Schmidt A, Crisp B, Krause D, Silverman R H, Herberman R B, Ortaldo J R
Nat Immun Cell Growth Regul. 1987;6(1):19-27.
Pretreatment of human large granular lymphocytes (LGL) or unseparated peripheral blood mononuclear cells with interferon (IFN) resulted in a significant augmentation of natural killer (NK) activity. This increase was paralleled by an increase in the 2'-5'A synthetase activity. In order to investigate the possibility that IFN might be inducing augmentation of NK cells via the 2'-5'A pathway, we tested the effects of nonphosphorylated core material [(A2'p)2A] and of the triphosphorylated form of the 2'-5'A [ppp(A2'p)2A]. The core material had no detectable effect on NK activity. In contrast, when experiments were performed with the triphosphorylated form of 2'-5'A, NK activity was stimulated. In order to achieve activation, permeabilization of LGL with calcium chloride was necessary and, under these conditions, a dose-dependent augmentation of NK activity was seen. However, the calcium treatment had considerable toxic effects on basal levels of NK activity. Collectively, these results suggest that IFN may be inducing augmentation of NK activity via the 2'-5'A pathway. Further studies will be necessary to determine the effects of IFN and/or 2'-5'A on subsequent activation steps in the process leading to cytotoxicity by NK cells.
用干扰素(IFN)对人大颗粒淋巴细胞(LGL)或未分离的外周血单个核细胞进行预处理,可显著增强自然杀伤(NK)活性。这种增加与2'-5'A合成酶活性的增加平行。为了研究IFN可能通过2'-5'A途径诱导NK细胞增强的可能性,我们测试了非磷酸化核心物质[(A2'p)2A]和2'-5'A的三磷酸化形式[ppp(A2'p)2A]的作用。核心物质对NK活性没有可检测到的影响。相反,当用2'-5'A的三磷酸化形式进行实验时,NK活性受到刺激。为了实现激活,用氯化钙使LGL通透化是必要的,在这些条件下,可观察到NK活性呈剂量依赖性增强。然而,钙处理对NK活性的基础水平有相当大的毒性作用。总体而言,这些结果表明IFN可能通过2'-5'A途径诱导NK活性增强。需要进一步研究以确定IFN和/或2'-5'A对NK细胞导致细胞毒性过程中后续激活步骤的影响。