Jiang Wei-Min, Zhang Xin-Yun, Zhang Yun-Zhi, Liu Li, Lu Hong-Zhou
Huashan Hospital Affiliated to Fudan University Shanghai, China.
Department of Infectious Diseases, Shanghai Public Health Clinical Center, Fudan University Shanghai, China.
Int J Clin Exp Pathol. 2014 Apr 15;7(5):2229-37. eCollection 2014.
Drug resistance remains a great challenge in HIV/AIDS treatment despite the recent advances in novel therapeutics. It may be a good strategy to develop drugs targeting the essential host factors to decrease the risk of drug resistance. Previous studies suggested that so many host kinases play roles in HIV life cycles. More importantly, many kinase genes are drugable targets, therefore, it is vital to figure out host kinases responsible for HIV-1 infection and replication to provide novel therapeutic regimens and to deepen our understanding to HIV-host interaction. In present work, a high throughput RNAi screen with a shRNA library against 474 kinases was applied to HEK293T cells stably expressed a HIV-1 LTR (long terminal repeat)-driven reporter plasmid. Four genes, AK1, EphB2, PRKACB and CDK5R2, were found to specifically suppress the HIV-1 LTR activity following effective knockdown. Furthermore, overexpression of AK1 and PRKACB upregulated the HIV-1 LTR activity. Therefore, AK1 and PRKACB are in positive control of HIV-1 activity. DNA microarray analysis demonstrated that overlapped genes between AK1-silenced and PRKACB-silenced cells were mainly enriched in several amino acid biosynthesis pathways, TGF-β signaling and p53 signaling pathways. These alterations may repress the viral infection by the downregulation of ERK1/2, p38MAPK and NFκB signaling pathways. Collectively, our work uncovers several host kinases involving the HIV-1 infection and may provide potential therapeutic targets for AIDS treatment in future.
尽管新型疗法最近取得了进展,但耐药性仍然是艾滋病毒/艾滋病治疗中的一个巨大挑战。开发针对宿主必需因子的药物可能是降低耐药风险的一个好策略。先前的研究表明,许多宿主激酶在艾滋病毒的生命周期中发挥作用。更重要的是,许多激酶基因是可药物作用的靶点,因此,确定负责艾滋病毒-1感染和复制的宿主激酶对于提供新的治疗方案以及加深我们对艾滋病毒与宿主相互作用的理解至关重要。在目前的工作中,我们将针对474种激酶的shRNA文库进行的高通量RNAi筛选应用于稳定表达艾滋病毒-1长末端重复序列(LTR)驱动的报告质粒的人胚肾293T细胞。在有效敲低后,发现四个基因AK1、EphB2、PRKACB和CDK5R2特异性抑制艾滋病毒-1 LTR活性。此外,AK1和PRKACB的过表达上调了艾滋病毒-1 LTR活性。因此,AK1和PRKACB对艾滋病毒-1活性起正调控作用。DNA微阵列分析表明,AK1沉默细胞和PRKACB沉默细胞之间的重叠基因主要富集在几个氨基酸生物合成途径、TGF-β信号通路和p53信号通路中。这些改变可能通过下调ERK1/2、p38MAPK和NFκB信号通路来抑制病毒感染。总的来说,我们的工作揭示了几种参与艾滋病毒-1感染的宿主激酶,并可能为未来的艾滋病治疗提供潜在的治疗靶点。