Takada K
Hokkaido Igaku Zasshi. 1980 Sep;55(5):447-70.
A simple method for simultaneous comparative observations of immunofluorescence, cellular morphology and autoradiography has been developed, and this method was applied to investigate the early transformation events of human cord blood lymphocytes by Epstein-Barr virus (EBV). The results indicated that transformation occurred sequentially from EBV-determined nuclear antigen (EBNA) synthesis, to blastogenesis, to DNA synthesis, and consistently resulted in unlimited growth of the antigen-positive lymphoblasts. EBNA synthesis was not hampered in the presence of Ara C, but was significantly inhibited by a short-term exposure to cycloheximide immediately after EBV infection. The response of leukemic cells to EBV was further studied. Only leukemic lymphocytes with B-cell markers showed susceptibility to EBV, in close connection with the presence of complement receptor. In contrast to EBV infection of normal B-lymphocytes, EBNA synthesis in three chronic lymphocytic leukemia (CLL) preparations was not followed by either blastogenesis or DNA synthesis and the infected cells shortly resulted in cell degeneration. In case of acute lymphocytic leukemia (ALL), EBNA-positive cells were highly evident and grew rapidly for up to 9 days. The cell proliferation, however, was temporary and death resulted in about 2 weeks. No significant synthesis of EBV-related early antigens and viral capsid antigen was noted in any of the infected culture throughout the incubation period.
已开发出一种用于同时进行免疫荧光、细胞形态学和放射自显影比较观察的简单方法,并将该方法应用于研究爱泼斯坦-巴尔病毒(EBV)对人脐血淋巴细胞的早期转化事件。结果表明,转化过程依次从EBV决定的核抗原(EBNA)合成开始,到细胞增殖,再到DNA合成,并始终导致抗原阳性淋巴母细胞的无限生长。在阿糖胞苷存在的情况下,EBNA合成不受阻碍,但在EBV感染后立即短期暴露于环己酰亚胺会受到显著抑制。对白血病细胞对EBV的反应进行了进一步研究。只有具有B细胞标志物的白血病淋巴细胞显示出对EBV的敏感性,这与补体受体的存在密切相关。与正常B淋巴细胞的EBV感染不同,三种慢性淋巴细胞白血病(CLL)制剂中的EBNA合成之后既没有细胞增殖也没有DNA合成,并且被感染的细胞很快导致细胞变性。在急性淋巴细胞白血病(ALL)的情况下,EBNA阳性细胞非常明显,并快速生长长达9天。然而,细胞增殖是暂时的,约2周后导致死亡。在整个培养期间,在任何感染培养物中均未观察到EBV相关早期抗原和病毒衣壳抗原的显著合成。