Benson R E, Sanfridson A, Ottinger J S, Doyle C, Cullen B R
Howard Hughes Medical Institute, Duke University Medical Center, Durham, North Carolina 27710.
J Exp Med. 1993 Jun 1;177(6):1561-6. doi: 10.1084/jem.177.6.1561.
The nef gene product encoded by the mac239 proviral clone of simian immunodeficiency virus (SIV) markedly enhances viral replication and pathogenesis in vivo. We have used this biologically active nef isolate to examine the phenotype of Nef in retrovirally transduced human T cells in culture. SIV Nef is shown to dramatically inhibit cell-surface expression of the CD4 glycoprotein without significantly affecting the total steady-state level of cellular CD4. This downregulation of the cell-surface CD4 receptor for human immunodeficiency virus type 1 (HIV-1) infection correlated with the acquisition of resistance to superinfection by HIV-1. However, SIV Nef did not affect the level of gene expression directed by the HIV-1 long terminal repeat. It is hypothesized that downregulation of cell-surface CD4 by Nef facilitates the efficient release of infectious progeny virions and, hence, viral spread in vivo.
猿猴免疫缺陷病毒(SIV)的mac239前病毒克隆编码的nef基因产物在体内显著增强病毒复制和致病作用。我们已使用这种具有生物活性的nef分离株来检测逆转录病毒转导的培养人T细胞中Nef的表型。结果显示,SIV Nef可显著抑制CD4糖蛋白的细胞表面表达,而对细胞CD4的总稳态水平无明显影响。这种针对人类免疫缺陷病毒1型(HIV-1)感染的细胞表面CD4受体的下调与获得对HIV-1超感染的抗性相关。然而,SIV Nef并不影响HIV-1长末端重复序列指导的基因表达水平。据推测,Nef对细胞表面CD4的下调促进了感染性子代病毒颗粒的有效释放,从而促进了病毒在体内的传播。