Department of Anatomy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Int J Cancer. 2010 Oct 1;127(7):1570-83. doi: 10.1002/ijc.25173.
Epstein-Barr virus (EBV) infection has been postulated to be an early event involved in the pathogenesis of nasopharyngeal carcinomas (NPC). The lack of representative premalignant nasopharyngeal epithelial cell system for EBV infection has hampered research investigation into the regulation and involvement of EBV infection in NPC pathogenesis. We have compared the efficiency of EBV infection in nasopharyngeal epithelial cells with different biological properties including immortalized, primary and cancerous nasopharyngeal epithelial cells. EBV infection could be achieved in all the nasopharyngeal epithelial cells examined with variable infection rate. TGF-beta effectively enhanced EBV infection into nasopharyngeal epithelial cells both in the immortalized and primary nasopharyngeal epithelial cells. Stable infection of EBV was achieved in a telomerase-immortalized nasopharyngeal epithelial cell line, NP460hTert. The expression pattern of EBV-encoded genes and biological properties of this EBV infected cell line on long-term propagation were monitored. The EBV-infected nasopharyngeal epithelial cells acquired anchorage-independent growth and exhibited invasive growth properties on prolonged propagation. A distinguished feature of this EBV-infected nasopharyngeal epithelial cell model was its enhanced ability to survive under growth factor and nutrient starvation. This was evidenced by the suppressed activation of apoptotic markers and sustained activation of pAkt of EBV-infected cells compared to control cells under nutrient starvation. Examination of cytokine profiles of EBV-infected NP460hTert cells to nutrient and growth factor deprivation revealed upregulation of expression of MCP-1 and GRO-alpha. The establishment of a stable EBV infection model of premalignant nasopharyngeal epithelial cells will facilitate research investigation into the pathogenic role of EBV in NPC development.
EBV 感染被认为是参与鼻咽癌(NPC)发病机制的早期事件。缺乏代表性的鼻咽癌前上皮细胞系统进行 EBV 感染研究,阻碍了 EBV 感染在 NPC 发病机制中的调控和参与研究。我们比较了不同生物学特性的鼻咽上皮细胞中 EBV 感染的效率,包括永生化、原代和癌细胞鼻咽上皮细胞。所有被检测的鼻咽上皮细胞都可以实现 EBV 感染,感染率不同。TGF-β能有效地增强永生化和原代鼻咽上皮细胞中 EBV 的感染。在端粒酶永生化鼻咽上皮细胞系 NP460hTert 中实现了 EBV 的稳定感染。监测了该 EBV 感染鼻咽上皮细胞系中 EBV 编码基因的表达模式及其长期传代的生物学特性。EBV 感染的鼻咽上皮细胞获得了非锚定依赖性生长,并在长期传代中表现出侵袭性生长特性。这种 EBV 感染的鼻咽上皮细胞模型的一个显著特征是其在生长因子和营养饥饿下的存活能力增强。这一点从 EBV 感染细胞在营养饥饿下与对照细胞相比,凋亡标志物的激活受到抑制,pAkt 的持续激活得到证实。对 EBV 感染的 NP460hTert 细胞在营养和生长因子剥夺下的细胞因子谱进行检测,发现 MCP-1 和 GRO-α的表达上调。建立稳定的鼻咽癌前上皮细胞 EBV 感染模型将有助于研究 EBV 在 NPC 发展中的致病作用。