Sanllehí Pol, Abad José-Luis, Casas Josefina, Delgado Antonio
Research Unit on Bioactive Molecules, Department of Biomedicinal Chemistry, Institute for Advanced Chemistry of Catalonia (IQAC-CSIC), Jordi Girona 18-26, E-08034 Barcelona, Spain; University of Barcelona (UB), Faculty of Pharmacy, Department of Pharmacology and Medicinal Chemistry, Unit of Pharmaceutical Chemistry (Associated Unit to CSIC), Avga. Joan XXIII s/n, E-08028 Barcelona, Spain.
Research Unit on Bioactive Molecules, Department of Biomedicinal Chemistry, Institute for Advanced Chemistry of Catalonia (IQAC-CSIC), Jordi Girona 18-26, E-08034 Barcelona, Spain.
Chem Phys Lipids. 2016 May;197:69-81. doi: 10.1016/j.chemphyslip.2015.07.007. Epub 2015 Jul 19.
Sphingolipids (SLs) are essential structural and signaling molecules of eukaryotic cells. Among them, sphingosine 1 phosphate (S1P) is a recognized promoter of cell survival, also involved, inter alia, in inflammation and tumorigenesis processes. The knowledge and modulation of the enzymes implicated in the biosynthesis and degradation of S1P are capital to control the intracellular levels of this lipid and, ultimately, to determine the cell fate. Starting with a general overview of the main metabolic pathways involved in SL metabolism, this review is mainly focused on the description of the most relevant findings concerning the development of modulators of S1P, namely inhibitors of the enzymes regulating S1P synthesis (sphingosine kinases) and degradation (sphingosine 1 phosphate phosphatase and lyase). In addition, a brief overview of the most significant agonists and antagonists at the S1P receptors is also addressed.
鞘脂(SLs)是真核细胞重要的结构和信号分子。其中,1-磷酸鞘氨醇(S1P)是公认的细胞存活促进因子,尤其还参与炎症和肿瘤发生过程。了解和调控参与S1P生物合成及降解的酶对于控制这种脂质的细胞内水平并最终决定细胞命运至关重要。本文首先对鞘脂代谢的主要代谢途径进行总体概述,主要聚焦于描述有关S1P调节剂开发的最相关研究结果,即调节S1P合成的酶(鞘氨醇激酶)和降解的酶(1-磷酸鞘氨醇磷酸酶和裂解酶)的抑制剂。此外,还简要概述了S1P受体最重要的激动剂和拮抗剂。