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细胞表面免疫球蛋白的交联可诱导伯基特淋巴瘤细胞系中的爱泼斯坦-巴尔病毒。

Cross-linking of cell surface immunoglobulins induces Epstein-Barr virus in Burkitt lymphoma lines.

作者信息

Takada K

出版信息

Int J Cancer. 1984 Jan 15;33(1):27-32. doi: 10.1002/ijc.2910330106.

Abstract

Anti-human immunoglobulin (Ig) antibodies with single-chain specificities induced Epstein-Barr virus (EBV) in various Burkitt lymphoma lines when the corresponding Ig chain was expressed on the cell surface. The F(ab')2 fragments of IgG antibody were as potent as intact Ig, while the Fab and Fc fragments gave no induction, indicating that cross-linking of surface Ig was required for the induction. Simultaneously with EBV induction, anti-Ig inhibited the uptake of 3H-thymidine. This inhibition was also seen in EBV-genome-negative Burkitt lymphoma lines. In contrast, no effect on virus induction and cell growth was noted in lymphoblastoid lines of non-neoplastic origin. The possible relationship between cell differentiation and latency of EBV-carrier state is discussed.

摘要

当相应的免疫球蛋白(Ig)链在细胞表面表达时,具有单链特异性的抗人Ig抗体在多种伯基特淋巴瘤细胞系中诱导了爱泼斯坦-巴尔病毒(EBV)。IgG抗体的F(ab')2片段与完整Ig一样有效,而Fab和Fc片段则无诱导作用,这表明表面Ig的交联是诱导所必需的。在诱导EBV的同时,抗Ig抑制了3H-胸腺嘧啶核苷的摄取。这种抑制在EBV基因组阴性的伯基特淋巴瘤细胞系中也可见到。相比之下,在非肿瘤来源的淋巴母细胞系中未观察到对病毒诱导和细胞生长的影响。本文讨论了细胞分化与EBV携带状态潜伏期之间的可能关系。

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