Tanaka Yohei, Parker Richard, Aganahi Amaryllis
Clinica Tanaka Plastic, Reconstructive Surgery and Anti-Aging Center, Matsumoto, Nagano, Japan.
RATIONALE, Kyneton, VIC, Australia.
Clin Cosmet Investig Dermatol. 2023 Oct 12;16:2829-2839. doi: 10.2147/CCID.S428170. eCollection 2023.
Clinical, optical and histological research confirms that solar skin damage continues to pose a threat to human skin health globally despite widespread sunscreen usage and sun awareness campaigns. Despite this, very few studies examine the critical changes in gene expression and DNA repair activity following recommended topical solar protection and repair strategies to ameliorate the harmful effects of ultraviolet, visible light and near-infrared radiation.
To investigate alterations in gene expression following topical solar protection and solar repair strategies.
Using epidermal keratinocytes and dermal fibroblasts derived from a 3-dimensional reconstructed human skin model, gene expression was assessed via the Genemarkers Standard Skin Panel using 112 genes deploying two analytical techniques: DNA microarray and quantitative real-time PCR exploration. Tissues were inoculated with products then collected after 24 hours following application of solar protection formulations and 16 hours following solar repair formulations (The Essential Six, RATIONALE, Victoria, Australia).
A DNA microarray revealed 67 genes that were significantly up-regulated or down-regulated following the treatment. The quantitative real-time PCR revealed that, in comparison to the control, the genes encoding Intercellular Adhesion Molecule 1 (ICAM1), Metallothionein 1A (MT1A), Prostaglandin-Endoperoxide Synthase 1 (PTGS2), Late Cornified Envelope 3D (LCE3D), Peroxisome Proliferator Activated Receptor (PPARD), and Granulocyte/Macrophage Colony Stimulating Factor 2 (GM-CSF2) have been up-regulated following usage of the solar protection regime, 1.87, 861.16, 4.34, 1.91, 1.06, and 3.6, respectively. ICAM1, MT1A, PTGS2, LCE3D, PPARD, and GM-CSF2 were up-regulated following use of the solar repair regime, 3.78, 2.98, 14.89, 5.09, 2.42, and 13.51, respectively.
This study demonstrates that a specific solar protection and repair regime upregulated genes involved in photoprotection and repair mechanisms in a 3-dimensional (3D) reconstructed human-like skin model.
临床、光学和组织学研究证实,尽管防晒霜广泛使用且开展了防晒宣传活动,但日光性皮肤损伤在全球范围内仍对人类皮肤健康构成威胁。尽管如此,很少有研究考察在采用推荐的局部防晒和修复策略以减轻紫外线、可见光和近红外辐射的有害影响后,基因表达和DNA修复活性的关键变化。
研究局部防晒和日光修复策略后基因表达的变化。
使用源自三维重建人体皮肤模型的表皮角质形成细胞和真皮成纤维细胞,通过Genemarkers标准皮肤面板,运用DNA微阵列和定量实时PCR探索这两种分析技术,对112个基因的表达进行评估。将产品接种到组织上,在涂抹防晒配方24小时后以及涂抹日光修复配方(澳大利亚维多利亚州RATIONALE公司的The Essential Six)16小时后收集样本。
DNA微阵列显示,处理后有67个基因显著上调或下调。定量实时PCR显示,与对照组相比,在使用防晒方案后,编码细胞间粘附分子1(ICAM1)、金属硫蛋白1A(MT1A)、前列腺素内过氧化物合酶1(PTGS2)、晚期角质化包膜3D(LCE3D)、过氧化物酶体增殖物激活受体(PPARD)和粒细胞/巨噬细胞集落刺激因子2(GM-CSF2)的基因分别上调了1.87、861.16、4.34、1.91、1.06和3.6倍。在使用日光修复方案后,ICAM1、MT1A、PTGS2、LCE3D、PPARD和GM-CSF2分别上调了3.78、2.98、14.89、5.09、2.42和13.51倍。
本研究表明,一种特定的防晒和修复方案可上调三维(3D)重建类人皮肤模型中参与光保护和修复机制的基因。