was evaluated by measuring transendothelial electrical resistance (TEER).

Results: The TEER of SCE-cell was decreased by VEGF121 (30 nM) treated for 24 (71.8 ± 13.3 % compared to baseline, n=6) and 48 hours (62.8 ± 9.5 % compared to baseline, n=6). VEGF165 (30 nM) decreased the TEER of SCE-cell only 48 hours after treatment (65.4 ± 14.6 % compared to base line, n=6). On the other hand, the TEER of TM-cell was not affected by VEGF121 or VEGF165 treatment.

Conclusions: These results suggest that VEGF-A may regulate the conventional aqueous outflow.

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