Lipides: systèmes analytiques et biologiques, Université Paris-Saclay, 92296, Châtenay-Malabry, France.
Analyst. 2021 Jul 21;146(14):4649-4658. doi: 10.1039/d1an00465d. Epub 2021 Jun 28.
Reconstructed human epidermis models are used as epidermis alternatives in skin research studies. It is necessary to provide molecular and functional characterization in order to assess these models. Our aim is to establish a link between the barrier function and the structure and composition of the stratum corneum using several complementary techniques. The following three studies were performed on reconstructed human epidermis during the keratinocyte differentiation process: (i) caffeine percutaneous penetration kinetics, (ii) epidermis thickness measurement, stratum corneum formation and lipid organization by Raman microspectroscopy and (iii) lipid composition evolution by liquid chromatography coupled to high-resolution mass spectrometry. The results demonstrated that the caffeine penetration decreased along the differentiation process. Raman in-depth images demonstrated an increase in stratum corneum and RHE thickness accompanied by the evolution of lipid organization. Lipid analysis showed an increase of the ceramide amount and an inverse relationship between ceramide and its precursor levels during the differentiation process. Different behaviors between several ceramide subclasses are highlighted and they relied on the corresponding differentiation stages. The generation of the most important ceramides for the barrier function is closely followed. A period shift between lipid generation and their organization was found. Our analytical data allowed identifying the following 3 groups of maturation days: before day 15, between days 15 and 19, and after day 19. The chemical and physiological states of the barrier function for each group are described thanks to a multimodal approach.
重建的人表皮模型被用作皮肤研究中表皮的替代品。为了评估这些模型,有必要对其进行分子和功能表征。我们的目的是使用几种互补的技术来建立屏障功能与角质层的结构和组成之间的联系。在角质形成细胞分化过程中,对重建的人表皮进行了以下三项研究:(i)咖啡因经皮渗透动力学,(ii)表皮厚度测量、通过拉曼微光谱学测量角质层形成和脂质组织以及(iii)通过液相色谱与高分辨率质谱联用测量脂质组成的演变。结果表明,咖啡因的渗透随着分化过程而降低。拉曼深度图像显示,随着脂质组织和 RHE 厚度的增加,其脂质组织也发生了变化。脂质分析表明,在分化过程中,神经酰胺的含量增加,而神经酰胺与其前体水平呈反比关系。强调了几种神经酰胺亚类之间的不同行为,并依赖于相应的分化阶段。密切关注了对屏障功能最重要的神经酰胺的生成。发现脂质生成与其组织之间存在时间上的转变。我们的分析数据允许确定以下 3 个成熟天数组:第 15 天之前、第 15 天至 19 天之间以及第 19 天之后。通过多模态方法描述了每个组的屏障功能的化学和生理状态。