Furukawa T, Naitoh Y, Kohno H, Tokunaga R, Taketani S
Department of Hygiene, Kansai Medical University, Osaka, Japan.
Life Sci. 1992;50(26):2059-65. doi: 10.1016/0024-3205(92)90572-7.
The effects of the iron-chelator, desferrioxamine, and monoclonal antibodies against transferrin receptors on DNA synthesis and ribonucleotide reductase activity were examined in human leukemia K562 cells. Treatment of the cells with desferrioxamine resulted in decreases of ribonucleotide reductase activity, DNA synthesis, and cell growth. Exposure of the cells to anti-transferrin receptor antibody, 42/6, which blocks iron supplement into cells caused decreases of ribonucleotide reductase activity and DNA synthesis, in a parallel fashion. Decreases of ribonucleotide reductase activity and DNA synthesis by 42/6 were restored by the addition of ferric nitriloacetate. These results indicate that ribonucleotide reductase activity is dependent on the iron-supply and also regulates cell proliferation.
在人白血病K562细胞中检测了铁螯合剂去铁胺和抗转铁蛋白受体单克隆抗体对DNA合成及核糖核苷酸还原酶活性的影响。用去铁胺处理细胞导致核糖核苷酸还原酶活性、DNA合成及细胞生长降低。使细胞暴露于阻断铁进入细胞的抗转铁蛋白受体抗体42/6,会以平行方式导致核糖核苷酸还原酶活性及DNA合成降低。添加次氮基三乙酸铁可恢复42/6所致的核糖核苷酸还原酶活性及DNA合成降低。这些结果表明,核糖核苷酸还原酶活性依赖于铁供应,并且也调节细胞增殖。