Department of Dermatology, School of Medicine, University of California, San Francisco, San Francisco, CA, USA; Veteran Affairs Medical Center, San Francisco, CA, USA; Northern California Institute for Research and Education, San Francisco, CA, USA; Integrative Toxicology and Metabolism, Pôle de Toxicologie Alimentaire, Laboratoire de Pharmacologie et Toxicologie, Institut National de la Recherche Agronomique INRA UR66, Toulouse, France.
J Dermatol Sci. 2013 Dec;72(3):296-303. doi: 10.1016/j.jdermsci.2013.08.003. Epub 2013 Aug 23.
Ceramide hydrolysis by ceramidase in the stratum corneum (SC) yields both sphingoid bases and free fatty acids (FFA). While FFA are key constituents of the lamellar bilayers that mediate the epidermal permeability barrier, whether sphingoid bases influence permeability barrier homeostasis remains unknown. Pertinently, alterations of lipid profile, including ceramide and ceramidase activities occur in atopic dermatitis (AD).
We investigated alterations in sphingoid base levels and/or profiles (sphingosine to sphinganine ratio) in the SC of normal vs. AD mice, a model that faithfully replicates human AD, and then whether altered sphingoid base levels and/or profiles influence(s) membrane stability and/or structures.
Unilamellar vesicles (LV), incorporating the three major SC lipids (ceramides/FFA/cholesterol) and different ratios of sphingosine/sphinganine, encapsulating carboxyfluorescein, were used as the model of SC lipids. Membrane stability was measured as release of carboxyfluorescein. Thermal analysis of LV was conducted by differential scanning calorimetry (DSC).
LV containing AD levels of sphingosine/sphinganine (AD-LV) displayed altered membrane permeability vs. normal-LV. DSC analyses revealed decreases in orthorhombic structures that form tightly packed lamellar structures in AD-LV.
Sphingoid base composition influences lamellar membrane architecture in SC, suggesting that altered sphingoid base profiles could contribute to the barrier abnormality in AD.
角质层中的神经酰胺酶将神经酰胺水解为神经鞘氨醇碱基和游离脂肪酸(FFA)。虽然 FFA 是构成角质层细胞间脂质的重要成分,这些脂质有助于维持表皮渗透屏障的稳定性,但神经鞘氨醇碱基是否会影响渗透屏障的稳定性目前尚不清楚。值得注意的是,特应性皮炎(AD)患者的脂质谱发生改变,包括神经酰胺和神经酰胺酶的活性。
我们研究了正常和 AD 小鼠角质层中神经鞘氨醇碱基水平和/或谱(神经鞘氨醇/神经鞘氨醇碱基比值)的变化,AD 是一种能真实再现人类 AD 的模型,然后研究这些改变的神经鞘氨醇碱基水平和/或谱是否会影响膜的稳定性和/或结构。
我们使用包含三种主要角质层脂质(神经酰胺/FFA/胆固醇)和不同比例的神经鞘氨醇/神经鞘氨醇碱基的单分子层囊泡(LV)作为角质层脂质的模型,囊泡中包裹了羧基荧光素。通过释放羧基荧光素来测量膜的稳定性。通过差示扫描量热法(DSC)对 LV 的热分析进行了研究。
与正常-LV 相比,含有 AD 水平神经鞘氨醇/神经鞘氨醇碱基的 LV(AD-LV)显示出改变的膜通透性。DSC 分析显示 AD-LV 中形成紧密堆积的层状结构的正交结构减少。
神经鞘氨醇碱基的组成影响角质层中的层状膜结构,这表明改变的神经鞘氨醇碱基谱可能导致 AD 中的屏障异常。