Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Fujimoto, Tomokazu, Inoue, Toshihiro, Maki, Kei, Inoue-Mochita, Miyuki, Tanihara, Hidenobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
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
_version_ 1782451441412079616
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
work_keys_str_mv AT fujimototomokazu vascularendothelialgrowthfactoraincreasestheaqueoushumoroutflowfacility
AT inouetoshihiro vascularendothelialgrowthfactoraincreasestheaqueoushumoroutflowfacility
AT makikei vascularendothelialgrowthfactoraincreasestheaqueoushumoroutflowfacility
AT inouemochitamiyuki vascularendothelialgrowthfactoraincreasestheaqueoushumoroutflowfacility
AT taniharahidenobu vascularendothelialgrowthfactoraincreasestheaqueoushumoroutflowfacility