牛乳头瘤病毒感染病变原代培养物作为研究代谢失调的模型

R. C. Stocco
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引用次数: 6

摘要

牛乳头状瘤病毒(BPV)是牛乳头状瘤病的病原,这种疾病的特征是存在多个乳头状瘤,可以退化或进展为恶性肿瘤。由于与人乳头瘤病毒(HPV)的病理相似,BPV被认为是研究乳头瘤病毒相关致癌过程的原型。虽然很明显BPV和HPV都可以与宿主染色质相互作用,但由于对乳头瘤病毒感染病变的原代培养物很少关注,这些病毒与细胞代谢的相互作用仍未得到充分研究。因此,本研究分析了皮肤乳头状瘤、纤维乳头状瘤和食管癌(EC)来源细胞的能量代谢,包括线粒体膜电位(ΔΨm)和活性氧(ROS)作为模型来评估细胞代谢。将这些细胞培养至第六代,利用BPV-1、2和4的特异性引物进行BPV DNA序列的PCR鉴定。PCR结果显示,在所分析的6个传代中至少存在并维持一种BPV型。无BPV DNA序列的正常皮肤细胞作为对照。能量代谢结果显示纤维乳头瘤细胞和EC细胞中ΔΨm的缺失,表明代谢开关与有氧糖酵解的激活相兼容。皮肤乳头瘤和正常皮肤细胞维持ΔΨm。矛盾的是,皮肤乳头瘤和纤维乳头瘤表现出高水平的ROS产生,而EC细胞降低了ROS水平,加强了糖酵解代谢的激活。我们的研究结果表明,代谢开关是由BPV E6癌蛋白介导的,因为在正常细胞中添加这种癌蛋白会促进氧化应激。氧化应激能够激活乳头状瘤和纤维乳头状瘤细胞中的STAT3核因子,促进代谢失调。这些数据表明,原代培养是研究BPV与细胞代谢相互作用的有效模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Cultures Derived From Bovine Papillomavirus-Infected Lesions As Model To Study Metabolic Deregulation
Bovine papillomavirus (BPV) is the etiological agent of bovine papillomatosis, disease characterized by the presence of multiple papillomas that can regress or to progress to malignances. Due to the pathological similarities with the human papillomavirus (HPV), BPV is considered a prototype to study the papillomavirus-associated oncogenic process. Although it is clear that both BPV and HPV can interact with host chromatin, the interaction of these viruses with cell metabolism remains understudied due to the little attention given to primary cultures derived from papillomavirus-infected lesions. Thus, this study analyzed the energy metabolism, including the mitochondrial membrane potential (ΔΨm) and Reactive Oxygen Species (ROS) of cells derived from cutaneous papilloma, fibropapilloma and Esophageal Carcinoma (EC) as model to evaluate the cell metabolism. These cells were cultivated until sixth passage and subjected to BPV DNA sequences identification by PCR using specific primers to BPV-1, 2 and 4. PCR results showed the presence and maintenance of at least one BPV type along the six passages analyzed. Cells derived from normal skin, without BPV DNA sequences were used as control. Results of energy metabolism showed the loss of ΔΨm in fibropapilloma and EC cells, suggesting a metabolic switch compatible to the activation of aerobic glycolysis. Cutaneous papilloma and normal skin cells showed the maintenance of ΔΨm. Paradoxically, cutaneous papilloma and fibropapilloma presented high levels of ROS production, while the EC cells reduced the ROS levels, reinforcing the activation of glycolytic metabolism. Our results suggest that the metabolic switch is mediated by BPV E6 oncoprotein, since the addition of this oncoprotein in normal cells promoted the oxidative stress. The oxidative stress showed able to activate the STAT3 nuclear factor in papilloma and fibropapilloma cells, contributing to metabolic deregulation. These data suggest that primary cultures are useful model to study the interaction between BPV and cell metabolism.
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