Menet A, Speth C, Larcher C, Prodinger W M, Schwendinger M G, Chan P, Jäger M, Schwarzmann F, Recheis H, Fontaine M, Dierich M P
INSERM U519, 76000 Rouen, France.
J Virol. 1999 Sep;73(9):7722-33. doi: 10.1128/JVI.73.9.7722-7733.1999.
Epstein-Barr virus (EBV) is implicated in different central nervous system syndromes. The major cellular receptor for EBV, complement receptor type 2 (CR2) (CD21), is expressed by different astrocyte cell lines and human fetal astrocytes, suggesting their susceptibility to EBV infection. We demonstrated the infection of two astrocyte cell lines, T98 and CB193, at low levels. As infection was mediated by CR2, we used two stable CR2 transfectant astrocyte cell lines (T98CR2 and CB193CR2) to achieve a more efficient infection. We have monitored EBV gene expression for 2 months and observed the transient infection of T98 and T98CR2 cells and persistent infection of CB193 and CB193CR2 cells. The detection of BZLF1, BALF2, and BcLF1 mRNA expression suggests that the lytic cycle is initiated at early time points postinfection. At later time points the pattern of mRNA expressed (EBER1, EBNA1, EBNA2, and LMP1) differs from latency type III in the absence of LMP2A transcription and in the expression of BALF2 and BcLF1 but not BZLF1. A reactivation of the lytic cycle was achieved in CB193CR2 cells by the addition of phorbol esters. These studies identify astrocyte cell lines as targets for EBV infection and suggest that this infection might play a role in the pathology of EBV in the brain.
爱泼斯坦-巴尔病毒(EBV)与不同的中枢神经系统综合征有关。EBV的主要细胞受体,即2型补体受体(CR2)(CD21),在不同的星形胶质细胞系和人胎儿星形胶质细胞中表达,表明它们易受EBV感染。我们证明了两种星形胶质细胞系T98和CB193能被低水平感染。由于感染是由CR2介导的,我们使用了两种稳定转染CR2的星形胶质细胞系(T98CR2和CB193CR2)以实现更有效的感染。我们监测了EBV基因表达2个月,观察到T98和T98CR2细胞的短暂感染以及CB193和CB193CR2细胞的持续感染。BZLF1、BALF2和BcLF1 mRNA表达的检测表明,裂解周期在感染后的早期时间点开始。在随后的时间点,所表达的mRNA模式(EBER1、EBNA1、EBNA2和LMP1)与潜伏III型不同,表现为缺乏LMP2A转录以及BALF2和BcLF1的表达,但不包括BZLF1。通过添加佛波酯在CB193CR2细胞中实现了裂解周期的重新激活。这些研究确定星形胶质细胞系是EBV感染的靶标,并表明这种感染可能在EBV在脑部的病理学中起作用。