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作 者:江培洲[1] 沈新明[1] 黄华[1] 姚开泰[1]
机构地区:[1]第一军医大学肿瘤研究所,广东广州510515
出 处:《第一军医大学学报》2002年第11期970-973,共4页Journal of First Military Medical University
基 金:国家863项目(2001AA216101);广东省"十五"攻关项目(A1080201)
摘 要:目的探讨EB病毒感染上皮细胞的机制。方法大规模培养绒猴淋巴细胞B958系,从中提取并浓缩EB病毒,用胎儿脐带血淋巴细胞滴定后,以高浓度EB病毒感染人永生化上皮细胞Hacat系。提取Hacat细胞基因组DNA,PCR扩增EB病毒基因组特异性核酸序列BamHIw片断,Southernblotting及原位杂交验证感染结果。结果PCR、Southerblotting及原位杂交结果证实高浓度EB病毒能够感染Hacat细胞,但是感染率非常低。结论EBV对上皮细胞存在CR2或多聚IgA受体介导之外的未知感染途径。Objective To study the mechanism by which Epstein-Barr (E B) virus infects human epithelial cells. Methods Large-scale culture of marmoset l ymphocytes B958 was carried out to extract and condense EB virus therein. Titra ted by lym-phocytes from fetal umbilical blood, the EB virus of high concentrati on was used to infect immortalized human epithelial cell line Hacat, followed b y genomic DNA extraction from the Hacat cells and amplification of the special D NA sequence Bam HIw fragments of EBV genomic DNA by PCR. Southern blotting and in situ hybridization were employed to confirm the result of PCR. Results The r esults of PCR, Southern blotting and in situ hybridization all indicated that hi gh-concentration EBV could infect Hacat cell line, but the rate of infection wa s rather low. Conclusion There is an unknown pathway of infection for EBV entry into the epithelial cells other than the mediation by CR2 or pIgR.
关 键 词:EB病毒 上皮细胞 病毒学 鼻咽肿瘤 病因学 胎盘
分 类 号:R739.63[医药卫生—肿瘤] R730.231.3[医药卫生—临床医学]
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