Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm
Özet
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/cm2 UVB exposure. At 24 J/cm2 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/cm2 UVA exhibited a 69.32% reduction in apoptotic processes compared to untreated cells. Similarly, when exposed to 100 mJ/cm2 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. © 2023 by the author.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Kuzucu, Mehmet | |
| dc.date.accessioned | 2026-10-18T20:26:38.363911885Z | |
| dc.date.available | 2026-10-18T20:26:38.363911885Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | 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/cm2 UVB exposure. At 24 J/cm2 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/cm2 UVA exhibited a 69.32% reduction in apoptotic processes compared to untreated cells. Similarly, when exposed to 100 mJ/cm2 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. © 2023 by the author. | |
| dc.identifier.doi | 10.3390/cimb45100528 | |
| dc.identifier.eissn | 1467-3045 | |
| dc.identifier.endpage | 8394 | |
| dc.identifier.issn | 1467-3037 | |
| dc.identifier.issue | 10 | |
| dc.identifier.pmcid | PMC10605247 | |
| dc.identifier.pmid | 37886971 | |
| dc.identifier.scopus | 2-s2.0-85175036461 | |
| dc.identifier.startpage | 8372 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/11613 | |
| dc.identifier.volume | 45 | |
| dc.identifier.wos | WOS:001098243100001 | |
| dc.language.iso | en | |
| dc.publisher | Multidisciplinary Digital Publishing Institute (MDPI) | |
| dc.relation.ispartof | Current Issues in Molecular Biology | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Deinococcus radiodurans | |
| dc.subject | deinoxanthin | |
| dc.subject | melanogenesis | |
| dc.subject | UV-induced damage | |
| dc.subject | ascorbic acid | |
| dc.subject | carotenoid | |
| dc.subject | superoxide dismutase | |
| dc.subject | xanthophyll | |
| dc.subject | zeaxanthin | |
| dc.subject | Article | |
| dc.subject | carbon nuclear magnetic resonance | |
| dc.subject | cell culture | |
| dc.subject | cell cycle progression | |
| dc.subject | cell growth | |
| dc.subject | cell migration | |
| dc.subject | cell proliferation | |
| dc.subject | cell viability | |
| dc.subject | chemical composition | |
| dc.subject | cytotoxicity test | |
| dc.subject | elemental analysis | |
| dc.subject | flow cytometry | |
| dc.subject | HFF-1 cell line | |
| dc.subject | human | |
| dc.subject | human cell | |
| dc.subject | hydrolysis | |
| dc.subject | IC50 | |
| dc.subject | immunohistochemistry | |
| dc.subject | lipid peroxidation | |
| dc.subject | MTT assay | |
| dc.subject | nonhuman | |
| dc.title | Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 11 | |
| rdl.citation.wos | 9 | |
| rdl.department | Department of Biology, Faculty of Arts and Sciences, Erzincan Binali Yildirim University, Erzincan 24100, Türkiye. | |
| rdl.oa.status | gold | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
