Sexton C J, Proby C M, Banks L, Stables J N, Powell K, Navsaria H, Leigh I M
Department of Cell Biology, Wellcome Research Laboratories, Beckenham, U.K.
J Gen Virol. 1993 Apr;74 ( Pt 4):755-61. doi: 10.1099/0022-1317-74-4-755.
We have examined intrinsic and external factors that influence human papillomavirus type 16 (HPV-16)-mediated immortalization of oral keratinocytes. The efficiency with which HPV can immortalize human oral keratinocytes was quantified and a considerable difference in the transfection and immortalization competence of the cells was detected. The ability of HPV-16 to immortalize oral cells appeared to be linked to the age of the culture upon transfection. The addition of dexamethasone to the transfected cultures increased the efficiency of immortalization, possibly indicating a role for a critical level of HPV gene expression in initial outgrowth of immortalized colonies. We also document in detail the changes in the oral keratinocyte induced by HPV-16 immortalization. These include alterations associated with crisis and feeder independence as well as basic changes in keratin expression and differentiation.
我们研究了影响16型人乳头瘤病毒(HPV - 16)介导口腔角质形成细胞永生化的内在和外在因素。对HPV使人类口腔角质形成细胞永生化的效率进行了量化,并检测到细胞在转染和永生化能力方面存在显著差异。HPV - 16使口腔细胞永生化的能力似乎与转染时培养物的年龄有关。向转染后的培养物中添加地塞米松可提高永生化效率,这可能表明HPV基因表达的关键水平在永生化菌落的初始生长中起作用。我们还详细记录了HPV - 16永生化诱导的口腔角质形成细胞的变化。这些变化包括与危机和不依赖饲养层相关的改变,以及角蛋白表达和分化的基本变化。