Harada S, Koyanagi Y, Nakashima H, Kobayashi N, Yamamoto N
Virology. 1986 Oct 30;154(2):249-58. doi: 10.1016/0042-6822(86)90451-4.
The incubation of Molt-4/HTLV-III cells, human T-lymphotropic virus type III (HTLV-III)/lymphadenopathy-associated virus (LAV)-producer cell line, with more than 0.5 ng/ml of 12-O-tetradecanoylphorbol-13-acetate (TPA) for 2 to 4 days stimulated virus-induced cell killing which resulted in a high production of HTLV-III/LAV. TPA significantly increased the number of plaque-forming viruses released from the cultures as well as viral RNA content. Interestingly, MT-4 cells freshly infected with HTLV-III/LAV treated for 4 days with 0.125 to 2.0 ng/ml of TPA were found to retain the capacity to grow, because TPA inhibited the induction of the virus-specific antigens and cytopathic effects. In contrast to the situation in infected MT-4 cells in liquid cultures, the addition of 0.125 and 0.25 ng/ml of TPA into agarose medium induced large plaques, suggesting that TPA basically enhanced the production of the virus from one infected MT-4 cell. Taken together, the data suggest that TPA enhances the replication of HTLV/III/LAV. These assay systems are shown to be useful for analyzing the induction or suppression of a virus infection by many drugs and other factors in vitro.
将人嗜T淋巴细胞病毒III型(HTLV-III)/淋巴结病相关病毒(LAV)产生细胞系Molt-4/HTLV-III细胞与浓度超过0.5 ng/ml的12-O-十四烷酰佛波醇-13-乙酸酯(TPA)孵育2至4天,可刺激病毒诱导的细胞杀伤,从而导致HTLV-III/LAV的高产量产生。TPA显著增加了从培养物中释放的形成噬斑病毒的数量以及病毒RNA含量。有趣的是,发现用0.125至2.0 ng/ml的TPA处理4天的新鲜感染HTLV-III/LAV的MT-4细胞仍保留生长能力,因为TPA抑制了病毒特异性抗原的诱导和细胞病变效应。与液体培养中感染的MT-4细胞的情况相反,向琼脂糖培养基中添加0.125和0.25 ng/ml的TPA可诱导形成大的噬斑,这表明TPA基本上增强了单个感染的MT-4细胞产生病毒的能力。综上所述,数据表明TPA增强了HTLV/III/LAV的复制。这些检测系统被证明可用于体外分析许多药物和其他因素对病毒感染的诱导或抑制作用。