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A novel AhR ligand, 2AI, protects the retina from environmental stress

Various retinal degenerative diseases including dry and neovascular age-related macular degeneration (AMD), retinitis pigmentosa, and diabetic retinopathy are associated with the degeneration of the retinal pigmented epithelial (RPE) layer of the retina. This consequently results in the death of rod...

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Autores principales: Gutierrez, Mark A., Davis, Sonnet S., Rosko, Andrew, Nguyen, Steven M., Mitchell, Kylie P., Mateen, Samiha, Neves, Joana, Garcia, Thelma Y., Mooney, Shaun, Perdew, Gary H., Hubbard, Troy D., Lamba, Deepak A., Ramanathan, Arvind
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929558/
https://www.ncbi.nlm.nih.gov/pubmed/27364765
http://dx.doi.org/10.1038/srep29025
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author Gutierrez, Mark A.
Davis, Sonnet S.
Rosko, Andrew
Nguyen, Steven M.
Mitchell, Kylie P.
Mateen, Samiha
Neves, Joana
Garcia, Thelma Y.
Mooney, Shaun
Perdew, Gary H.
Hubbard, Troy D.
Lamba, Deepak A.
Ramanathan, Arvind
author_facet Gutierrez, Mark A.
Davis, Sonnet S.
Rosko, Andrew
Nguyen, Steven M.
Mitchell, Kylie P.
Mateen, Samiha
Neves, Joana
Garcia, Thelma Y.
Mooney, Shaun
Perdew, Gary H.
Hubbard, Troy D.
Lamba, Deepak A.
Ramanathan, Arvind
author_sort Gutierrez, Mark A.
collection PubMed
description Various retinal degenerative diseases including dry and neovascular age-related macular degeneration (AMD), retinitis pigmentosa, and diabetic retinopathy are associated with the degeneration of the retinal pigmented epithelial (RPE) layer of the retina. This consequently results in the death of rod and cone photoreceptors that they support, structurally and functionally leading to legal or complete blindness. Therefore, developing therapeutic strategies to preserve cellular homeostasis in the RPE would be a favorable asset in the clinic. The aryl hydrocarbon receptor (AhR) is a conserved, environmental ligand-dependent, per ARNT-sim (PAS) domain containing bHLH transcription factor that mediates adaptive response to stress via its downstream transcriptional targets. Using in silico, in vitro and in vivo assays, we identified 2,2′-aminophenyl indole (2AI) as a potent synthetic ligand of AhR that protects RPE cells in vitro from lipid peroxidation cytotoxicity mediated by 4-hydroxynonenal (4HNE) as well as the retina in vivo from light-damage. Additionally, metabolic characterization of this molecule by LC-MS suggests that 2AI alters the lipid metabolism of RPE cells, enhancing the intracellular levels of palmitoleic acid. Finally, we show that, as a downstream effector of 2AI-mediated AhR activation, palmitoleic acid protects RPE cells from 4HNE-mediated stress, and light mediated retinal degeneration in mice.
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spelling pubmed-49295582016-07-06 A novel AhR ligand, 2AI, protects the retina from environmental stress Gutierrez, Mark A. Davis, Sonnet S. Rosko, Andrew Nguyen, Steven M. Mitchell, Kylie P. Mateen, Samiha Neves, Joana Garcia, Thelma Y. Mooney, Shaun Perdew, Gary H. Hubbard, Troy D. Lamba, Deepak A. Ramanathan, Arvind Sci Rep Article Various retinal degenerative diseases including dry and neovascular age-related macular degeneration (AMD), retinitis pigmentosa, and diabetic retinopathy are associated with the degeneration of the retinal pigmented epithelial (RPE) layer of the retina. This consequently results in the death of rod and cone photoreceptors that they support, structurally and functionally leading to legal or complete blindness. Therefore, developing therapeutic strategies to preserve cellular homeostasis in the RPE would be a favorable asset in the clinic. The aryl hydrocarbon receptor (AhR) is a conserved, environmental ligand-dependent, per ARNT-sim (PAS) domain containing bHLH transcription factor that mediates adaptive response to stress via its downstream transcriptional targets. Using in silico, in vitro and in vivo assays, we identified 2,2′-aminophenyl indole (2AI) as a potent synthetic ligand of AhR that protects RPE cells in vitro from lipid peroxidation cytotoxicity mediated by 4-hydroxynonenal (4HNE) as well as the retina in vivo from light-damage. Additionally, metabolic characterization of this molecule by LC-MS suggests that 2AI alters the lipid metabolism of RPE cells, enhancing the intracellular levels of palmitoleic acid. Finally, we show that, as a downstream effector of 2AI-mediated AhR activation, palmitoleic acid protects RPE cells from 4HNE-mediated stress, and light mediated retinal degeneration in mice. Nature Publishing Group 2016-07-01 /pmc/articles/PMC4929558/ /pubmed/27364765 http://dx.doi.org/10.1038/srep29025 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Gutierrez, Mark A.
Davis, Sonnet S.
Rosko, Andrew
Nguyen, Steven M.
Mitchell, Kylie P.
Mateen, Samiha
Neves, Joana
Garcia, Thelma Y.
Mooney, Shaun
Perdew, Gary H.
Hubbard, Troy D.
Lamba, Deepak A.
Ramanathan, Arvind
A novel AhR ligand, 2AI, protects the retina from environmental stress
title A novel AhR ligand, 2AI, protects the retina from environmental stress
title_full A novel AhR ligand, 2AI, protects the retina from environmental stress
title_fullStr A novel AhR ligand, 2AI, protects the retina from environmental stress
title_full_unstemmed A novel AhR ligand, 2AI, protects the retina from environmental stress
title_short A novel AhR ligand, 2AI, protects the retina from environmental stress
title_sort novel ahr ligand, 2ai, protects the retina from environmental stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929558/
https://www.ncbi.nlm.nih.gov/pubmed/27364765
http://dx.doi.org/10.1038/srep29025
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