Molecular Cancer Research Centre (MKFZ), Charité University Medical School (CVK), Berlin, Germany.
Arch Immunol Ther Exp (Warsz). 2012 Feb;60(1):3-12. doi: 10.1007/s00005-011-0159-5. Epub 2011 Dec 8.
It is well established that the lysophospholipid and signalling molecule sphingosine 1-phosphate (S1P) has many important functions in immune surveillance. S1P is produced from sphingosine by two distinct sphingosine kinases, SphK1 and SphK2, and acts as an intracellular messenger and as an extracellular ligand of five G protein-coupled cell surface receptors designated S1P(1)-S1P(5). S1P not only regulates peripheral lymphocyte circulation, but also influences their differentiation, activation, infiltration, and local positioning. The therapeutic value of modulating S1P metabolism and S1P receptor function is currently tested in clinical trials and holds great promise for treatment of different autoimmune diseases. Despite its obvious contribution to immune regulation, the analysis of S1P is still challenging. A major obstacle is the difficulty to analyze S1P locally in tissues and within cells due to its high metabolic turnover and the limited resolution of current analytical techniques like liquid chromatography and mass spectrometry. This review focuses on recent advancements to our understanding how different sources of S1P contribute to immune function, and how changes in production, secretion, and degradation of S1P can influence immune responses.
众所周知,溶血磷脂和信号分子 1-磷酸鞘氨醇(S1P)在免疫监视中具有许多重要功能。S1P 由鞘氨醇通过两种不同的鞘氨醇激酶(SphK1 和 SphK2)产生,作为细胞内信使和五个 G 蛋白偶联细胞表面受体(命名为 S1P(1)-S1P(5))的细胞外配体。S1P 不仅调节外周淋巴细胞循环,还影响其分化、激活、浸润和局部定位。调节 S1P 代谢和 S1P 受体功能的治疗价值目前正在临床试验中进行测试,为治疗不同的自身免疫性疾病带来了巨大的希望。尽管 S1P 对免疫调节有明显的贡献,但对 S1P 的分析仍然具有挑战性。一个主要障碍是由于其高代谢周转率和当前分析技术(如液相色谱和质谱)的分辨率有限,难以在组织和细胞内分析 S1P。本综述重点介绍了我们对 S1P 的不同来源如何有助于免疫功能的理解的最新进展,以及 S1P 的产生、分泌和降解的变化如何影响免疫反应。