Skin Physiology Laboratory, School of Bioscience and Biotechnology, Tokyo University of Technology, Tokyo, Japan.
Department of Food Science and Nutrition, and Convergence Program of Material Science for Medicine and Pharmaceutics, Hallym University, Chuncheon, Republic of Korea.
Skin Pharmacol Physiol. 2023;36(3):149-159. doi: 10.1159/000529743. Epub 2023 Mar 16.
The outermost layer of the skin, the epidermis, is directly exposed to external stress (e.g., irradiation, allergens, and chemicals). Changes in epidermal conditions/environment in response to this stress could also influence conditions of the dermis, located directly beneath the epidermis. Yet, whether/how any epidermal environment changes in response to external stress affect dermal functions has not been completely clarified.
We employed ultraviolet irradiation B (UVB) (which hardly reaches the dermis) as a model of external stress. Human keratinocytes and human dermal fibroblasts were treated with UVB and conditioned medium of keratinocytes exposed to UVB (UVB-keratinocyte-M), respectively. We assessed (1) inflammatory cytokines and lipid mediators in keratinocytes; (2) matrix metalloprotease (MMP) levels and collagen degradation in fibroblasts; (3) ex vivo organ-cultured human skin was treated with UVB. MMP levels and collagen degradation were examined; (4) test whether the mixture of agent (agent cocktail) consisting of dihydroceramide, niacin amide, resveratrol, glucosyl hesperidin, and phytosterol ester that has been shown to improve skin barrier integrity can mitigate influence of UVB in skin; and (5) a pilot one-arm human clinical test to assess efficacy of formulation containing agent cocktail on stratum corneum hydration, skin elasticity, and wrinkle index.
Inflammatory-cytokine and -lipid mediator production were increased in cultured keratinocytes treated with UVB, while matrix MMP-1, -3, and -9 production and collagen degradation were increased in fibroblasts incubated with UVB-keratinocyte-M. mRNA expression of COL1A1 (that codes type 1 collagen) levels was decreased in fibroblasts incubated with UVB-keratinocyte-M. The study using ex vivo organ-cultured human skin showed both MMP-1 and MMP-9 expression were increased in both epidermis and dermis and increased dermal collagen degradation following UVB irradiation. Increased MMP production and collagen degradation were attenuated by application of an agent cocktail. Finally, a pilot clinical study demonstrated that the formulation containing our agent cocktail likely has the ability to improve skin hydration, increase skin elasticity, and reduce the appearance of wrinkles.
Epidermal changes in epidermal environment and conditions in response to external stress affect dermal conditions, and these negative effects of external stress on various skin layers can be pharmacologically mitigated.
皮肤的最外层表皮直接暴露于外部应激(如辐射、过敏原和化学物质)之下。表皮对这些应激的条件/环境变化也可能影响位于表皮下方的真皮的状况。然而,表皮对外部应激的任何环境变化如何影响真皮功能尚未完全阐明。
我们采用紫外线 B(UVB)照射(几乎不能到达真皮)作为外部应激的模型。用 UVB 分别处理人角质形成细胞和人真皮成纤维细胞,以及用 UVB 处理过的角质形成细胞的条件培养基(UVB-角质形成细胞-M)。我们评估了(1)角质形成细胞中的炎症细胞因子和脂质介质;(2)成纤维细胞中的基质金属蛋白酶(MMP)水平和胶原降解;(3)用 UVB 处理离体器官培养的人皮肤,检查 MMP 水平和胶原降解;(4)测试已显示可改善皮肤屏障完整性的二氢神经酰胺、烟酰胺、白藜芦醇、葡萄糖基橙皮苷和植物甾醇酯组成的混合剂(试剂鸡尾酒)是否可以减轻 UVB 对皮肤的影响;以及(5)一项初步的单臂人体临床测试,以评估含有试剂鸡尾酒的配方对角质层含水量、皮肤弹性和皱纹指数的疗效。
用 UVB 处理的培养角质形成细胞中炎症细胞因子和脂质介质的产生增加,而用 UVB-角质形成细胞-M 孵育的成纤维细胞中 MMP-1、-3 和 -9 的产生和胶原降解增加。用 UVB-角质形成细胞-M 孵育的成纤维细胞中 COL1A1(编码 1 型胶原)的 mRNA 表达水平降低。使用离体器官培养的人皮肤的研究表明,UVB 照射后,表皮和真皮中 MMP-1 和 MMP-9 的表达均增加,真皮胶原降解增加。应用试剂鸡尾酒可减轻 MMP 产生和胶原降解的增加。最后,一项初步的临床研究表明,含有我们试剂鸡尾酒的配方可能具有改善皮肤水分、增加皮肤弹性和减少皱纹外观的能力。
表皮对环境变化和条件的反应会影响真皮状况,外部应激对各皮肤层的这些负面影响可以通过药理学手段减轻。