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EP300 Protects from Light-Induced Retinopathy in Zebrafish

Exposure of rhodopsin to bright white light can induce photoreceptor cell damage and degeneration. However, a comprehensive understanding of the mechanisms underlying light-induced retinopathy remains elusive. In this study, we performed comparative transcriptome analysis of three rodent models of l...

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Autores principales: Kawase, Reiko, Nishimura, Yuhei, Ashikawa, Yoshifumi, Sasagawa, Shota, Murakami, Soichiro, Yuge, Mizuki, Okabe, Shiko, Kawaguchi, Koki, Yamamoto, Hiroshi, Moriyuki, Kazumi, Yamane, Shinsaku, Tsuruma, Kazuhiro, Shimazawa, Masamitsu, Hara, Hideaki, Tanaka, Toshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871856/
https://www.ncbi.nlm.nih.gov/pubmed/27242532
http://dx.doi.org/10.3389/fphar.2016.00126
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author Kawase, Reiko
Nishimura, Yuhei
Ashikawa, Yoshifumi
Sasagawa, Shota
Murakami, Soichiro
Yuge, Mizuki
Okabe, Shiko
Kawaguchi, Koki
Yamamoto, Hiroshi
Moriyuki, Kazumi
Yamane, Shinsaku
Tsuruma, Kazuhiro
Shimazawa, Masamitsu
Hara, Hideaki
Tanaka, Toshio
author_facet Kawase, Reiko
Nishimura, Yuhei
Ashikawa, Yoshifumi
Sasagawa, Shota
Murakami, Soichiro
Yuge, Mizuki
Okabe, Shiko
Kawaguchi, Koki
Yamamoto, Hiroshi
Moriyuki, Kazumi
Yamane, Shinsaku
Tsuruma, Kazuhiro
Shimazawa, Masamitsu
Hara, Hideaki
Tanaka, Toshio
author_sort Kawase, Reiko
collection PubMed
description Exposure of rhodopsin to bright white light can induce photoreceptor cell damage and degeneration. However, a comprehensive understanding of the mechanisms underlying light-induced retinopathy remains elusive. In this study, we performed comparative transcriptome analysis of three rodent models of light-induced retinopathy, and we identified 37 genes that are dysregulated in all three models. Gene ontology analysis revealed that this gene set is significantly associated with a cytokine signaling axis composed of signal transducer and activator of transcription 1 and 3 (STAT1/3), interleukin 6 signal transducer (IL6ST), and oncostatin M receptor (OSMR). Furthermore, the analysis suggested that the histone acetyltransferase EP300 may be a key upstream regulator of the STAT1/3–IL6ST/OSMR axis. To examine the role of EP300 directly, we developed a larval zebrafish model of light-induced retinopathy. Using this model, we demonstrated that pharmacological inhibition of EP300 significantly increased retinal cell apoptosis, decreased photoreceptor cell outer segments, and increased proliferation of putative Müller cells upon exposure to intense light. These results suggest that EP300 may protect photoreceptor cells from light-induced damage and that activation of EP300 may be a novel therapeutic approach for the treatment of retinal degenerative diseases.
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spelling pubmed-48718562016-05-30 EP300 Protects from Light-Induced Retinopathy in Zebrafish Kawase, Reiko Nishimura, Yuhei Ashikawa, Yoshifumi Sasagawa, Shota Murakami, Soichiro Yuge, Mizuki Okabe, Shiko Kawaguchi, Koki Yamamoto, Hiroshi Moriyuki, Kazumi Yamane, Shinsaku Tsuruma, Kazuhiro Shimazawa, Masamitsu Hara, Hideaki Tanaka, Toshio Front Pharmacol Pharmacology Exposure of rhodopsin to bright white light can induce photoreceptor cell damage and degeneration. However, a comprehensive understanding of the mechanisms underlying light-induced retinopathy remains elusive. In this study, we performed comparative transcriptome analysis of three rodent models of light-induced retinopathy, and we identified 37 genes that are dysregulated in all three models. Gene ontology analysis revealed that this gene set is significantly associated with a cytokine signaling axis composed of signal transducer and activator of transcription 1 and 3 (STAT1/3), interleukin 6 signal transducer (IL6ST), and oncostatin M receptor (OSMR). Furthermore, the analysis suggested that the histone acetyltransferase EP300 may be a key upstream regulator of the STAT1/3–IL6ST/OSMR axis. To examine the role of EP300 directly, we developed a larval zebrafish model of light-induced retinopathy. Using this model, we demonstrated that pharmacological inhibition of EP300 significantly increased retinal cell apoptosis, decreased photoreceptor cell outer segments, and increased proliferation of putative Müller cells upon exposure to intense light. These results suggest that EP300 may protect photoreceptor cells from light-induced damage and that activation of EP300 may be a novel therapeutic approach for the treatment of retinal degenerative diseases. Frontiers Media S.A. 2016-05-19 /pmc/articles/PMC4871856/ /pubmed/27242532 http://dx.doi.org/10.3389/fphar.2016.00126 Text en Copyright © 2016 Kawase, Nishimura, Ashikawa, Sasagawa, Murakami, Yuge, Okabe, Kawaguchi, Yamamoto, Moriyuki, Yamane, Tsuruma, Shimazawa, Hara and Tanaka. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Kawase, Reiko
Nishimura, Yuhei
Ashikawa, Yoshifumi
Sasagawa, Shota
Murakami, Soichiro
Yuge, Mizuki
Okabe, Shiko
Kawaguchi, Koki
Yamamoto, Hiroshi
Moriyuki, Kazumi
Yamane, Shinsaku
Tsuruma, Kazuhiro
Shimazawa, Masamitsu
Hara, Hideaki
Tanaka, Toshio
EP300 Protects from Light-Induced Retinopathy in Zebrafish
title EP300 Protects from Light-Induced Retinopathy in Zebrafish
title_full EP300 Protects from Light-Induced Retinopathy in Zebrafish
title_fullStr EP300 Protects from Light-Induced Retinopathy in Zebrafish
title_full_unstemmed EP300 Protects from Light-Induced Retinopathy in Zebrafish
title_short EP300 Protects from Light-Induced Retinopathy in Zebrafish
title_sort ep300 protects from light-induced retinopathy in zebrafish
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871856/
https://www.ncbi.nlm.nih.gov/pubmed/27242532
http://dx.doi.org/10.3389/fphar.2016.00126
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