論文

査読有り 国際誌
2018年

Pharmacological Modulation of Glycosphingolipid Metabolism.

Methods in molecular biology (Clifton, N.J.)
  • Jin-Ichi Inokuchi
  • ,
  • Takashi Ode
  • ,
  • Miki Hara-Yokoyama

1804
開始ページ
401
終了ページ
410
記述言語
英語
掲載種別
DOI
10.1007/978-1-4939-8552-4_19

The experimental approach to deplete cellular glycosphingolipids (GSLs) with the specific inhibitors of glycosphingolipid biosynthesis has the potential to identify functions of endogenous GSLs. Most GSLs are derived from glucosylceramide (GlcCer). D-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP) inhibits GIcCer synthase and has been used extensively to study the biological functions of living cells. D-PDMP inhibits mTORC1 activity, which is independent of its inhibitory activity on GlcCer synthase. We also developed an analog of D-PDMP, D-threo-1-phenyl-2-benzyloxycarbonylamino-3-pyrrolidino-1-propanol (D-PBPP) lacking the effect on mTORC1. Here, we summarize the effects of D-PDMP and D-PBPP on the metabolism of GSLs and cell growth.

リンク情報
DOI
https://doi.org/10.1007/978-1-4939-8552-4_19
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/29926420
ID情報
  • DOI : 10.1007/978-1-4939-8552-4_19
  • PubMed ID : 29926420

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