Weber J M, Stewart R B
J Gen Virol. 1975 Sep;28(3):363-72. doi: 10.1099/0022-1317-28-3-363.
Treatment of L cells with 3 to 10 mM 3':5'-cyclic adenosine monophosphate (cAMP) in the presence of interferon was found to potentiate the development of antiviral activity. The dose response of interferon activity at various time periods in the presence and absence of cAMP indicated that potentiation of interferon activity by cAMP occurred at an early stage in the development of antiviral activity. Among the analogues of cAMP tested for interferon-potentiating activity, only the acylated derivatives were found to be active. Combined L-epinephrine and theophylline treatment of cells elevated cellular cAMP levels and also potentiated interferon-mediated antiviral activity. Interferon was also found to elevate cAMP levels in L cells. This activity was limited to biologically active interferon and antagonized the depression of cAMP associated with vesicular stomatitis virus (VSV) infection of L cells. These observations suggest that some aspects of interferon's biological activity is associated with an alteration in cellular levels of cAMP.
发现在存在干扰素的情况下,用3至10 mM的3':5'-环磷酸腺苷(cAMP)处理L细胞可增强抗病毒活性的发展。在有和没有cAMP的情况下,不同时间段干扰素活性的剂量反应表明,cAMP对干扰素活性的增强作用发生在抗病毒活性发展的早期阶段。在测试的cAMP类似物中,只有酰化衍生物具有干扰素增强活性。联合使用L-肾上腺素和茶碱处理细胞可提高细胞内cAMP水平,也可增强干扰素介导的抗病毒活性。还发现干扰素可提高L细胞中的cAMP水平。这种活性仅限于具有生物活性的干扰素,并可拮抗与L细胞感染水疱性口炎病毒(VSV)相关的cAMP降低。这些观察结果表明,干扰素生物活性的某些方面与细胞内cAMP水平的改变有关。