Zhang H, Desai N N, Olivera A, Seki T, Brooker G, Spiegel S
Department of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, DC 20007.
J Cell Biol. 1991 Jul;114(1):155-67. doi: 10.1083/jcb.114.1.155.
Sphingosine, a metabolite of membrane sphingolipids, regulates proliferation of quiescent Swiss 3T3 fibroblasts (Zhang, H., N. E. Buckley, K. Gibson. and S. Spiegel. 1990. J. Biol. Chem. 265:76-81). The present study provides new insights into the formation and function of a unique phospholipid, a metabolite of sphingosine, which was unequivocally identified as sphingosine-1-phosphate. The rapid increase in 32P-labeled sphingosine-1-phosphate levels induced by sphingosine was concentration dependent and correlated with its effect on DNA synthesis. Similar to the mitogenic effects of sphingosine, low concentrations of sphingosine-1-phosphate stimulated DNA synthesis and induced pronounced morphological alterations. Both sphingosine and sphingosine-1-phosphate stimulated DNA synthesis in cells made protein kinase C deficient by prolonged treatment with phorbol ester and sphingosine still elicited similar increases in sphingosine-1-phosphate levels in these cells. Although both sphingosine and sphingosine-1-phosphate acted synergistically with a wide variety of growth factors, there was no additive or synergistic effect in response to a combination of sphingosine and sphingosine-1-phosphate. Using a digital imaging system for measurement of calcium changes, we observed that both sphingosine and sphingosine-1-phosphate are potent calcium-mobilizing agonists in viable 3T3 fibroblasts. The rapid rise in cytosolic free calcium was independent of the presence of calcium in the external medium, indicating that the response is due to the mobilization of calcium from internal store. Our results suggest that sphingosine-1-phosphate may be a component of the intracellular second messenger system that is involved in calcium release and the regulation of cell growth induced by sphingosine.
鞘氨醇是膜鞘脂的一种代谢产物,可调节静止的瑞士3T3成纤维细胞的增殖(Zhang, H., N. E. Buckley, K. Gibson.和S. Spiegel. 1990.《生物化学杂志》265:76 - 81)。本研究为一种独特的磷脂(鞘氨醇的一种代谢产物)的形成和功能提供了新的见解,该磷脂被明确鉴定为鞘氨醇-1-磷酸。鞘氨醇诱导的32P标记的鞘氨醇-1-磷酸水平的快速升高呈浓度依赖性,且与其对DNA合成的影响相关。与鞘氨醇的促有丝分裂作用相似,低浓度的鞘氨醇-1-磷酸刺激DNA合成并引起明显的形态改变。鞘氨醇和鞘氨醇-1-磷酸均可刺激经佛波酯长期处理而使蛋白激酶C缺乏的细胞中的DNA合成,并且鞘氨醇仍能使这些细胞中的鞘氨醇-1-磷酸水平出现类似的升高。尽管鞘氨醇和鞘氨醇-1-磷酸均与多种生长因子协同作用,但对于鞘氨醇和鞘氨醇-1-磷酸的组合并无相加或协同效应。使用数字成像系统测量钙变化,我们观察到鞘氨醇和鞘氨醇-1-磷酸在存活的3T3成纤维细胞中均是有效的钙动员激动剂。胞质游离钙的快速升高与细胞外培养基中钙的存在无关,表明该反应是由于从内部储存库中动员钙所致。我们的结果表明,鞘氨醇-1-磷酸可能是细胞内第二信使系统的一个组成部分,参与钙释放以及鞘氨醇诱导的细胞生长调节。