Institute of Precision Medicine, Medical and Life Sciences Faculty, Furtwangen University, Jakob-Kienzle-Str. 17, D-78054 Villingen-Schwenningen, Germany.
Organic Chemistry, Martin-Luther University Halle-Wittenberg, Kurt-Mothes, Str. 2, D-06120 Halle (Saale), Germany.
Int J Mol Sci. 2024 Aug 28;25(17):9344. doi: 10.3390/ijms25179344.
Atopic dermatitis (AD) is a common inflammatory skin disease, in particular among infants, and is characterized, among other things, by a modification in fatty acid and ceramide composition of the skin's stratum corneum. Palmitic acid and stearic acid, along with C-ceramide and 2-hydroxy C-ceramide, occur strikingly in AD. They coincide with a simultaneous decrease in very long-chain ceramides and ultra-long-chain ceramides, which form the outermost lipid barrier. Ceramides originate from cellular sphingolipid/ceramide metabolism, comprising a well-orchestrated network of enzymes involving various ELOVLs and CerSs in the de novo ceramide synthesis and neutral and acid CERase in degradation. Contrasting changes in long-chain ceramides and very long-chain ceramides in AD can be more clearly explained by the compartmentalization of ceramide synthesis. According to our hypothesis, the origin of increased C-ceramide and 2-hydroxy C-ceramide is located in the lysosome. Conversely, the decreased ultra-long-chain and very long-chain ceramides are the result of impaired ELOVL fatty acid elongation. The suggested model's key elements include the lysosomal aCERase, which has pH-dependent long-chain C-ceramide synthase activity (revaCERase); the NADPH-activated step-in enzyme ELOVL6 for fatty acid elongation; and the coincidence of impaired ELOVL fatty acid elongation and an elevated lysosomal pH, which is considered to be the trigger for the altered ceramide biosynthesis in the lysosome. To maintain the ELOVL6 fatty acid elongation and the supply of NADPH and ATP to the cell, the polyunsaturated PPARG activator linoleic acid is considered to be one of the most suitable compounds. In the event that the increase in lysosomal pH is triggered by lysosomotropic compounds, compounds that disrupt the transmembrane proton gradient or force the breakdown of lysosomal proton pumps, non-HLA-classified AGEP may result.
特应性皮炎(AD)是一种常见的炎症性皮肤病,尤其是在婴儿中,其特征是皮肤角质层的脂肪酸和神经酰胺组成发生改变。棕榈酸和硬脂酸以及 C-神经酰胺和 2-羟基 C-神经酰胺在 AD 中明显存在。它们与极长链神经酰胺和超长链神经酰胺的同时减少相吻合,这些物质构成了最外层的脂质屏障。神经酰胺来源于细胞鞘脂/神经酰胺代谢,其中包括涉及从头合成神经酰胺的各种 ELOVL 和 CerSs 以及降解中的中性和酸性 CERase 的协调良好的酶网络。AD 中长链神经酰胺和极长链神经酰胺的对比变化可以通过神经酰胺合成的隔室化得到更清楚的解释。根据我们的假设,C-神经酰胺和 2-羟基 C-神经酰胺增加的来源位于溶酶体中。相反,超长链和极长链神经酰胺的减少是由于 ELOVL 脂肪酸延长受损所致。建议模型的关键要素包括溶酶体 aCERase,其具有 pH 依赖性长链 C-神经酰胺合酶活性(revaCERase);NADPH 激活的脂肪酸延伸步骤酶 ELOVL6;以及受损的 ELOVL 脂肪酸延伸和升高的溶酶体 pH 的巧合,这被认为是溶酶体中改变的神经酰胺生物合成的触发因素。为了维持 ELOVL6 脂肪酸延伸以及向细胞供应 NADPH 和 ATP,多不饱和的 PPARG 激活剂亚油酸被认为是最合适的化合物之一。如果溶酶体 pH 的增加是由溶酶体趋化性化合物触发的,则可能导致非 HLA 分类的 AGEP,这些化合物会破坏跨膜质子梯度或迫使溶酶体质子泵分解。