Biswal N, Ko U, Akman S, Ross D D, Pollak A, Cimino E
Biochim Biophys Acta. 1983 Aug 2;740(3):271-81. doi: 10.1016/0167-4781(83)90136-7.
To study the nature of virus-cell interaction in persistently infected cells we have examined production of infectious virus, synthesis of viral DNA and DNA polymerase in a human leukemic cell line K562. It was found that only one of three K562 cell lines was permissive for limited growth of HSV-2 and infectious virus was released in a cyclical fashion. Intranuclear inclusions with electron-dense fibrils and particles resembling viral structures were observed in the virus-infected but not control K562 cells. Viral DNA synthesis could not be detected by centrifugation in CsCl density gradients; but was readily identified by Southern blot hydridization of virus-infected intracellular DNA with purified viral DNA. Viral DNa polymerase was synthesized by infected cells during active infectious virus production. In one of the two K562 cell lines that did not produce infectious virus, a few DNA fragments from infected cells were found to hybridize with purified viral DNA. These results suggest that variable lengths of HSV-2 genome can be harbored and propagated by different human leukemic K562 cells.
为了研究持续感染细胞中病毒与细胞相互作用的本质,我们检测了人白血病细胞系K562中传染性病毒的产生、病毒DNA及DNA聚合酶的合成。结果发现,三个K562细胞系中只有一个允许HSV - 2有限生长,且传染性病毒呈周期性释放。在感染病毒的K562细胞中观察到有核内包涵体,其中含有电子致密的纤丝和类似病毒结构的颗粒,而对照K562细胞中未观察到。通过氯化铯密度梯度离心无法检测到病毒DNA的合成;但通过用纯化的病毒DNA对病毒感染的细胞内DNA进行Southern印迹杂交,很容易鉴定出病毒DNA的合成。在有活性的传染性病毒产生过程中,感染细胞合成了病毒DNA聚合酶。在两个不产生传染性病毒的K562细胞系中,有一个细胞系中发现感染细胞的一些DNA片段能与纯化的病毒DNA杂交。这些结果表明,不同的人白血病K562细胞可容纳和传播不同长度的HSV - 2基因组。