Cobos Jiménez Viviana, Martinez Fernando O, Booiman Thijs, van Dort Karel A, van de Klundert Maarten A A, Gordon Siamon, Geijtenbeek Teunis B H, Kootstra Neeltje A
Department of Experimental Immunology, Sanquin Research, Landsteiner Laboratory, and Center for Infectious Diseases and Immunity Amsterdam (CINIMA), Academic Medical Center of the University of Amsterdam, Amsterdam 1105AZ, The Netherlands.
Kennedy Rheumatology Institute, University of Oxford, Oxford OX3 7LD, United Kingdom.
Virology. 2015 Dec;486:94-104. doi: 10.1016/j.virol.2015.09.007. Epub 2015 Sep 29.
HIV-1 exploits the cellular machinery for replication and therefore several interactions with cellular factors take place, some of which are yet unknown. We identified GTPase-activating protein-(SH3 domain)-binding protein 1 (G3BP1) as a cellular factor that restricts HIV-1, by analyzing transcriptome profiles of in vitro-cytokine-activated macrophages that are non-permissive to HIV-1 replication. Silencing of G3BP1 by RNA interference resulted in increased HIV-1 replication in primary T-cells and macrophages, but did not affect replication of other retroviruses. G3BP1 specifically interacted with HIV-1 RNA in the cytoplasm, suggesting that it sequesters viral transcripts, thus preventing translation or packaging. G3BP1 was highly expressed in resting naïve or memory T-cells from healthy donors and HIV-1 infected patients, but significantly lower in IL-2-activated T-cells. These results strongly suggest that G3BP1 captures HIV-1 RNA transcripts and thereby restricts mRNA translation, viral protein production and virus particle formation.
HIV-1利用细胞机制进行复制,因此会与细胞因子发生多种相互作用,其中一些相互作用尚不清楚。通过分析对HIV-1复制不敏感的体外细胞因子激活的巨噬细胞的转录组图谱,我们鉴定出GTP酶激活蛋白(SH3结构域)结合蛋白1(G3BP1)是一种限制HIV-1的细胞因子。通过RNA干扰使G3BP1沉默导致原代T细胞和巨噬细胞中HIV-1复制增加,但不影响其他逆转录病毒的复制。G3BP1在细胞质中与HIV-1 RNA特异性相互作用,表明它隔离病毒转录本,从而阻止翻译或包装。G3BP1在健康供体和HIV-1感染患者的静息初始或记忆T细胞中高度表达,但在IL-2激活的T细胞中显著降低。这些结果强烈表明,G3BP1捕获HIV-1 RNA转录本,从而限制mRNA翻译、病毒蛋白产生和病毒颗粒形成。