Sterling J, Stanley M, Gatward G, Minson T
Department of Pathology, University of Cambridge, United Kingdom.
J Virol. 1990 Dec;64(12):6305-7. doi: 10.1128/JVI.64.12.6305-6307.1990.
Human papillomavirus type 16 (HPV-16) is strongly associated with carcinoma of the cervix, but the complete life cycle of the virus cannot be studied because no experimental system is available in which HPV-16 progeny are produced, and there is currently no source of HPV-16 virus particles. Most cell lines that harbor HPV-16 DNA contain the viral genome as integrated or concatenated DNA in which open reading frames are disrupted or deleted, but a human cervical keratinocyte cell line has been described which maintains HPV-16 DNA in monomeric episomal form (M.A. Stanley, H.M. Brown, M.W. Appleby, and A.C. Minson, Int. J. Cancer 43:672-676, 1989). This cell line was induced to form a stratified differentiating epithelium by grafting onto nude mice. Long-term grafts displayed the histological features of a low-grade cervical dysplasia, and terminally differentiated cells contained amplified levels of HPV-16 DNA, virus capsid antigen, and virus particles. This experimental system appears to permit the completion of the HPV-16 life cycle in virus-containing keratinocytes.
16型人乳头瘤病毒(HPV - 16)与宫颈癌密切相关,但由于没有可产生HPV - 16子代病毒的实验系统,且目前没有HPV - 16病毒颗粒来源,因此无法研究该病毒的完整生命周期。大多数含有HPV - 16 DNA的细胞系中,病毒基因组以整合或串联DNA的形式存在,其中开放阅读框被破坏或缺失,但已描述了一种人宫颈角质形成细胞系,其以单体游离型形式维持HPV - 16 DNA(M.A. 斯坦利、H.M. 布朗、M.W. 阿普尔比和A.C. 明森,《国际癌症杂志》43:672 - 676, 1989)。通过移植到裸鼠身上,该细胞系被诱导形成分层分化的上皮组织。长期移植显示出低度宫颈发育异常的组织学特征,终末分化细胞中HPV - 16 DNA、病毒衣壳抗原和病毒颗粒水平升高。该实验系统似乎允许含病毒的角质形成细胞中完成HPV - 16的生命周期。