Uberti J, Lightbody J J, Johnson R M
J Immunol. 1979 Jul;123(1):189-93.
Micromolar deoxyadenosine inhibits leucine uptake during the 1st day of proliferation in mitogen-stimulated lymphocytes if adenosine deaminase is inhibited. This inhibition occurs before DNA synthesis begins, suggesting that deoxyadenosine can affect mitogenesis by mechanisms that do not involve ribonucleotide reductase inhibition. If deoxyadenosine addition to mitogen-stimulated lymphocytes is delayed to the 2nd or 3rd day post-stimulation, inhibition of proliferation is markedly reduced. Although the time dependence of deoxyadenosine toxicity resembles that of adenosine, these compounds appear to inhibit early protein synthesis by different mechanisms: 1) deoxycoformycin markedly potentiates deoxyadenosine but not adenosine; 2) deoxycytidine and thymidine reverse deoxyadenosine toxicity but do not alter adenosine toxicity.
如果腺苷脱氨酶受到抑制,微摩尔浓度的脱氧腺苷会在有丝分裂原刺激的淋巴细胞增殖的第一天抑制亮氨酸摄取。这种抑制在DNA合成开始之前就会发生,这表明脱氧腺苷可以通过不涉及核糖核苷酸还原酶抑制的机制影响有丝分裂。如果在有丝分裂原刺激的淋巴细胞中添加脱氧腺苷的时间推迟到刺激后的第二天或第三天,增殖抑制会明显降低。尽管脱氧腺苷毒性的时间依赖性与腺苷相似,但这些化合物似乎通过不同机制抑制早期蛋白质合成:1)脱氧助间型霉素显著增强脱氧腺苷的作用,但不增强腺苷的作用;2)脱氧胞苷和胸苷可逆转脱氧腺苷的毒性,但不会改变腺苷的毒性。