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氨基酸类似物L-刀豆氨酸对爱泼斯坦-巴尔病毒诱导的差异抑制作用

Differential inhibition of Epstein-Barr virus induction by the amino acid analogue, L-canavanine.

作者信息

Yamamoto N, Mueller-Lantzsch N, zur Hausen H

出版信息

Int J Cancer. 1980 Apr 15;25(4):439-43. doi: 10.1002/ijc.2910250403.

Abstract

The effect of an amino acid analogue, L-canavanine, on the synthesis of Epstein-Barr virus (EBV) antigens was investigated in lymphoblastoid cells. The analysis revealed that after infection of BJAB and NC-37 cells with P3HR-I EBV synthesis of early antigen (EA) was not affected by canavanine in concentrations up to 8.4 mM. The synthesis of EBV-determined nuclear antigen (EBNA) and of viral capsid antigen (VCA) was significantly inhibited at concentrations higher than 2.8 mM. Spontaneous induction of EA in P3HR-I cells was not affected by canavanine. On the other hand, EA induction by the tumor promoter TPA resulted in some viral antigen induction depending on the time period of TPA exposure. Pretreatment of the cells overnight with canavanine followed by washing and addition of the tumor promoter did not suppress EA induction by TPA. These data support the concept that EA induction by superinfection follows a different pathway from antigen induction by chemical inducers.

摘要

在淋巴母细胞中研究了一种氨基酸类似物L-刀豆氨酸对爱泼斯坦-巴尔病毒(EBV)抗原合成的影响。分析表明,用P3HR-I EBV感染BJAB和NC-37细胞后,浓度高达8.4 mM的刀豆氨酸对早期抗原(EA)的合成没有影响。当浓度高于2.8 mM时,EBV决定的核抗原(EBNA)和病毒衣壳抗原(VCA)的合成受到显著抑制。P3HR-I细胞中EA的自发诱导不受刀豆氨酸的影响。另一方面,肿瘤启动子TPA诱导EA会导致一些病毒抗原的诱导,这取决于TPA暴露的时间段。用刀豆氨酸将细胞预处理过夜,然后洗涤并加入肿瘤启动子,并不会抑制TPA诱导的EA。这些数据支持这样一种观点,即重叠感染诱导EA遵循与化学诱导剂诱导抗原不同的途径。

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