Department of Molecular and Microbiology, George Mason University, Manassas, Virginia, USA.
PLoS Pathog. 2009 Dec;5(12):e1000520. doi: 10.1371/journal.ppat.1000520. Epub 2009 Dec 24.
Binding of the HIV-1 envelope to its chemokine coreceptors mediates two major biological events: membrane fusion and signaling transduction. The fusion process has been well studied, yet the role of chemokine coreceptor signaling in viral infection has remained elusive through the past decade. With the recent demonstration of the signaling requirement for HIV latent infection of resting CD4 T cells, the issue of coreceptor signaling needs to be thoroughly revisited. It is likely that virus-mediated signaling events may facilitate infection in various immunologic settings in vivo where cellular conditions need to be primed; in other words, HIV may exploit the chemokine signaling network shared among immune cells to gain access to downstream cellular components, which can then serve as effective tools to break cellular barriers. This virus-hijacked aberrant signaling process may in turn facilitate pathogenesis. In this review, we summarize past and present studies on HIV coreceptor signaling. We also discuss possible roles of coreceptor signaling in facilitating viral infection and pathogenesis.
HIV-1 包膜与趋化因子核心受体的结合介导了两个主要的生物学事件:膜融合和信号转导。融合过程已经得到了很好的研究,但在过去的十年中,趋化因子核心受体信号在病毒感染中的作用仍然难以捉摸。随着最近证明了 HIV 潜伏感染静止 CD4 T 细胞需要信号转导,核心受体信号的问题需要重新彻底研究。病毒介导的信号事件可能有助于在体内各种免疫环境中感染,在这些环境中需要激活细胞状态;换句话说,HIV 可能利用免疫细胞之间共享的趋化因子信号网络来进入下游细胞成分,这些成分可以作为打破细胞屏障的有效工具。这种被病毒劫持的异常信号转导过程可能反过来促进发病机制。在这篇综述中,我们总结了过去和现在关于 HIV 核心受体信号的研究。我们还讨论了核心受体信号在促进病毒感染和发病机制中的可能作用。