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鼠嗜亲性莫洛尼逆转录病毒载体与人类细胞的抗体介导结合可实现内化,但无法建立前病毒状态。

Antibody-mediated binding of a murine ecotropic Moloney retroviral vector to human cells allows internalization but not the establishment of the proviral state.

作者信息

Goud B, Legrain P, Buttin G

机构信息

Département d'Immunologie, Institut Pasteur, Paris, France.

出版信息

Virology. 1988 Mar;163(1):251-4. doi: 10.1016/0042-6822(88)90261-9.

Abstract

We have attempted to introduce a neomycin-resistance gene, recombined in a murine (ecotropic) Moloney retrovirus, into HEp2 human cells which are resistant to infection by this retrovirus. To allow the binding of the retroviral vector on HEp2 cells, we have tested several antibody constructions between two monoclonal antibodies, one (mAb 5E9) directed against the human transferrin receptor and the other (mAb 615) directed against the gp70 envelope viral protein. The crosslinking of mAbs 5E9 and 615 by a sheep anti-murine kappa light chain antibody allowed the binding of virus on HEp2 cells. After incubation at 37 degrees, virus was internalized by HEp2 cells. However, no neomycin-resistant colonies of HEp2 cells have been obtained under various conditions. Our results suggest that binding and internalization of a retrovirus are not sufficient for establishment of the proviral state in cells which do not express a specific receptor.

摘要

我们试图将一个重组于鼠(嗜亲性)莫洛尼逆转录病毒中的新霉素抗性基因导入对该逆转录病毒感染具有抗性的HEp2人细胞。为使逆转录病毒载体能够结合到HEp2细胞上,我们测试了两种单克隆抗体之间的几种抗体构建体,一种(单克隆抗体5E9)针对人转铁蛋白受体,另一种(单克隆抗体615)针对gp70包膜病毒蛋白。用羊抗鼠κ轻链抗体使单克隆抗体5E9和615交联,从而使病毒能够结合到HEp2细胞上。在37℃孵育后,病毒被HEp2细胞内化。然而,在各种条件下均未获得HEp2细胞的新霉素抗性菌落。我们的结果表明,逆转录病毒的结合和内化不足以在不表达特定受体的细胞中建立前病毒状态。

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