Tang Yunlian, Lu Suli, Gan Xiaoning, Liu Fang, Zhang Yang, Luo Chunyan, Pan Yuxia, Hong Li, Gan Ruliang
Cancer Research Institute, College of Medicine, University of South China, Hengyang, Hunan 421001, P.R. China.
College of Medicine, University of South China, Hengyang, Hunan 421001, P.R. China.
Oncol Rep. 2016 Feb;35(2):905-11. doi: 10.3892/or.2015.4401. Epub 2015 Nov 5.
Transplantation of peripheral blood lymphocytes (PBLs) from healthy humans with latent Epstein-Barr virus (EBV) infection into severe combined immunodeficiency (SCID) mice results in development of EBV-associated human B-cell lymphoma. However, the expression of EBV genes in relation to lymphoma development has not been reported. We investigated latent membrane protein (LMP) and EBV nuclear antigen (EBNA) gene expression in PBLs from EBV-positive blood donors and induced-lymphoma cells from SCID mice to elucidate the functions and effects of the EBV genome in the occurrence and development of lymphoma. PBLs were isolated from 9 healthy blood donors and transplanted into SCID mice. Gene expression levels of LMP-1, LMP-2A, and LMP-2B and EBNA-1, EBNA-2, EBNA-3A, EBNA-3B, EBNA-3C and EBNA-LP were monitored by real-time quantitative-polymerase chain reaction (qRT-PCR) in cells from nine EBV-induced lymphomas and in matched lymphocytes from healthy subjects. LMP-1, EBNA-1 and EBNA-2 protein levels were detected by western blotting. As a result, LMP-1, LMP-2A and LMP-2B mRNA levels were upregulated 256-, 38- and 331-fold, respectively, in the EBV-induced lymphoma cells compared with the controls, while EBNA-1 and EBNA-3A mRNA levels were upregulated 1157- and 1154-fold, respectively. EBNA-2, EBNA-3B, EBNA-3C and EBNA-LP mRNAs were detected in lymphoma cells, but not in lymphocytes from EBV-positive blood donors. LMP-1 and EBNA-2 proteins were not expressed in lymphocytes from EBV-positive blood donors, according to western blotting. Weak EBNA-1 expression was observed in lymphocytes from blood donors with latent EBV infection, while LMP-1, EBNA-1 and EBNA-2 protein levels were significantly upregulated in EBV-induced lymphoma cells, consistent with mRNA expression levels detected by qRT-PCR. In conclusion, LMP-1, LMP-2A, LMP-2B, EBNA-1 and EBNA-3A were upregulated in EBV-induced lymphoma cells, while EBNA-2, EBNA-3B, EBNA-3C and EBNA-LP were absent in lymphocytes from humans with latent EBV infection, but were positively expressed in EBV-induced lymphoma cells.
将潜伏性感染爱泼斯坦-巴尔病毒(EBV)的健康人的外周血淋巴细胞(PBLs)移植到重症联合免疫缺陷(SCID)小鼠体内会导致EBV相关的人类B细胞淋巴瘤的发生。然而,尚未有关于EBV基因表达与淋巴瘤发生关系的报道。我们研究了EBV阳性献血者的PBLs以及SCID小鼠诱导淋巴瘤细胞中潜伏膜蛋白(LMP)和EBV核抗原(EBNA)基因的表达,以阐明EBV基因组在淋巴瘤发生发展中的功能和作用。从9名健康献血者中分离出PBLs并移植到SCID小鼠体内。通过实时定量聚合酶链反应(qRT-PCR)监测来自9例EBV诱导淋巴瘤的细胞以及健康受试者匹配淋巴细胞中LMP-1、LMP-2A、LMP-2B和EBNA-1、EBNA-2、EBNA-3A、EBNA-3B、EBNA-3C和EBNA-LP的基因表达水平。通过蛋白质印迹法检测LMP-1、EBNA-1和EBNA-2蛋白水平。结果显示,与对照组相比,EBV诱导淋巴瘤细胞中LMP-1、LMP-2A和LMP-2B的mRNA水平分别上调了256倍、38倍和331倍,而EBNA-1和EBNA-3A的mRNA水平分别上调了1157倍和1154倍。在淋巴瘤细胞中检测到了EBNA-2、EBNA-3B、EBNA-3C和EBNA-LP的mRNA,但在EBV阳性献血者的淋巴细胞中未检测到。根据蛋白质印迹法,EBV阳性献血者的淋巴细胞中未表达LMP-1和EBNA-2蛋白。在潜伏性感染EBV的献血者的淋巴细胞中观察到EBNA-1表达较弱,而在EBV诱导的淋巴瘤细胞中LMP-1、EBNA-1和EBNA-2蛋白水平显著上调,这与qRT-PCR检测到的mRNA表达水平一致。总之,在EBV诱导的淋巴瘤细胞中LMP-1、LMP-2A、LMP-2B、EBNA-1和EBNA-3A上调,而在潜伏性感染EBV的人的淋巴细胞中不存在EBNA-2、EBNA-3B、EBNA-3C和EBNA-LP,但在EBV诱导的淋巴瘤细胞中呈阳性表达。