Suzuki T, He Y, Kashiwagi K, Murakami Y, Hayashi S, Igarashi K
Faculty of Pharmaceutical Sciences, Chiba University, Japan.
Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):8930-4. doi: 10.1073/pnas.91.19.8930.
Exposure of ornithine decarboxylase (ODC; L-ornithine carboxy-lyase, EC 4.1.1.17)-overproducing mouse FM3A cells to micromolar levels of spermine or spermidine caused abnormal accumulation and toxicity of polyamines. This was apparently due to the inefficiency of negative feedback control of polyamine transport by polyamines in ODC-overproducing cells. Since antizyme is the only protein thus far recognized that can interact with ODC, depletion of free antizyme was regarded as the reason for the abnormal accumulation of polyamines. Accordingly, ODC-overproducing cells were transfected with pMAMneoZ1 possessing rat antizyme cDNA under the control of a glucocorticoid-inducible promoter. In the transfected cells, the addition of dexamethasone caused an increase in the amount of antizyme with an apparent molecular mass of 27 kDa, a decrease in the amount of ODC, a decrease in the polyamine transport activity, and the recovery of growth inhibition or cell death. The results indicate that antizyme can regulate not only the amount of ODC but also the activity of polyamine transport.
将过量产生鸟氨酸脱羧酶(ODC;L-鸟氨酸羧基裂解酶,EC 4.1.1.17)的小鼠FM3A细胞暴露于微摩尔水平的精胺或亚精胺会导致多胺异常积累并产生毒性。这显然是由于在过量产生ODC的细胞中,多胺对多胺转运的负反馈控制效率低下所致。由于抗酶是迄今为止唯一被认为能与ODC相互作用的蛋白质,游离抗酶的消耗被视为多胺异常积累的原因。因此,用在糖皮质激素诱导型启动子控制下携带大鼠抗酶cDNA的pMAMneoZ1转染过量产生ODC的细胞。在转染细胞中,添加地塞米松会导致表观分子量为27 kDa的抗酶量增加、ODC量减少、多胺转运活性降低以及生长抑制或细胞死亡的恢复。结果表明,抗酶不仅可以调节ODC的量,还可以调节多胺转运的活性。