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人乳头瘤病毒16型E5蛋白可抑制人角质形成细胞筏培养物中肿瘤坏死因子相关凋亡诱导配体(TRAIL)和Fas配体(FasL)介导的细胞凋亡。

The HPV-16 E5 protein inhibits TRAIL- and FasL-mediated apoptosis in human keratinocyte raft cultures.

作者信息

Kabsch Kirsten, Mossadegh Nina, Kohl Annette, Komposch Gerda, Schenkel Johannes, Alonso Angel, Tomakidi Pascal

机构信息

German Cancer Research Center, University of Heidelberg, Heidelberg, Germany.

出版信息

Intervirology. 2004;47(1):48-56. doi: 10.1159/000076642.

Abstract

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.

摘要

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。

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