从海星多棘海盘车糖基神经酰胺中分离鞘氨醇碱及其对培养角质形成细胞中鞘脂生成的影响。

Isolation of Sphingoid Bases from Starfish Asterias amurensis Glucosylceramides and Their Effects on Sphingolipid Production in Cultured Keratinocytes.

作者信息

Mikami Daisuke, Sakai Shota, Yuyama Kohei, Igarashi Yasuyuki

机构信息

Laboratory of Biomembrane and Biofunctional Chemistry, Frontier Research Center for Advanced Material and Life science, Hokkaido University.

Department of Biochemistry & Cell Biology, National Institute of Infectious Diseases.

出版信息

J Oleo Sci. 2019 May 1;68(5):427-441. doi: 10.5650/jos.ess18256. Epub 2019 Apr 9.

Abstract

Starfish Asterias amurensis produces sphingoid bases d18:3, 9-methyl-d18:3 (9Me-d18:3), and d22:2, which possess unique structural features. In this study, sphingoid bases prepared from A. amurensis glucosylceramides displayed unexpected elution behaviors from a general octadecyl silyl high-performance liquid chromatography (HPLC) column. For separation and isolation, sphingoid bases were fractionated by octadecyl silyl HPLC after N-acetylation, yielding d18:3, 9Me-d18:3, and two d22:2 isomers. To compare the biological activities of individual sphingoid bases, their effects on sphingolipid production in normal human keratinocytes were evaluated. Treatment with sphingoid bases increased the content of ceramides, glucosylceramides, and sphingomyelins in keratinocytes. Moreover, ceramides, which contain saturated ultra-long-chain fatty acids (C30-34), were significantly increased by treatment with d18:3, but not with other A. amurensis sphingoid bases. The mRNA level of the early differentiation marker keratin 10 was markedly decreased and sphingolipid synthesis-related genes were slightly increased in keratinocytes exposed to A. amurensis-derived d18:3, 9Me-d18:3, and d22:2 isomers. These results suggest that A. amurensis-derived sphingoid bases induce differentiation to varying degrees, sphingolipid production depends on their chemical structures, and d18:3 is the most promising functional sphingoid base.

摘要

海星多棘海盘车产生具有独特结构特征的鞘氨醇碱d18:3、9-甲基-d18:3(9Me-d18:3)和d22:2。在本研究中,从多棘海盘车葡萄糖神经酰胺制备的鞘氨醇碱在普通十八烷基硅烷高效液相色谱(HPLC)柱上显示出意外的洗脱行为。为了分离和纯化,鞘氨醇碱在N-乙酰化后通过十八烷基硅烷HPLC进行分馏,得到d18:3、9Me-d18:3和两种d22:2异构体。为了比较各个鞘氨醇碱的生物活性,评估了它们对正常人角质形成细胞中鞘脂产生的影响。用鞘氨醇碱处理增加了角质形成细胞中神经酰胺、葡萄糖神经酰胺和鞘磷脂的含量。此外,含有饱和超长链脂肪酸(C30-34)的神经酰胺在用d18:3处理后显著增加,但用其他多棘海盘车鞘氨醇碱处理则没有增加。在暴露于多棘海盘车来源的d18:3、9Me-d18:3和d22:2异构体的角质形成细胞中,早期分化标志物角蛋白10的mRNA水平显著降低,鞘脂合成相关基因略有增加。这些结果表明,多棘海盘车来源的鞘氨醇碱在不同程度上诱导分化,鞘脂产生取决于它们的化学结构,并且d18:3是最有前景的功能性鞘氨醇碱。

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