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Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm
This research delved into the protective capacities of deinoxanthin, a carotenoid present in Deinococcus radiodurans, against UVA- and UVB-mediated skin damage using human fibroblast foreskin cells (HFF-1). Using the MTT assay, HFF-1 cells treated with 10 µM DNX displayed 20% and 31.7% higher viabil...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605247/ https://www.ncbi.nlm.nih.gov/pubmed/37886971 http://dx.doi.org/10.3390/cimb45100528 |
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author | Kuzucu, Mehmet |
author_facet | Kuzucu, Mehmet |
author_sort | Kuzucu, Mehmet |
collection | PubMed |
description | This research delved into the protective capacities of deinoxanthin, a carotenoid present in Deinococcus radiodurans, against UVA- and UVB-mediated skin damage using human fibroblast foreskin cells (HFF-1). Using the MTT assay, HFF-1 cells treated with 10 µM DNX displayed 20% and 31.7% higher viability than the positive (Vitamin C-treated) and negative (DNX-untreated) control groups, respectively, upon 100 mJ/cm(2) UVB exposure. At 24 J/cm(2) UVA, 20 µM DNX-treated cells showed 80.6% viability, exceeding the positive and negative control groups by 28.6% and 33.6%, respectively. Flow cytometry analysis revealed that cells treated with DNX and exposed to 24 J/cm(2) UVA exhibited a 69.32% reduction in apoptotic processes compared to untreated cells. Similarly, when exposed to 100 mJ/cm(2) UVB, DNX-treated cells demonstrated a 72.35% decrease in apoptotic processes relative to their untreated counterparts. DNX also displayed dose-dependent inhibition on tyrosinase activity. The study emphasized DNX’s antioxidative capacity, evident in its modulation of superoxide dismutase activity and measurements of Malondialdehyde and intracellular reactive oxygen species levels. DNX-treated cells exhibited higher hydroxyproline levels, suggesting healthier collagen production. Additionally, the wound-healing assay method confirmed an accelerated healing rate in DNX-treated cells. Conclusively, DNX offers significant protection against UV-induced skin damage, emphasizing its potential for skincare and therapeutics. |
format | Online Article Text |
id | pubmed-10605247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106052472023-10-28 Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm Kuzucu, Mehmet Curr Issues Mol Biol Article This research delved into the protective capacities of deinoxanthin, a carotenoid present in Deinococcus radiodurans, against UVA- and UVB-mediated skin damage using human fibroblast foreskin cells (HFF-1). Using the MTT assay, HFF-1 cells treated with 10 µM DNX displayed 20% and 31.7% higher viability than the positive (Vitamin C-treated) and negative (DNX-untreated) control groups, respectively, upon 100 mJ/cm(2) UVB exposure. At 24 J/cm(2) UVA, 20 µM DNX-treated cells showed 80.6% viability, exceeding the positive and negative control groups by 28.6% and 33.6%, respectively. Flow cytometry analysis revealed that cells treated with DNX and exposed to 24 J/cm(2) UVA exhibited a 69.32% reduction in apoptotic processes compared to untreated cells. Similarly, when exposed to 100 mJ/cm(2) UVB, DNX-treated cells demonstrated a 72.35% decrease in apoptotic processes relative to their untreated counterparts. DNX also displayed dose-dependent inhibition on tyrosinase activity. The study emphasized DNX’s antioxidative capacity, evident in its modulation of superoxide dismutase activity and measurements of Malondialdehyde and intracellular reactive oxygen species levels. DNX-treated cells exhibited higher hydroxyproline levels, suggesting healthier collagen production. Additionally, the wound-healing assay method confirmed an accelerated healing rate in DNX-treated cells. Conclusively, DNX offers significant protection against UV-induced skin damage, emphasizing its potential for skincare and therapeutics. MDPI 2023-10-16 /pmc/articles/PMC10605247/ /pubmed/37886971 http://dx.doi.org/10.3390/cimb45100528 Text en © 2023 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kuzucu, Mehmet Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm |
title | Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm |
title_full | Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm |
title_fullStr | Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm |
title_full_unstemmed | Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm |
title_short | Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm |
title_sort | extremophilic solutions: the role of deinoxanthin in counteracting uv-induced skin harm |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605247/ https://www.ncbi.nlm.nih.gov/pubmed/37886971 http://dx.doi.org/10.3390/cimb45100528 |
work_keys_str_mv | AT kuzucumehmet extremophilicsolutionstheroleofdeinoxanthinincounteractinguvinducedskinharm |