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Vascular Endothelial Growth Factor-A Increases the Aqueous Humor Outflow Facility
PURPOSE: Anti-vascular endothelial growth factor (VEGF) antibody therapy is an effective treatment for ocular angiogenesis. Although the intraocular pressure of some patients increases after anti-VEGF therapy, the effects of VEGF-A on the aqueous humor outflow pathway remain unknown. This study inve...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008796/ https://www.ncbi.nlm.nih.gov/pubmed/27584577 http://dx.doi.org/10.1371/journal.pone.0161332 |
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author | Fujimoto, Tomokazu Inoue, Toshihiro Maki, Kei Inoue-Mochita, Miyuki Tanihara, Hidenobu |
author_facet | Fujimoto, Tomokazu Inoue, Toshihiro Maki, Kei Inoue-Mochita, Miyuki Tanihara, Hidenobu |
author_sort | Fujimoto, Tomokazu |
collection | PubMed |
description | PURPOSE: Anti-vascular endothelial growth factor (VEGF) antibody therapy is an effective treatment for ocular angiogenesis. Although the intraocular pressure of some patients increases after anti-VEGF therapy, the effects of VEGF-A on the aqueous humor outflow pathway remain unknown. This study investigated the effects of VEGF-A on the aqueous humor outflow pathway. METHODS: We used human recombinant VEGF121 and VEGF165. Trabecular meshwork (TM) and Schlemm’s canal endothelial (SCE) cells were isolated from the eyes of cynomolgus monkeys. Expression of mRNA coding four VEGF receptors, VEGFR1 (FLT1), VEGFR2 (KDR), neuropilin-1, and neuropilin-2, was examined by RT-PCR. To evaluate the permeability of cell monolayers, we measured transendothelial electrical resistance (TEER). The outflow facility was measured in perfused porcine anterior segment organ cultures treated with 30 ng/mL VEGF121 for 48 h. RESULTS: Four VEGF-A-related receptor mRNAs were expressed in TM and SCE cells. The TEER of TM cells was not significantly affected by VEGF121 or VEGF165 treatment. In contrast, the TEER of SCE cells was significantly lower 48 h after treatment with 30 ng/mL VEGF121 to 69.4 ± 12.2% of baseline (n = 10), which was a significant difference compared with the control (P = 0.0001). VEGF165 (30 ng/mL) decreased the TEER of SCE cells at 48 h after treatment to 72.3 ± 14.1% compared with the baseline (n = 10), which was not a significant difference compared with the control (P = 0.0935). Ki8751, a selective VEGFR2 inhibitor, completely suppressed the effect of VEGF121 on SCE cell permeability, although ZM306416, a selective VEGFR1 inhibitor, did not affect the VEGF121-induced decrease in TEER. Perfusion with 30 ng/mL of VEGF121 for 48 h significantly increased the outflow facility compared with the control (47.8 ± 28.5%, n = 5, P = 0.013). CONCLUSIONS: These results suggest that VEGF-A may regulate the conventional aqueous outflow of SCE cells through VEGFR2. |
format | Online Article Text |
id | pubmed-5008796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50087962016-09-27 Vascular Endothelial Growth Factor-A Increases the Aqueous Humor Outflow Facility Fujimoto, Tomokazu Inoue, Toshihiro Maki, Kei Inoue-Mochita, Miyuki Tanihara, Hidenobu PLoS One Research Article PURPOSE: Anti-vascular endothelial growth factor (VEGF) antibody therapy is an effective treatment for ocular angiogenesis. Although the intraocular pressure of some patients increases after anti-VEGF therapy, the effects of VEGF-A on the aqueous humor outflow pathway remain unknown. This study investigated the effects of VEGF-A on the aqueous humor outflow pathway. METHODS: We used human recombinant VEGF121 and VEGF165. Trabecular meshwork (TM) and Schlemm’s canal endothelial (SCE) cells were isolated from the eyes of cynomolgus monkeys. Expression of mRNA coding four VEGF receptors, VEGFR1 (FLT1), VEGFR2 (KDR), neuropilin-1, and neuropilin-2, was examined by RT-PCR. To evaluate the permeability of cell monolayers, we measured transendothelial electrical resistance (TEER). The outflow facility was measured in perfused porcine anterior segment organ cultures treated with 30 ng/mL VEGF121 for 48 h. RESULTS: Four VEGF-A-related receptor mRNAs were expressed in TM and SCE cells. The TEER of TM cells was not significantly affected by VEGF121 or VEGF165 treatment. In contrast, the TEER of SCE cells was significantly lower 48 h after treatment with 30 ng/mL VEGF121 to 69.4 ± 12.2% of baseline (n = 10), which was a significant difference compared with the control (P = 0.0001). VEGF165 (30 ng/mL) decreased the TEER of SCE cells at 48 h after treatment to 72.3 ± 14.1% compared with the baseline (n = 10), which was not a significant difference compared with the control (P = 0.0935). Ki8751, a selective VEGFR2 inhibitor, completely suppressed the effect of VEGF121 on SCE cell permeability, although ZM306416, a selective VEGFR1 inhibitor, did not affect the VEGF121-induced decrease in TEER. Perfusion with 30 ng/mL of VEGF121 for 48 h significantly increased the outflow facility compared with the control (47.8 ± 28.5%, n = 5, P = 0.013). CONCLUSIONS: These results suggest that VEGF-A may regulate the conventional aqueous outflow of SCE cells through VEGFR2. Public Library of Science 2016-09-01 /pmc/articles/PMC5008796/ /pubmed/27584577 http://dx.doi.org/10.1371/journal.pone.0161332 Text en © 2016 Fujimoto et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Fujimoto, Tomokazu Inoue, Toshihiro Maki, Kei Inoue-Mochita, Miyuki Tanihara, Hidenobu Vascular Endothelial Growth Factor-A Increases the Aqueous Humor Outflow Facility |
title | Vascular Endothelial Growth Factor-A Increases the Aqueous Humor Outflow Facility |
title_full | Vascular Endothelial Growth Factor-A Increases the Aqueous Humor Outflow Facility |
title_fullStr | Vascular Endothelial Growth Factor-A Increases the Aqueous Humor Outflow Facility |
title_full_unstemmed | Vascular Endothelial Growth Factor-A Increases the Aqueous Humor Outflow Facility |
title_short | Vascular Endothelial Growth Factor-A Increases the Aqueous Humor Outflow Facility |
title_sort | vascular endothelial growth factor-a increases the aqueous humor outflow facility |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008796/ https://www.ncbi.nlm.nih.gov/pubmed/27584577 http://dx.doi.org/10.1371/journal.pone.0161332 |
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