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用非转化性P3HR-1 EBV超感染非产生细胞后转化性EBV的恢复。

Recovery of transforming EBV from non-producer cells after superinfection with non-transforming P3HR-1 EBV.

作者信息

Fresen K O, Cho M S, zur Hausen H

出版信息

Int J Cancer. 1978 Oct 15;22(4):378-83. doi: 10.1002/ijc.2910220403.

Abstract

Cells of the Raji and NC37 lines can be induced by chemical inducers, such as BrdUrd and IdUrd, or the tumor-promoter TPA to EA-expression only, but do not reveal any VCA synthesis. After superinfection by nontransforming P3HR-1 EBV, however, a varying percentage of the cell population shows VCA synthesis and releases infectious viral particles. The recovered virus differs biologically from P3HR-1 EBV since it transforms human umbilical cord blood lymphocytes into EBNA-positive lymphoblastoid cell lines. Cells of these established lines are susceptible to renewed infection by P3HR-1 EBV which results in EA induction and VCA synthesis. Only cells of one line, NC37-R1, spontaneously produce VCA and EBV particles, which reveal transforming properties and do not induce EA upon superinfection of Raji cells. Infection of P3HR-1 EBV-converted BJA-B cells also leads to EA and VCA induction and the release of viral particles. In contrast to particles recovered from Raji and NC37 cells, no transforming activity was detectable in these virus preparations. According to these data, we propose that viral genomes persisting within Raji and NC37 cells are defective and become complemented by the superinfecting P3HR-1 virus.

摘要

拉吉(Raji)细胞系和NC37细胞系的细胞可被化学诱导剂(如溴脱氧尿苷和碘脱氧尿苷)或肿瘤促进剂佛波酯(TPA)诱导,仅表达早期抗原(EA),但不显示任何病毒衣壳抗原(VCA)的合成。然而,在用非转化性P3HR-1型EB病毒(EBV)超感染后,不同比例的细胞群体显示出VCA的合成并释放出有感染性的病毒颗粒。回收的病毒在生物学特性上与P3HR-1型EBV不同,因为它能将人脐带血淋巴细胞转化为EB病毒核抗原(EBNA)阳性的淋巴母细胞系。这些已建立细胞系的细胞易受P3HR-1型EBV的再次感染,这会导致EA的诱导和VCA的合成。只有一个细胞系NC37-R1的细胞能自发产生VCA和EBV颗粒,这些颗粒具有转化特性,并且在超感染拉吉细胞时不会诱导EA。用P3HR-1型EBV转化的BJA-B细胞的感染也会导致EA和VCA的诱导以及病毒颗粒的释放。与从拉吉细胞和NC37细胞中回收的颗粒相比,在这些病毒制剂中未检测到转化活性。根据这些数据,我们提出,持续存在于拉吉细胞和NC37细胞内的病毒基因组是有缺陷的,并由超感染的P3HR-1病毒进行互补。

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