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鞘氨醇-1-磷酸:G蛋白偶联受体EDG-1家族的一种配体。

Sphingosine 1-phosphate: a ligand for the EDG-1 family of G-protein-coupled receptors.

作者信息

Spiegel S

机构信息

Department of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, DC 20007, USA.

出版信息

Ann N Y Acad Sci. 2000 Apr;905:54-60. doi: 10.1111/j.1749-6632.2000.tb06537.x.

DOI:10.1111/j.1749-6632.2000.tb06537.x
PMID:10818441
Abstract

Ample evidence indicates that sphingosine-1-phosphate (SPP) can serve as an intracellular second messenger regulating calcium mobilization, cell growth, and survival. Moreover, the dynamic balance between levels of the sphingolipids metabolites, ceramide, and SPP, and consequent regulation of opposing signaling pathways, is an important factor that determines whether a cell survives or dies. This ceramide/SPP rheostat is an evolutionarily conserved stress regulatory mechanism influencing growth and survival of yeast. In addition, SPP also has been identified as the ligand for the G-protein-coupled receptors EDG-1, -3, -5, and -6. Binding of SPP to EDG-1 regulates chemotaxis and in vitro angiogenesis of endothelial cells, whereas EDG-5, and possibly EDG-3, are likely the cell surface receptors responsible for cell rounding and neurite retractions induced by SPP. Hence, the studies identify a family of highly specific SPP receptors that are capable of mediating different biological responses. Thus, it is suggested that SPP is a prototype for a novel class of lipid mediators that act both extracellularly as ligands for cell surface receptors and intracellularly as second messengers. Recently, sphingosine kinase was purified to homogeneity and the first mammalian sphingosine kinase, the enzyme responsible for the formation of SPP, was cloned. The studies should provide the necessary tools to develop insight into the biological roles of this important bioactive sphingolipid.

摘要

大量证据表明,1-磷酸鞘氨醇(SPP)可作为细胞内第二信使,调节钙动员、细胞生长和存活。此外,鞘脂代谢产物神经酰胺和SPP水平之间的动态平衡以及由此对相反信号通路的调节,是决定细胞存活或死亡的重要因素。这种神经酰胺/SPP变阻器是一种影响酵母生长和存活的进化保守应激调节机制。此外,SPP还被确定为G蛋白偶联受体EDG-1、-3、-5和-6的配体。SPP与EDG-1的结合调节内皮细胞的趋化性和体外血管生成,而EDG-5以及可能的EDG-3可能是负责SPP诱导的细胞变圆和神经突回缩的细胞表面受体。因此,这些研究确定了一个能够介导不同生物学反应的高度特异性SPP受体家族。因此,有人提出SPP是一类新型脂质介质的原型,它既作为细胞表面受体的配体在细胞外起作用,又作为细胞内第二信使起作用。最近,鞘氨醇激酶被纯化至同质,负责形成SPP的第一种哺乳动物鞘氨醇激酶被克隆。这些研究应提供必要的工具,以深入了解这种重要生物活性鞘脂的生物学作用。

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