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Effects of Vitamin D(3) and Meso-Zeaxanthin on Human Retinal Pigmented Epithelial Cells in Three Integrated in vitro Paradigms of Age-Related Macular Degeneration
Age-related macular degeneration (AMD) is a degenerative retinal disease and one of major causes of irreversible vision loss. AMD has been linked to several pathological factors, such as oxidative stress and inflammation. Moreover, Aβ (1–42) oligomers have been found in drusen, the extracellular dep...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602342/ https://www.ncbi.nlm.nih.gov/pubmed/34803719 http://dx.doi.org/10.3389/fphar.2021.778165 |
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author | Lazzara, Francesca Conti, Federica Platania, Chiara Bianca Maria Eandi, Chiara M. Drago, Filippo Bucolo, Claudio |
author_facet | Lazzara, Francesca Conti, Federica Platania, Chiara Bianca Maria Eandi, Chiara M. Drago, Filippo Bucolo, Claudio |
author_sort | Lazzara, Francesca |
collection | PubMed |
description | Age-related macular degeneration (AMD) is a degenerative retinal disease and one of major causes of irreversible vision loss. AMD has been linked to several pathological factors, such as oxidative stress and inflammation. Moreover, Aβ (1–42) oligomers have been found in drusen, the extracellular deposits that accumulate beneath the retinal pigmented epithelium in AMD patients. Hereby, we investigated the hypothesis that treatment with 1,25(OH) (2)D(3) (vitamin D(3)) and meso-zeaxathin, physiologically present in the eye, would counteract the toxic effects of three different insults on immortalized human retinal pigmented epithelial cells (ARPE-19). Specifically, ARPE-19 cells have been challenged with Aβ (1–42) oligomers, H(2)O(2), LPS, and TNF-α, respectively. In the present study, we demonstrated that the combination of 1,25(OH)(2)D(3) and meso-zeaxanthin significantly counteracted the cell damage induced by the three insults, at least in these in vitro integrated paradigms of AMD. These results suggest that combination of 1,25(OH)(2)D(3) and meso-zeaxathin could be a useful approach to contrast pathological features of AMD, such as retinal inflammation and oxidative stress. |
format | Online Article Text |
id | pubmed-8602342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86023422021-11-20 Effects of Vitamin D(3) and Meso-Zeaxanthin on Human Retinal Pigmented Epithelial Cells in Three Integrated in vitro Paradigms of Age-Related Macular Degeneration Lazzara, Francesca Conti, Federica Platania, Chiara Bianca Maria Eandi, Chiara M. Drago, Filippo Bucolo, Claudio Front Pharmacol Pharmacology Age-related macular degeneration (AMD) is a degenerative retinal disease and one of major causes of irreversible vision loss. AMD has been linked to several pathological factors, such as oxidative stress and inflammation. Moreover, Aβ (1–42) oligomers have been found in drusen, the extracellular deposits that accumulate beneath the retinal pigmented epithelium in AMD patients. Hereby, we investigated the hypothesis that treatment with 1,25(OH) (2)D(3) (vitamin D(3)) and meso-zeaxathin, physiologically present in the eye, would counteract the toxic effects of three different insults on immortalized human retinal pigmented epithelial cells (ARPE-19). Specifically, ARPE-19 cells have been challenged with Aβ (1–42) oligomers, H(2)O(2), LPS, and TNF-α, respectively. In the present study, we demonstrated that the combination of 1,25(OH)(2)D(3) and meso-zeaxanthin significantly counteracted the cell damage induced by the three insults, at least in these in vitro integrated paradigms of AMD. These results suggest that combination of 1,25(OH)(2)D(3) and meso-zeaxathin could be a useful approach to contrast pathological features of AMD, such as retinal inflammation and oxidative stress. Frontiers Media S.A. 2021-11-05 /pmc/articles/PMC8602342/ /pubmed/34803719 http://dx.doi.org/10.3389/fphar.2021.778165 Text en Copyright © 2021 Lazzara, Conti, Platania, Eandi, Drago and Bucolo. https://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) and the copyright owner(s) 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 Lazzara, Francesca Conti, Federica Platania, Chiara Bianca Maria Eandi, Chiara M. Drago, Filippo Bucolo, Claudio Effects of Vitamin D(3) and Meso-Zeaxanthin on Human Retinal Pigmented Epithelial Cells in Three Integrated in vitro Paradigms of Age-Related Macular Degeneration |
title | Effects of Vitamin D(3) and Meso-Zeaxanthin on Human Retinal Pigmented Epithelial Cells in Three Integrated in vitro Paradigms of Age-Related Macular Degeneration |
title_full | Effects of Vitamin D(3) and Meso-Zeaxanthin on Human Retinal Pigmented Epithelial Cells in Three Integrated in vitro Paradigms of Age-Related Macular Degeneration |
title_fullStr | Effects of Vitamin D(3) and Meso-Zeaxanthin on Human Retinal Pigmented Epithelial Cells in Three Integrated in vitro Paradigms of Age-Related Macular Degeneration |
title_full_unstemmed | Effects of Vitamin D(3) and Meso-Zeaxanthin on Human Retinal Pigmented Epithelial Cells in Three Integrated in vitro Paradigms of Age-Related Macular Degeneration |
title_short | Effects of Vitamin D(3) and Meso-Zeaxanthin on Human Retinal Pigmented Epithelial Cells in Three Integrated in vitro Paradigms of Age-Related Macular Degeneration |
title_sort | effects of vitamin d(3) and meso-zeaxanthin on human retinal pigmented epithelial cells in three integrated in vitro paradigms of age-related macular degeneration |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602342/ https://www.ncbi.nlm.nih.gov/pubmed/34803719 http://dx.doi.org/10.3389/fphar.2021.778165 |
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