Hudson J B, Bedell M A, McCance D J, Laiminis L A
Howard Hughes Medical Institute, Chicago, Illinois.
J Virol. 1990 Feb;64(2):519-26. doi: 10.1128/JVI.64.2.519-526.1990.
The E6-E7 region of human papillomavirus types 16 and 18 is selectively retained and expressed in cervical carcinoma cells. In cultured human keratinocytes, expression of the E6 and E7 open reading frames of human papillomavirus type 18, under the control of its homologous promoter, resulted in high-frequency immortalization. Furthermore, by using a system that allows for stratification of keratinocytes in vitro (raft system), we observed that the morphological differentiation of these E6-E7 immortalized cells was altered such that parabasal cells extended throughout most of the epithelium, with abnormal nuclei present in the upper regions. Examination of E6-E7-expressing cell lines in the raft system at a later passage revealed that complete loss of morphological differentiation had occurred. E7 alone was a much less effective immortalizing agent than E6 and E7 together and acted only minimally to alter morphological differentiation in vitro. No such activities were found for E6 alone. High-frequency transformation of human epithelial cells thus appears to require expression of both E6 and E7 gene products.
人乳头瘤病毒16型和18型的E6 - E7区域在宫颈癌细胞中被选择性保留并表达。在培养的人角质形成细胞中,人乳头瘤病毒18型的E6和E7开放阅读框在其同源启动子的控制下表达,导致高频永生化。此外,通过使用一种允许在体外对角质形成细胞进行分层的系统(筏系统),我们观察到这些E6 - E7永生化细胞的形态分化发生了改变,使得基底旁细胞延伸至大部分上皮组织,在上层区域存在异常细胞核。在筏系统中对后期传代的表达E6 - E7的细胞系进行检查发现,形态分化已完全丧失。单独的E7作为永生化剂的效果远不如E6和E7共同作用,并且在体外对形态分化的改变作用极小。单独的E6未发现此类活性。因此,人上皮细胞的高频转化似乎需要E6和E7基因产物的共同表达。