Department of Dermatology, Medical University of Vienna, Austria; Christian Doppler Laboratory for the Biotechnology of Skin Aging, Vienna, Austria.
Department of Dermatology, Medical University of Vienna, Austria; Christian Doppler Laboratory for the Biotechnology of Skin Aging, Vienna, Austria.
Free Radic Biol Med. 2019 Nov 20;144:256-265. doi: 10.1016/j.freeradbiomed.2019.04.019. Epub 2019 Apr 18.
Dermatological research is a major beneficiary of the rapidly developing advances in lipid analytic technology and of bioinformatic tools which help to decipher and interpret the accumulating big lipid data. At its interface with the environment, the epidermis develops a blend of lipids that constitutes the epidermal lipid barrier, essential for the protection from water loss and entry of dangerous noxae. Apart from their structural role in the barrier, novel intra- and inter-cellular signaling functions of lipids and their oxidation products have been uncovered in most cutaneous cell types over the last decades, and the discovery rate has been boosted by the advent of high resolution and -throughput mass spectrometric techniques. Our understanding of epidermal development has benefited from studies on fetal surface lipids, which appear to signal for adaptation to desiccation post partum, and from studies on the dynamics of epidermal lipids during adjustment to the atmosphere in the first months of life. At birth, external insults begin to challenge the skin and its lipids, and recent years have yielded ample insights into the dynamics of lipid synthesis and -oxdiation after UV exposure, and upon contact with sensitizers and irritants. Psoriasis and atopic dermatitis are the most common chronic inflammatory skin diseases, affecting at least 3% and 7% of the global population, respectively. Consequently, novel (redox-) lipidomic techniques have been applied to study systemic and topical lipid abnormalities in patient cohorts. These studies have refined the knowledge on eicosanoid signaling in both diseases, and have identified novel biomarkers and potential disease mediators, such as lipid antigens recognized by psoriatic T cells, as well as ceramide species, which specifically correlate with atopic dermatitis severity. Both biomarkers have yielded novel mechanistic insights. Finally, the technological progress has enabled studies to be performed that have monitored the consequences of diet, lifestyle, therapy and cosmetic intervention on the skin lipidome, highlighting the translational potential of (redox-) lipidomics in dermatology.
皮肤科学研究是脂质分析技术和生物信息学工具快速发展的主要受益者,这些工具有助于解读和解释不断积累的大量脂质数据。在与环境的接触界面上,表皮会形成一层混合脂质,构成表皮脂质屏障,对于防止水分流失和有害物质进入至关重要。除了在屏障中发挥结构作用外,过去几十年中,在大多数皮肤细胞类型中发现了脂质及其氧化产物的新型细胞内和细胞间信号传递功能,而高分辨率和高通量质谱技术的出现则提高了发现速度。我们对表皮发育的理解得益于对胎儿表面脂质的研究,这些脂质似乎在出生后对干燥环境的适应发出信号,也得益于对表皮脂质在生命头几个月适应大气环境的动态变化的研究。出生时,外部刺激开始挑战皮肤及其脂质,近年来,人们对紫外线暴露后、接触敏化剂和刺激物后脂质合成和氧化的动态变化有了充分的了解。银屑病和特应性皮炎是最常见的慢性炎症性皮肤病,分别影响全球至少 3%和 7%的人口。因此,新型(氧化还原)脂质组学技术已被应用于研究患者队列中的系统性和局部性脂质异常。这些研究完善了这两种疾病中花生四烯酸信号转导的知识,并确定了新型生物标志物和潜在的疾病介质,如银屑病 T 细胞识别的脂质抗原,以及与特应性皮炎严重程度特异性相关的神经酰胺。这两种生物标志物都提供了新的机制见解。最后,技术进步使得能够监测饮食、生活方式、治疗和化妆品干预对皮肤脂质组的影响,突出了(氧化还原)脂质组学在皮肤科学中的转化潜力。