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NFE2L2 activator RS9 protects against corneal epithelial cell damage in dry eye models
Oxidative stress may cause ocular surface damage during the development of dry eye. Mammalian cells have defense systems against oxidative stress. A central regulator of the stress response is nuclear factor-erythroid 2-related factor 2 (NFE2L2). NFE2L2 is activated by the novel triterpenoid RS9 (a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176120/ https://www.ncbi.nlm.nih.gov/pubmed/32320433 http://dx.doi.org/10.1371/journal.pone.0229421 |
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author | Matsuda, Yuka Machida, Mamiko Nakagami, Yasuhiro Nakajima, Takeshi Azuma, Mitsuyoshi |
author_facet | Matsuda, Yuka Machida, Mamiko Nakagami, Yasuhiro Nakajima, Takeshi Azuma, Mitsuyoshi |
author_sort | Matsuda, Yuka |
collection | PubMed |
description | Oxidative stress may cause ocular surface damage during the development of dry eye. Mammalian cells have defense systems against oxidative stress. A central regulator of the stress response is nuclear factor-erythroid 2-related factor 2 (NFE2L2). NFE2L2 is activated by the novel triterpenoid RS9 (a biotransformation compound of RTA 402). The purpose of this study was to assess the efficacy of RS9 against dry eye using in vitro and in vivo models. Bioactivity was estimated by the induction of mRNAs for two NFE2L2-targeted genes: NQO1 (prevents radical species) and GCLC (glutathione synthesis), using a corneal epithelial cell line (HCE-T). Protection against oxidation and cell damage was tested in vitro by culturing cells under hyperosmotic stress or by the addition of menadione, a generator of reactive oxygen species (ROS). Dry eye in vivo was induced by the injection of scopolamine into rats. Then, 930 nM of RS9 was applied to both eyes for 2 weeks. Oxidative stress was measured by the accumulation of 8-hydroxy-2’-deoxyguanosine (8-OHdG). Corneal wound healing was measured by scoring for superficial punctate keratitis (SPK). Corneal epithelial cell densities were evaluated histologically. RS9 and RTA 402 induced the expression of NQO1 and GCLC mRNAs in HCE-T cells. And both compounds suppressed hyperosmotic-ROS generation and menadione induced cellular damage. However RS9 had a stronger protective effect than RTA 402. Ocular instillation of RS9 also significantly upregulated the expression of Nqo1 mRNA in the corneal epithelium. Accumulation of 8-OHdG, increase of SPK scores and decrement of basal cell density were observed in corneal epithelium from scopolamine-injected rats. These changes were significantly ameliorated by the topical administration of RS9. RS9 induced Nfe2l2 activation and Nfe2l2-targeted genes, reduced oxidation, and ameliorated symptoms of dry eye using in vitro and in vivo models. Thus, RS9 might be a potent candidate agent against dry eye disease. |
format | Online Article Text |
id | pubmed-7176120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71761202020-05-12 NFE2L2 activator RS9 protects against corneal epithelial cell damage in dry eye models Matsuda, Yuka Machida, Mamiko Nakagami, Yasuhiro Nakajima, Takeshi Azuma, Mitsuyoshi PLoS One Research Article Oxidative stress may cause ocular surface damage during the development of dry eye. Mammalian cells have defense systems against oxidative stress. A central regulator of the stress response is nuclear factor-erythroid 2-related factor 2 (NFE2L2). NFE2L2 is activated by the novel triterpenoid RS9 (a biotransformation compound of RTA 402). The purpose of this study was to assess the efficacy of RS9 against dry eye using in vitro and in vivo models. Bioactivity was estimated by the induction of mRNAs for two NFE2L2-targeted genes: NQO1 (prevents radical species) and GCLC (glutathione synthesis), using a corneal epithelial cell line (HCE-T). Protection against oxidation and cell damage was tested in vitro by culturing cells under hyperosmotic stress or by the addition of menadione, a generator of reactive oxygen species (ROS). Dry eye in vivo was induced by the injection of scopolamine into rats. Then, 930 nM of RS9 was applied to both eyes for 2 weeks. Oxidative stress was measured by the accumulation of 8-hydroxy-2’-deoxyguanosine (8-OHdG). Corneal wound healing was measured by scoring for superficial punctate keratitis (SPK). Corneal epithelial cell densities were evaluated histologically. RS9 and RTA 402 induced the expression of NQO1 and GCLC mRNAs in HCE-T cells. And both compounds suppressed hyperosmotic-ROS generation and menadione induced cellular damage. However RS9 had a stronger protective effect than RTA 402. Ocular instillation of RS9 also significantly upregulated the expression of Nqo1 mRNA in the corneal epithelium. Accumulation of 8-OHdG, increase of SPK scores and decrement of basal cell density were observed in corneal epithelium from scopolamine-injected rats. These changes were significantly ameliorated by the topical administration of RS9. RS9 induced Nfe2l2 activation and Nfe2l2-targeted genes, reduced oxidation, and ameliorated symptoms of dry eye using in vitro and in vivo models. Thus, RS9 might be a potent candidate agent against dry eye disease. Public Library of Science 2020-04-22 /pmc/articles/PMC7176120/ /pubmed/32320433 http://dx.doi.org/10.1371/journal.pone.0229421 Text en © 2020 Matsuda 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 Matsuda, Yuka Machida, Mamiko Nakagami, Yasuhiro Nakajima, Takeshi Azuma, Mitsuyoshi NFE2L2 activator RS9 protects against corneal epithelial cell damage in dry eye models |
title | NFE2L2 activator RS9 protects against corneal epithelial cell damage in dry eye models |
title_full | NFE2L2 activator RS9 protects against corneal epithelial cell damage in dry eye models |
title_fullStr | NFE2L2 activator RS9 protects against corneal epithelial cell damage in dry eye models |
title_full_unstemmed | NFE2L2 activator RS9 protects against corneal epithelial cell damage in dry eye models |
title_short | NFE2L2 activator RS9 protects against corneal epithelial cell damage in dry eye models |
title_sort | nfe2l2 activator rs9 protects against corneal epithelial cell damage in dry eye models |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176120/ https://www.ncbi.nlm.nih.gov/pubmed/32320433 http://dx.doi.org/10.1371/journal.pone.0229421 |
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