Suk W A, Long C W
J Gen Virol. 1981 Jan;52(Pt 1):189-94. doi: 10.1099/0022-1317-52-1-189.
Enhancement of endogenous xenotropic virus expression has been found upon treatment with tetrapeptides of a high-passage clone of Balb/c (K-Balb) mouse cells transformed with Kirsten sarcoma virus. Tuftsin (Thr-Lys-Pro-Arg) and kentsin (Thr-Pro-Arg-Lys) increased the expression of virus that was infectious for rat, but not mouse, cells in a concentration-dependent fashion. The enhancement of virus expression by the tetrapeptides was proportional to the spontaneous release of virus. The infectivity of the enhanced virus was neutralized by goat anti-RLV gp70 serum. Actinomycin D inhibited the induction of virus, suggesting that enhanced expression required de novo RNA synthesis. The effects observed using K-Balb cells offer an opportunity to study the many biological effects of these peptides in a fibroblast culture system.
在用 Kirsten 肉瘤病毒转化的 Balb/c(K-Balb)小鼠细胞的高传代克隆的四肽处理后,已发现内源性嗜异性病毒表达增强。促吞噬素(苏氨酸-赖氨酸-脯氨酸-精氨酸)和肯辛(苏氨酸-脯氨酸-精氨酸-赖氨酸)以浓度依赖的方式增加了对大鼠而非小鼠细胞具有感染性的病毒的表达。四肽对病毒表达的增强与病毒的自发释放成正比。增强病毒的感染性被山羊抗 RLV gp70 血清中和。放线菌素 D 抑制病毒的诱导,表明增强的表达需要从头合成 RNA。使用 K-Balb 细胞观察到的这些效应为在成纤维细胞培养系统中研究这些肽的多种生物学效应提供了机会。