Division of Medical Science, Centre for Oncology and Molecular Medicine, University of Dundee, Ninewells Hospital, Dundee, Scotland, United Kingdom.
J Virol. 2012 Aug;86(16):8452-60. doi: 10.1128/JVI.07143-11. Epub 2012 May 30.
Previous studies have described the role of p53 isoforms, including p53β and Δ133p53α, in the modulation of the activity of full-length p53, which regulates cell fate. In the context of influenza virus infection, an interplay between influenza viruses and p53 has been described, with p53 being involved in the antiviral response. However, the role of physiological p53 isoforms has never been explored in this context. Here, we demonstrate that p53 isoforms play a role in influenza A virus infection by using silencing and transient expression strategies in human lung epithelial cells. In addition, with the help of a panel of different influenza viruses from different subtypes, we also show that infection differentially regulates the expressions of p53β and Δ133p53α. Altogether, our results highlight the role of p53 isoforms in the viral cycle of influenza A viruses, with p53β and Δ133p53α acting as regulators of viral production in a p53-dependent manner.
先前的研究描述了 p53 异构体(包括 p53β 和 Δ133p53α)在调节全长 p53 活性方面的作用,全长 p53 调节细胞命运。在流感病毒感染的背景下,已经描述了流感病毒与 p53 之间的相互作用,p53 参与抗病毒反应。然而,在这种情况下,生理 p53 异构体的作用从未被探索过。在这里,我们通过在人肺上皮细胞中使用沉默和瞬时表达策略,证明了 p53 异构体在甲型流感病毒感染中发挥作用。此外,借助来自不同亚型的不同流感病毒的面板,我们还表明感染以不同的方式调节 p53β 和 Δ133p53α 的表达。总之,我们的研究结果强调了 p53 异构体在甲型流感病毒病毒周期中的作用,p53β 和 Δ133p53α 以 p53 依赖性方式作为病毒产生的调节剂。