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Reactivating the extracellular matrix synthesis of sulfated glycosaminoglycans and proteoglycans to improve the human skin aspect and its mechanical properties

机译:重新激活硫酸化糖胺聚糖和蛋白聚糖的细胞外基质合成,以改善人体皮肤状况及其机械性能

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Background: The aim of this study was to demonstrate that a defined cosmetic composition is able to induce an increase in the production of sulfated glycosaminoglycans (sGAGs) and/or proteoglycans and finally to demonstrate that the composition, through its combined action of enzyme production and synthesis of macromolecules, modulates organization and skin surface aspect with a benefit in antiaging applications. Materials and methods: Gene expression was studied by quantitative reverse transcription polymerase chain reaction using normal human dermal fibroblasts isolated from a 45-year-old donor skin dermis. De novo synthesis of sGAGs and proteoglycans was determined using Blyscan? assay and/or immunohistochemical techniques. These studies were performed on normal human dermal fibroblasts (41- and 62-year-old donors) and on human skin explants. Dermis organization was studied either ex vivo on skin explants using bi-photon microscopy and transmission electron microscopy or directly in vivo on human volunteers by ultrasound technique. Skin surface modification was investigated in vivo using silicone replicas coupled with macrophotography, and the mechanical properties of the skin were studied using Cutometer. Results: It was first shown that mRNA expression of several genes involved in the synthesis pathway of sGAG was stimulated. An increase in the de novo synthesis of sGAGs was shown at the cellular level despite the age of cells, and this phenomenon was clearly related to the previously observed stimulation of mRNA expression of genes. An increase in the expression of the corresponding core protein of decorin, perlecan, and versican and a stimulation of their respective sGAGs, such as chondroitin sulfate and heparan sulfate, were found on skin explants. The biosynthesis of macromolecules seems to be correlated at the microscopic level to a better organization and quality of the dermis, with collagen fibrils having homogenous diameters. The dermis seems to be compacted as observed on images obtained by two-photon microscopy and ultrasound imaging. At the macroscopic level, this dermis organization shows a smoothed profile similar to a younger skin, with improved mechanical properties such as firmess. Conclusion: The obtained results demonstrate that the defined cosmetic composition induces the synthesis of sGAGs and proteoglycans, which contributes to the overall dermal reorganization. This activity in the dermis in turn impacts the surface and mechanical properties of the skin.
机译:背景:这项研究的目的是证明一种确定的化妆品组合物能够诱导硫酸化糖胺聚糖(sGAGs)和/或蛋白聚糖的产量增加,并最终证明该组合物通过其酶生产和水解的联合作用。合成大分子,调节组织和皮肤表面状况,在抗衰老应用中具有优势。材料和方法:使用从45岁供体皮肤真皮分离的正常人真皮成纤维细胞,通过定量逆转录聚合酶链反应研究了基因表达。使用Blyscan?确定sGAG和蛋白聚糖的从头合成。分析和/或免疫组化技术。这些研究是针对正常的人类真皮成纤维细胞(41岁和62岁的供体)和人类皮肤外植体进行的。使用双光子显微镜和透射电子显微镜在皮肤外植体上离体研究真皮组织,或者通过超声技术直接在人类志愿者体内对真皮组织进行研究。使用有机硅复制品和宏观摄影对体内皮肤表面修饰进行了研究,并使用Cutometer研究了皮肤的机械性能。结果:首次显示了sGAG合成途径中涉及的几个基因的mRNA表达被刺激。尽管细胞已老化,但在细胞水平上显示从头合成的sGAGs有所增加,这种现象显然与先前观察到的基因mRNA表达的刺激有关。在皮肤外植体上发现了decorin,perlecan和versican相应核心蛋白的表达增加,并刺激了它们各自的sGAG,例如硫酸软骨素和硫酸乙酰肝素。大分子的生物合成似乎在微观水平上与真皮的更好的组织和质量相关,胶原纤维具有均一的直径。如通过双光子显微镜和超声成像获得的图像所观察到的,真皮似乎被压实。在宏观层面上,该真皮组织显示出类似于年轻皮肤的平滑轮廓,并具有改善的机械特性,例如紧致度。结论:获得的结果表明,确定的化妆品成分可诱导sGAGs和蛋白聚糖的合成,从而有助于皮肤的整体重组。真皮中的这种活动继而影响皮肤的表面和机械性能。

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