Bardell D, Metcalf T G
Infect Immun. 1974 Jul;10(1):83-7. doi: 10.1128/iai.10.1.83-87.1974.
Beta-glucuronidase activity was investigated during a 48-h period in which virus replication and changes in cell morphology occurred. Infection of an established line of chimpanzee liver cells with either nononcogenic adenovirus 5 or highly oncogenic adenovirus 12 under one-step growth conditions produced differing patterns of enzyme activity. There was an increase in total activity and also enhanced leakage of beta-glucuronidase from cells infected with adenovirus 12. In contrast, the enzymatic pattern of cells infected with adenovirus 5 was similar to that of uninfected cells. Hydrocortisone prevented the abnormal release of beta-glucuronidase from adenovirus 12-infected cells. The compound had no effect on total enzyme activity or on virus replication and the development of cytopathology.
在48小时内对β-葡萄糖醛酸酶活性进行了研究,在此期间发生了病毒复制和细胞形态变化。在一步生长条件下,用非致癌性腺病毒5或高致癌性腺病毒12感染已建立的黑猩猩肝细胞系,产生了不同的酶活性模式。感染腺病毒12的细胞中,β-葡萄糖醛酸酶的总活性增加,且从细胞中泄漏的情况也增强。相比之下,感染腺病毒5的细胞的酶模式与未感染细胞相似。氢化可的松可防止腺病毒12感染细胞中β-葡萄糖醛酸酶的异常释放。该化合物对总酶活性、病毒复制及细胞病理学发展均无影响。