Tolan D, Conway A M, Steele L, Pyne S, Pyne N J
Department of Physiology and Pharmacology, University of Strathclyde, Glasgow.
Br J Pharmacol. 1996 Sep;119(2):185-6. doi: 10.1111/j.1476-5381.1996.tb15967.x.
We present entirely novel evidence that DL-threo dihydrosphingosine and sphingosine are inhibitors of the extracellular signal-regulated kinase (ERK) signalling cassette in mammalian cells. We show that DL-threo dihydrosphingosine is effective against both growth factor- and G-protein-dependent activation of ERK. We conclude that DL-threo dihydrosphingosine may represent an important pharmacological cell-permeable agent that may be usefully employed to block smooth muscle cell proliferation.
我们提供了全新的证据,表明DL-苏式二氢鞘氨醇和鞘氨醇是哺乳动物细胞中细胞外信号调节激酶(ERK)信号转导盒的抑制剂。我们发现DL-苏式二氢鞘氨醇对生长因子和G蛋白依赖性的ERK激活均有效。我们得出结论,DL-苏式二氢鞘氨醇可能是一种重要的具有细胞通透性的药理试剂,可用于阻止平滑肌细胞增殖。