Blaho Victoria A, Hla Timothy
Center for Vascular Biology, Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY 10065.
J Lipid Res. 2014 Aug;55(8):1596-608. doi: 10.1194/jlr.R046300. Epub 2014 Jan 23.
Sphingosine 1-phosphate (S1P) is a membrane-derived lysophospholipid that acts primarily as an ex-tracellular signaling molecule. Signals initiated by S1P are transduced by five G protein-coupled receptors, named S1P1-5 Cellular and temporal expression of the S1P receptors (S1PRs) determine their specific roles in various organ systems, but they are particularly critical for regulation of the cardiovascular, immune, and nervous systems, with the most well-known contributions of S1PR signaling being modulation of vascular barrier function, vascular tone, and regulation of lymphocyte trafficking. However, our knowledge of S1PR biology is rapidly increasing as they become attractive therapeutic targets in several diseases, such as chronic inflammatory pathologies, autoimmunity, and cancer. Understanding how the S1PRs regulate interactions between biological systems will allow for greater efficacy in this novel therapeutic strategy as well as characterization of complex physiological networks. Because of the rapidly expanding body of research, this review will focus on the most recent advances in S1PRs.
鞘氨醇-1-磷酸(S1P)是一种源自细胞膜的溶血磷脂,主要作为细胞外信号分子发挥作用。由S1P引发的信号通过五种G蛋白偶联受体进行转导,这些受体被命名为S1P1-5。S1P受体(S1PRs)的细胞和时间表达决定了它们在各种器官系统中的特定作用,但它们对心血管、免疫和神经系统的调节尤为关键,S1PR信号传导最著名的作用是调节血管屏障功能、血管张力以及淋巴细胞运输。然而,随着S1PRs在几种疾病(如慢性炎症性疾病、自身免疫性疾病和癌症)中成为有吸引力的治疗靶点,我们对S1PR生物学的认识正在迅速增加。了解S1PRs如何调节生物系统之间的相互作用,将使这种新型治疗策略具有更高的疗效,并有助于表征复杂的生理网络。由于研究数量迅速增加,本综述将聚焦于S1PRs的最新进展。