Literature DB >> 30971644

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

Daisuke Mikami1, Shota Sakai1,2, Kohei Yuyama1, Yasuyuki Igarashi1.   

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.

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Keywords:  Asterias amurensis; PPAR; keratinocyte; sphingoid d18:3; sphingolipid production

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Year:  2019        PMID: 30971644     DOI: 10.5650/jos.ess18256

Source DB:  PubMed          Journal:  J Oleo Sci        ISSN: 1345-8957            Impact factor:   1.601


  2 in total

1.  [Pathogenic and Compensatory Mechanisms in Epidermis of Sphingomyelin Synthase 2-Deficient Mice].

Authors:  Shota Sakai; Asami Makino; Akihito Nishi; Takeshi Ichikawa; Tadashi Yamashita; Makoto Taniguchi; Yoshihiro Tokudome; Yoshio Hirabayashi; Masashi Akiyama; Debra Crumrine; Yoshikazu Uchida; Peter M Elias; Tetsuya Tsuchida; Sumiko Hamanaka
Journal:  Skin Pharmacol Physiol       Date:  2021-04-29       Impact factor: 3.479

2.  Plant sphingolipids promote extracellular vesicle release and alleviate amyloid-β pathologies in a mouse model of Alzheimer's disease.

Authors:  Kohei Yuyama; Kaori Takahashi; Seigo Usuki; Daisuke Mikami; Hui Sun; Hisatoshi Hanamatsu; Junichi Furukawa; Katsuyuki Mukai; Yasuyuki Igarashi
Journal:  Sci Rep       Date:  2019-11-14       Impact factor: 4.379

  2 in total

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