Marcellus R C, Lavoie J N, Boivin D, Shore G C, Ketner G, Branton P E
Departments of Biochemistry, McGill University, Montréal, Québec, Canada H3G 1Y6.
J Virol. 1998 Sep;72(9):7144-53. doi: 10.1128/JVI.72.9.7144-7153.1998.
Previous studies by our group showed that infection of human and rodent cells by human adenovirus type 5 (Ad5) results in the induction of p53-independent apoptosis and cell death that are dependent upon transactivation of early region 4 (E4). To identify which E4 products are involved, studies were conducted with p53-deficient human SAOS-2 cells infected with various Ad5 E4 mutants. An E4orf6-deficient mutant was defective in cell killing, whereas another that expressed only E4orf6 and E4orf4 killed like wild-type virus, suggesting that E4orf6 may be responsible for cytotoxicity; however, a mutant expressing only E4orf4 induced high levels of cell death, indicating that this E4 product may also be able to induce cytotoxicity. To define the E4 cell death-inducing functions more precisely, cDNAs encoding individual E4 products were introduced into cells by DNA transfection in the absence of other Ad5 proteins. In cotransfections with a cDNA encoding firefly luciferase, enzymatic activity was high in all cases except with E4orf4, where luciferase levels were less than 20% of those in controls. In addition, drug selection of several cell types following transfection with retroviral vector DNA encoding individual E4 products as well as puromycin resistance yielded a large number of cell colonies except when E4orf4 was expressed. These data demonstrated that E4orf4 is the only E4 product capable of independent cell killing. Cell death induced by E4orf4 was due to apoptosis, as evidenced by 4',6-diamidino-2-phenylindole (DAPI) staining of cell nuclei in E4orf4-expressing cells. Thus, although E4orf6 may play some role, these results suggested that E4orf4 may be the major E4 product responsible for induction of p53-independent apoptosis.
我们小组之前的研究表明,人5型腺病毒(Ad5)感染人和啮齿动物细胞会导致p53非依赖性凋亡和细胞死亡,这依赖于早期区域4(E4)的反式激活。为了确定哪些E4产物参与其中,我们用感染了各种Ad5 E4突变体的p53缺陷型人SAOS-2细胞进行了研究。一种E4orf6缺陷型突变体在细胞杀伤方面存在缺陷,而另一种仅表达E4orf6和E4orf4的突变体的杀伤作用与野生型病毒相似,这表明E4orf6可能是细胞毒性的原因;然而,一种仅表达E4orf4的突变体诱导了高水平的细胞死亡,表明这种E4产物也可能能够诱导细胞毒性。为了更精确地定义E4诱导细胞死亡的功能,在没有其他Ad5蛋白的情况下,通过DNA转染将编码单个E4产物的cDNA导入细胞。在与编码萤火虫荧光素酶的cDNA共转染时,除了E4orf4的情况外,所有情况下酶活性都很高,在E4orf4的情况下,荧光素酶水平不到对照的20%。此外,用编码单个E4产物的逆转录病毒载体DNA转染几种细胞类型并进行药物筛选以及嘌呤霉素抗性筛选,除了表达E4orf4的情况外,产生了大量细胞集落。这些数据表明,E4orf4是唯一能够独立导致细胞死亡的E4产物。E4orf4诱导的细胞死亡是由于凋亡,这通过对表达E4orf4的细胞进行细胞核的4',6-二脒基-2-苯基吲哚(DAPI)染色得到证明。因此,尽管E4orf6可能起一些作用,但这些结果表明E4orf4可能是负责诱导p53非依赖性凋亡的主要E4产物。