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Sphingosine 1-phosphate (S1P) is a sphingolipid derived from ceramide by an enzymatic reaction in vivo.1 S1P acts as a signaling molecule by binding to G-protein coupled receptors (S1PR) (S1P1-5 receptors) which results in activation of small GTPases such as Ras, Rac Rho and further downstream intracellular effects such as PI-3-Kinase, Protein kinase C and Hippo signaling pathways. This generates an effect on cell migration, differentiation and survival and therefore effects variety of systems such as immune system, central nervous system and cardiovascular system.2 For instance, S1P was found to inhibit cell apoptosis and induce cell proliferation by binding S1P1 to promote activation of ERK pathway.3 In addition, S1P was found to support cancer cells by inducing angiogenesis and survival of proliferative cells in the tumor microenvironment.4 Due to the vast activities of S1P and the resulted S1PR irregular activation, large discovery efforts are made to identify therapy by S1PR antagonists.
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文献和实验亦称4 -二氢(神经)鞘氨醇( sphingenin )。该物质在动物性鞘脂类中含量最多,是具有一个双键的 C 18 长链碱基。最初由 J.L.W.Thudichum ( 1961 )作为羟脑苷酯(半乳糖脑苷脂类的一种)的水解物获得。在某种酵母中呈游离型存在。也有微量以双链被还原的二羟基鞘氨醇和 C 16 及 C 20 的鞘氨醇形式存在。在植物、酵母、霉菌中,则以植物鞘氨醇( phytoaphingo-sine )为主,也可发现脱氢植物鞘氨醇、 C 20 植物鞘氨醇的存在
Sphingolipids (ceramide, sphingosine, and sphingosine-1-phosphate) are bioactive lipids with important biological functions in proliferation, apoptosis, angiogenesis, and inflammation. Herein, we describe easy and rapid biochemical methods
Sphingosine-1-phosphate (S1P) and the enzyme primarily responsible for its production, sphingosine kinase-1 (SphK-1), are thought to be dysregulated in multiple human diseases including cancer, multiple sclerosis (MS), diabetes, neurological
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