Takada K, Osato T
Intervirology. 1979;11(1):30-9. doi: 10.1159/000149009.
A B-cell population of human cord blood lymphocytes was exposed to the B95-8 strain of Epstein-Barr virus (EBV), and simultaneous observations of immunofluorescence, cellular morphology and autoradiography were carried out in each individual cell. It was evident that EBV-determined nuclear antigen (EBNA) synthesis occurred prior to blastogenic response and DNA synthesis. EBNA-positive cells could be observed as early as 12 h after infection and reached a maximum of 17% at 24 h, followed by a plateau for a subsequent 12 h. The positive cells were seen exclusively as morphologically normal lymphocytes until 18 h; at 24 h, blastogenesis became evident, without cell division. DNA synthesis was detected at 36 h in EBNA-positive blast cells, after which these cells increased rapidly. EBNA synthesis was similarly evident in the presence of cytosine arabinoside, but was significantly inhibited by a short-term exposure to cycloheximide immediately after infection. These findings suggest that the early events in EBV-induced transformation of human lymphocytes occur sequentially from EBNA synthesis, to blastogenesis, to DNA synthesis and that the crucial step of such transformation is probably involved in protein synthesis occurring in the very early stage of EBV infection.
将人脐带血淋巴细胞的B细胞群体暴露于爱泼斯坦-巴尔病毒(EBV)的B95-8株,并对每个细胞同时进行免疫荧光、细胞形态学和放射自显影观察。很明显,EBV决定的核抗原(EBNA)合成发生在增殖反应和DNA合成之前。感染后12小时即可观察到EBNA阳性细胞,24小时时达到最大值17%,随后在接下来的12小时保持稳定。直到18小时,阳性细胞仅表现为形态正常的淋巴细胞;24小时时,增殖变得明显,但无细胞分裂。在EBNA阳性的母细胞中36小时检测到DNA合成,此后这些细胞迅速增加。在存在阿糖胞苷的情况下,EBNA合成同样明显,但在感染后立即短期暴露于环己酰亚胺会显著抑制EBNA合成。这些发现表明,EBV诱导人淋巴细胞转化的早期事件从EBNA合成开始,依次到增殖,再到DNA合成,并且这种转化的关键步骤可能涉及EBV感染早期阶段发生的蛋白质合成。