Pauls Eduardo, Senserrich Jordi, Clotet Bonaventura, Esté Jose A
Retrovirology Laboratroy irsiCaixa, Hospital Universitari Germans Trias i Pujol, Universitat Autònoma de Barcelona, Ctra. Del Canyet s/n, Badalona, Barcelona 08916, Spain.
J Leukoc Biol. 2006 Sep;80(3):659-67. doi: 10.1189/jlb.0306189. Epub 2006 Jul 14.
p53 expression and activation have been associated to faster human immunodeficiency virus (HIV) disease progression, most probably by inducing CD4+ T cell death but also through its cooperative effect in the control of viral gene transcription by viral regulatory proteins. Here, we show that RNA interference of p53 in HIV-1 reporter (HeLa P4-R5 MAGI) and lymphoid (SupT1) cell lines blocked HIV-1 and Tat-induced transcription from the HIV-1 promoter and HIV-1 replication in acutely infected cells, suggesting a cooperative role of p53 in HIV-1 transcription. Contrary to SupT1 cells, which encode several mutations on the p53 DNA binding domain, death of HIV-1-induced syncytia was reduced in cocultures of HeLa P4-R5 MAGI with persistently infected HIV-1 cells. To our knowledge, this is the first demonstration of the effect of the loss of function of p53 in HIV-1 replication, which is independent on its classical DNA binding activity. Our results suggest two independent roles for p53 in HIV-1 infection: cooperation in HIV long-terminal repeat transcription and virus-induced cell death.
p53的表达和激活与人类免疫缺陷病毒(HIV)疾病的快速进展有关,最有可能是通过诱导CD4+ T细胞死亡,也可能是通过其在病毒调节蛋白控制病毒基因转录中的协同作用。在此,我们表明,在HIV-1报告细胞系(HeLa P4-R5 MAGI)和淋巴细胞系(SupT1)中对p53进行RNA干扰,可阻断HIV-1和Tat诱导的HIV-1启动子转录以及急性感染细胞中的HIV-1复制,这表明p53在HIV-1转录中具有协同作用。与在p53 DNA结合域编码多个突变的SupT1细胞相反,HeLa P4-R5 MAGI与持续感染HIV-1的细胞共培养时,HIV-1诱导的多核巨细胞死亡减少。据我们所知,这是首次证明p53功能丧失对HIV-1复制的影响,且该影响独立于其经典的DNA结合活性。我们的结果表明p53在HIV-1感染中有两个独立作用:在HIV长末端重复序列转录中的协同作用以及病毒诱导的细胞死亡。