Kabsch Kirsten, Mossadegh Nina, Kohl Annette, Komposch Gerda, Schenkel Johannes, Alonso Angel, Tomakidi Pascal
German Cancer Research Center, University of Heidelberg, Heidelberg, Germany.
Intervirology. 2004;47(1):48-56. doi: 10.1159/000076642.
By using raft cultures of the polyclonal HaCaT cell lines stably transfected either with E5 (HaCaT/E5) or the empty vector (HaCaT/pMSG) as reference, we investigated the effect of the human papillomavirus type 16 (HPV-16) E5 protein on apoptosis. In comparison to conventional monolayer cultures this model system allows analysis of apoptosis under more tissue-like conditions by mimicking the stratified organization of a normal surface epithelium. Apoptosis was triggered either by FasL or TRAIL. Execution of the death program was checked at early and late stages by monitoring procaspase-3 cleavage and DNA fragmentation, respectively. Rafts of E5-expressing keratinocytes were completely protected from apoptosis and showed a background of apoptotic cells as low as the untreated cultures. In contrast, the HaCaT/pMSG cultures revealed a dramatic increase in apoptotic cells upon ligand treatment throughout the epithelial compartment. We conclude that the presence of the HPV-16 E5 protein in our tissue-like model prevents FasL- or TRAIL-mediated apoptosis.
通过使用稳定转染E5(HaCaT/E5)或空载体(HaCaT/pMSG)的多克隆HaCaT细胞系的筏式培养物作为对照,我们研究了人乳头瘤病毒16型(HPV-16)E5蛋白对细胞凋亡的影响。与传统的单层培养相比,该模型系统通过模拟正常表面上皮的分层组织,能够在更接近组织的条件下分析细胞凋亡。细胞凋亡由FasL或TRAIL触发。分别通过监测procaspase-3裂解和DNA片段化,在早期和晚期检查死亡程序的执行情况。表达E5的角质形成细胞筏完全免受细胞凋亡影响,并且显示出与未处理培养物一样低的凋亡细胞背景。相反,HaCaT/pMSG培养物在配体处理后,整个上皮区室的凋亡细胞显著增加。我们得出结论,在我们的组织样模型中,HPV-16 E5蛋白的存在可防止FasL或TRAIL介导的细胞凋亡。