Re F, Braaten D, Franke E K, Luban J
Department of Microbiology, Columbia University College of Physicians and Surgeons, New York, New YOrk 10032, USA.
J Virol. 1995 Nov;69(11):6859-64. doi: 10.1128/JVI.69.11.6859-6864.1995.
Human immunodeficiency virus type 1 (HIV-1) vpr inhibits the replication of tumor cell lines and peripheral blood mononuclear cells. Here it is demonstrated that expression of vpr, either in the context of a provirus or from an independent genetic element, induces a discrete cell cycle arrest, with cells containing 4N DNA. Low cyclin B-associated kinase activity, as well as the status of p34cdc2 and cdc25C phosphorylation, indicates that the cascade of reactions which drives the cell into mitosis has not been initiated. The phosphatase inhibitor okadaic acid releases the block, suggesting that Vpr perturbs upstream regulatorsof the G2-M transition. These studies demonstrate that HIV-1 vpr has profound effects on the cellular factors which control entry into mitosis and indicate vpr's potential contribution to the cellular pathology associated with HIV-1 infection.
1型人类免疫缺陷病毒(HIV-1)的Vpr蛋白可抑制肿瘤细胞系和外周血单核细胞的复制。本文证明,无论是在原病毒的背景下还是来自独立的遗传元件,Vpr蛋白的表达都会诱导细胞周期出现离散性停滞,使细胞含有4N DNA。细胞周期蛋白B相关激酶活性较低,以及p34cdc2和cdc25C的磷酸化状态,表明驱动细胞进入有丝分裂的反应级联尚未启动。磷酸酶抑制剂冈田酸可解除这种阻滞,这表明Vpr蛋白扰乱了G2-M转换的上游调节因子。这些研究表明,HIV-1的Vpr蛋白对控制进入有丝分裂的细胞因子有深远影响,并表明Vpr蛋白对与HIV-1感染相关的细胞病理学有潜在贡献。