Potential role of sirtuin 1 in Müller glial cells in mice choroidal neovascularization.

This study investigated the potential role of sirtuin 1 in Müller glial cells in choroidal neovascularization. In the in vitro study, primary Müller glial cells were cultured and treated with resveratrol, a sirtuin 1 activator. Glial fibrillary acidic protein expression and angiogenesis-related gene...

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Main Authors: Tomoka Ishida, Takeshi Yoshida, Kosei Shinohara, Kejia Cao, Ken-Ichi Nakahama, Ikuo Morita, Kyoko Ohno-Matsui
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0183775&type=printable
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author Tomoka Ishida
Takeshi Yoshida
Kosei Shinohara
Kejia Cao
Ken-Ichi Nakahama
Ikuo Morita
Kyoko Ohno-Matsui
author_facet Tomoka Ishida
Takeshi Yoshida
Kosei Shinohara
Kejia Cao
Ken-Ichi Nakahama
Ikuo Morita
Kyoko Ohno-Matsui
author_sort Tomoka Ishida
collection DOAJ
description This study investigated the potential role of sirtuin 1 in Müller glial cells in choroidal neovascularization. In the in vitro study, primary Müller glial cells were cultured and treated with resveratrol, a sirtuin 1 activator. Glial fibrillary acidic protein expression and angiogenesis-related gene expression were examined using quantitative polymerase chain reaction and phagocytosis, as a marker of Müller glial cell function; in addition, a latex bead assay was used to analyze cell function. For the in vivo study, choroidal neovascularization was induced in C57BL/6 mice via laser photocoagulation, and resveratrol was administered intravitreally. Eyecup whole mounts were created to measure choroidal neovascularization volumes on day 7. Immunohistochemical analysis with anti-glial fibrillary acidic protein antibody was used to detect Müller glial cell activation in eyes with choroidal neovascularization on day 1, 3, 5, and 7 after laser surgery. Resveratrol significantly promoted glial fibrillary acidic protein, anti-angiogenic factor, pigment epithelium-derived factor, and thrombospondin-1 expression in the cells as well as the phagocytic activities. Treatment of the choroidal neovascularization model with resveratrol resulted in early activation of Müller glial cells near choroidal neovascularization sites. Resveratrol-activated cells but not the controls migrated to the top of choroidal neovascularization sites and into the lesions from day 3. Resveratrol reduced the choroidal neovascularization size relative to controls. In conclusion, sirtuin 1 activation in Müller glial cells suppressed the development of choroidal neovascularization, and therefore, might be a therapeutic option.
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spelling doaj-art-eada528a0f804b61af0b2d276e054d4c2025-08-20T03:04:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01129e018377510.1371/journal.pone.0183775Potential role of sirtuin 1 in Müller glial cells in mice choroidal neovascularization.Tomoka IshidaTakeshi YoshidaKosei ShinoharaKejia CaoKen-Ichi NakahamaIkuo MoritaKyoko Ohno-MatsuiThis study investigated the potential role of sirtuin 1 in Müller glial cells in choroidal neovascularization. In the in vitro study, primary Müller glial cells were cultured and treated with resveratrol, a sirtuin 1 activator. Glial fibrillary acidic protein expression and angiogenesis-related gene expression were examined using quantitative polymerase chain reaction and phagocytosis, as a marker of Müller glial cell function; in addition, a latex bead assay was used to analyze cell function. For the in vivo study, choroidal neovascularization was induced in C57BL/6 mice via laser photocoagulation, and resveratrol was administered intravitreally. Eyecup whole mounts were created to measure choroidal neovascularization volumes on day 7. Immunohistochemical analysis with anti-glial fibrillary acidic protein antibody was used to detect Müller glial cell activation in eyes with choroidal neovascularization on day 1, 3, 5, and 7 after laser surgery. Resveratrol significantly promoted glial fibrillary acidic protein, anti-angiogenic factor, pigment epithelium-derived factor, and thrombospondin-1 expression in the cells as well as the phagocytic activities. Treatment of the choroidal neovascularization model with resveratrol resulted in early activation of Müller glial cells near choroidal neovascularization sites. Resveratrol-activated cells but not the controls migrated to the top of choroidal neovascularization sites and into the lesions from day 3. Resveratrol reduced the choroidal neovascularization size relative to controls. In conclusion, sirtuin 1 activation in Müller glial cells suppressed the development of choroidal neovascularization, and therefore, might be a therapeutic option.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0183775&type=printable
spellingShingle Tomoka Ishida
Takeshi Yoshida
Kosei Shinohara
Kejia Cao
Ken-Ichi Nakahama
Ikuo Morita
Kyoko Ohno-Matsui
Potential role of sirtuin 1 in Müller glial cells in mice choroidal neovascularization.
PLoS ONE
title Potential role of sirtuin 1 in Müller glial cells in mice choroidal neovascularization.
title_full Potential role of sirtuin 1 in Müller glial cells in mice choroidal neovascularization.
title_fullStr Potential role of sirtuin 1 in Müller glial cells in mice choroidal neovascularization.
title_full_unstemmed Potential role of sirtuin 1 in Müller glial cells in mice choroidal neovascularization.
title_short Potential role of sirtuin 1 in Müller glial cells in mice choroidal neovascularization.
title_sort potential role of sirtuin 1 in muller glial cells in mice choroidal neovascularization
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0183775&type=printable
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