Fresa K L, Karjalainen H E, Tevethia S S
J Immunol. 1987 Feb 15;138(4):1215-20.
The susceptibility of mouse cells expressing full-length or truncated transforming protein (T antigen) of simian virus 40 (SV40) to lysis by murine natural killer (NK) cells was assessed. For these studies, C57BL/6 mouse embryo fibroblasts (B6/MEF) were transformed by transfection with SV40 DNA encoding the entire T antigen. The transformed cell lines were tested for susceptibility to lysis by nonimmune CBA splenocytes as a source of NK cells and to lysis by C57BL/6, SV40-specific cytolytic T cells (CTL). It was found that 13 of 15 clonally derived, SV40-transformed H-2b cell lines were susceptible to lysis by NK cells. However, there was some variation in their susceptibility to lysis by NK cells. There was no correlation between susceptibility to lysis by SV40-specific CTL and to lysis by NK cells. Cells transfected with a plasmid which encodes only the N-terminal half of the SV40 T antigen were consistently less susceptible to lysis by NK cells, suggesting that expression of only the N-terminus of the T antigen was insufficient for optimal susceptibility to lysis by NK cells. Primary mouse embryo fibroblasts transformed by human adenovirus type 5 E1 region DNA were also found to be susceptible to NK cell-mediated lysis. Lysis of SV40-transformed cells by nonimmune CBA splenocytes was mediated by NK cells because: lysis was augmented when the effector cells were treated with interferon before assay; and lysis was abrogated when the effector cells were obtained from mice that had been depleted of NK activity by treatment with antiserum against the asialo GM1 surface marker. These results indicate that primary mouse cells which are transformed by SV40 and which express the native T antigen are susceptible to lysis by mouse NK cells. Conversely, cells transformed by a plasmid encoding only the N-terminal half of the T antigen express reduced susceptibility to lysis by NK cells.
评估了表达猿猴病毒40(SV40)全长或截短转化蛋白(T抗原)的小鼠细胞被小鼠自然杀伤(NK)细胞裂解的敏感性。对于这些研究,用编码完整T抗原的SV40 DNA转染C57BL/6小鼠胚胎成纤维细胞(B6/MEF)进行转化。测试转化细胞系对作为NK细胞来源的非免疫CBA脾细胞裂解的敏感性以及对C57BL/6、SV40特异性细胞毒性T细胞(CTL)裂解的敏感性。发现15个克隆衍生的SV40转化的H-2b细胞系中有13个对NK细胞裂解敏感。然而,它们对NK细胞裂解的敏感性存在一些差异。对SV40特异性CTL裂解的敏感性与对NK细胞裂解的敏感性之间没有相关性。用仅编码SV40 T抗原N端一半的质粒转染的细胞对NK细胞裂解的敏感性始终较低,这表明仅T抗原N端的表达不足以使细胞对NK细胞裂解具有最佳敏感性。还发现,用人腺病毒5型E1区DNA转化的原代小鼠胚胎成纤维细胞也对NK细胞介导的裂解敏感。非免疫CBA脾细胞对SV40转化细胞的裂解由NK细胞介导,原因如下:在检测前用干扰素处理效应细胞时裂解增强;当效应细胞取自用抗唾液酸GM1表面标志物抗血清处理而耗尽NK活性的小鼠时,裂解被消除。这些结果表明,被SV40转化并表达天然T抗原的原代小鼠细胞对小鼠NK细胞裂解敏感。相反,用仅编码T抗原N端一半的质粒转化的细胞对NK细胞裂解的敏感性降低。