Kyo S, Klumpp D J, Inoue M, Kanaya T, Laimins L A
Department of Obstetrics and Gynecology, School of Medicine, Kanazawa University, Ishikawa, Japan.
J Gen Virol. 1997 Feb;78 ( Pt 2):401-11. doi: 10.1099/0022-1317-78-2-401.
E6 and E7 oncoproteins of human papillomavirus (HPV) play significant roles in the pathogenesis of cervical cancer. However, the pattern of E6/E7 expression during the productive virus life cycle in differentiating epithelia of the uterine cervix remains unclear. In addition, little is known about the cellular factors regulating E6/E7 expression in differentiating epithelia. In the present study, using transient expression assays and DNA binding assays, we demonstrated that E6/E7 transcription is critically regulated by the cellular factor AP1, a Jun/Fos heterodimer complex. Immunohistochemical analyses of various uterine cervical lesions showed AP1 expression in lower cell layers of normal cervix and low-grade cervical intraepithelial neoplasia (CIN), while it was detected throughout all layers in high-grade CIN and invasive cancer. In situ RNA-RNA hybridization analyses of organotypic raft culture specimens of an HPV-31-containing cell line revealed that E6/E7 transcripts were expressed in most cell layers, with reduced expression in differentiated cells. This pattern of HPV expression correlated with the pattern of AP1 expression detected by immunohistochemical analyses. These findings suggest that E6/E7 expression in differentiating epithelia is dependent on AP1, which appears to be associated with proliferative activity of the cells. Since E6/E7 expression induces cell proliferation, co-expression of AP1 and E6/E7 in undifferentiated cell layers might create a positive regulatory loop, probably contributing to maintenance of initial HPV infection and subsequent activation in basal and suprabasal cell layers.
人乳头瘤病毒(HPV)的E6和E7癌蛋白在宫颈癌的发病机制中发挥着重要作用。然而,在子宫颈分化上皮细胞的病毒生产性生命周期中,E6/E7的表达模式仍不清楚。此外,关于调节分化上皮细胞中E6/E7表达的细胞因子也知之甚少。在本研究中,我们通过瞬时表达分析和DNA结合分析证明,E6/E7转录受细胞因子AP1(一种Jun/Fos异二聚体复合物)的严格调控。对各种子宫颈病变的免疫组织化学分析显示,AP1在正常子宫颈和低级别子宫颈上皮内瘤变(CIN)的较低细胞层中表达,而在高级别CIN和浸润性癌的所有细胞层中均有检测到。对含HPV-31细胞系的器官型筏培养标本进行原位RNA-RNA杂交分析发现,E6/E7转录本在大多数细胞层中表达,在分化细胞中表达减少。这种HPV表达模式与免疫组织化学分析检测到的AP1表达模式相关。这些发现表明,分化上皮细胞中的E6/E7表达依赖于AP1,而AP1似乎与细胞的增殖活性有关。由于E6/E7表达诱导细胞增殖,未分化细胞层中AP1和E6/E7的共表达可能会形成一个正调控环,这可能有助于维持最初的HPV感染以及随后在基底细胞层和基底上层细胞层中的激活。