Department I, Institute of Anatomy and Cell Biology, Ludwig-Maximilians-Universität München, Munich, Germany.
Institute of Applied Dermatopharmacy at the Martin Luther University Halle-Wittenberg (IADP), Halle/Saale, Germany,
Skin Pharmacol Physiol. 2020;33(4):213-230. doi: 10.1159/000509019. Epub 2020 Jul 17.
This review is the second part of a series which presents the state of the art in stratum corneum (SC) lipid matrix (LM) research in depth. In this part, the various hypothetical models which were developed to describe the structure and function of the SC LM as the skin's barrier will be discussed. New as well as a cumulative assortment of older results which change the view on the different models are considered to conclude how well the different models are holding up today. As a final conclusion, a model, factoring in as much of the known data as possible, is concluded, unifying the varying different models into one which can be developed further, as new results are found in the future. So far, the model is described with a single crystalline or gel-like phase with a certain amount of nanocrystallites of concentrated ceramides (CERs) and free fatty acids and more fluid nanodomains caused by a fluidizing effect of the cholesterol. These domains are dynamically resolved and reformed and do not impair the barrier function. The chain conformation is not completely clear yet; however, an equilibrium of fully extended and hairpin-folded CERs with ratios depending on the properties of each individual CER species is proposed as most likely. An overlapping middle layer as described for the tri-layer model in part I of this series would be present for both conformations. The macroscopic broad-narrow-broad layering, observed in electron micrographs, is explained by an external templating by the lipid envelope, and an internal templating by short and long lipid chains each preferentially show a homophilic association, forming thicker and thinner bilayers, respectively. The degree of influence of the very long ω-hydroxy-CERs is discussed as well.
这篇综述是系列文章的第二部分,深入介绍了角质层(SC)脂质基质(LM)研究的最新进展。在这一部分,将讨论各种假设模型,这些模型旨在描述 SC LM 的结构和功能,作为皮肤的屏障。新的以及累积的旧结果被认为可以改变对不同模型的看法,从而得出不同模型在今天的表现如何。作为最终结论,考虑到尽可能多的已知数据,得出了一个模型,将不同的模型统一为一个可以进一步发展的模型,因为未来会有新的结果。到目前为止,该模型被描述为具有单一结晶或凝胶相,其中含有一定量的浓缩神经酰胺(CER)纳米晶和游离脂肪酸,以及更多由胆固醇的流体化作用引起的流体纳米域。这些域是动态解析和重组的,不会损害屏障功能。链构象尚不完全清楚;然而,提出最有可能的情况是,CER 具有完全伸展和发夹折叠的平衡,其比率取决于每种 CER 物质的性质。与本系列第一部分中描述的三层模型一样,也会存在重叠的中层。在电子显微镜照片中观察到的宏观宽-窄-宽分层现象,通过脂质包膜的外部模板化和短链和长链脂质各自优先表现出同源缔合的内部模板化来解释,分别形成较厚和较薄的双层。还讨论了非常长的 ω-羟基-CER 的影响程度。