Ng Mei Li, Wadham Carol, Sukocheva Olga A
Centenary Institute of Cancer Medicine and Cell Biology, Sydney, NSW 2050, Australia.
Children's Cancer Institute Australia, Lowy Cancer Research Centre, University of New South Wales, Randwick, NSW 2031, Australia.
Int J Mol Med. 2017 Feb;39(2):243-252. doi: 10.3892/ijmm.2017.2855. Epub 2017 Jan 11.
Sphingosine kinase (SphK) is an important signalling enzyme that catalyses the phosphorylation of sphingosine (Sph) to form sphingosine‑1‑phosphate (S1P). The multifunctional lipid, S1P binds to a family of five G protein-coupled receptors (GPCRs). As an intracellular second messenger, S1P activates key signalling cascades responsible for the maintenance of sphingolipid metabolism, and has been implicated in the progression of cancer, and the development of other inflammatory and metabolic diseases. SphK and S1P are critical molecules involved in the regulation of various cellular metabolic processes, such as cell proliferation, survival, apoptosis, adhesion and migration. There is strong evidence supporting the critical roles of SphK and S1P in the progression of diabetes mellitus, including insulin sensitivity and insulin secretion, pancreatic β‑cell apoptosis, and the development of diabetic inflammatory state. In this review, we summarise the current state of knowledge for SphK/S1P signalling effects, associated with the development of insulin resistance, pancreatic β‑cell death and the vascular complications of diabetes mellitus.
鞘氨醇激酶(SphK)是一种重要的信号酶,可催化鞘氨醇(Sph)磷酸化形成1-磷酸鞘氨醇(S1P)。多功能脂质S1P可与一类由五个成员组成的G蛋白偶联受体(GPCR)相结合。作为一种细胞内第二信使,S1P可激活负责维持鞘脂代谢的关键信号级联反应,并与癌症进展以及其他炎症和代谢性疾病的发展有关。SphK和S1P是参与调节各种细胞代谢过程的关键分子,如细胞增殖、存活、凋亡、黏附和迁移。有强有力的证据支持SphK和S1P在糖尿病进展中发挥的关键作用,包括胰岛素敏感性和胰岛素分泌、胰腺β细胞凋亡以及糖尿病炎症状态的发展。在本综述中,我们总结了与胰岛素抵抗、胰腺β细胞死亡和糖尿病血管并发症发展相关的SphK/S1P信号传导效应的当前知识状态。