Pelchen-Matthews A, Signoret N, Klasse P J, Fraile-Ramos A, Marsh M
MRC Laboratory for Molecular Cell Biology, University College London, UK.
Immunol Rev. 1999 Apr;168:33-49. doi: 10.1111/j.1600-065x.1999.tb01281.x.
Chemokines and chemokine receptors have emerged as crucial factors controlling the development and function of leukocytes. Recent studies have indicated that, in addition to these essential roles, both chemokines and chemokine receptors play critical roles in viral infection and replication. Not only are chemokine receptors key components of the receptor/fusion complexes of primate immunodeficiency viruses, but chemokines can also influence virus entry and infection. Many viruses, in particular herpesviruses, encode chemokines and chemokine receptors that influence the replication of both the parent virus and other unrelated viruses. The cell surface expression of the chemokine receptors is regulated through their interaction with membrane trafficking pathways. Ligands induce receptor internalization and downmodulation through endocytosis, and recycling is regulated within endosomes. Part of the mechanism through which chemokines protect cells from HIV infection is through ligand-induced internalization of the specific chemokine receptor co-receptors. In addition, mechanisms may exist to regulate the trafficking of newly synthesized receptors to the cell surface. Here we discuss aspects of the mechanisms through which chemokine receptors interact with membrane-trafficking pathways and the influence of these interactions on viral replication.
趋化因子和趋化因子受体已成为控制白细胞发育和功能的关键因素。最近的研究表明,除了这些基本作用外,趋化因子和趋化因子受体在病毒感染和复制中也起着关键作用。趋化因子受体不仅是灵长类免疫缺陷病毒受体/融合复合物的关键组成部分,而且趋化因子还能影响病毒的进入和感染。许多病毒,特别是疱疹病毒,编码趋化因子和趋化因子受体,这些因子会影响亲代病毒和其他无关病毒的复制。趋化因子受体的细胞表面表达通过它们与膜运输途径的相互作用来调节。配体通过内吞作用诱导受体内化和下调,并且在内体中调节再循环。趋化因子保护细胞免受HIV感染的部分机制是通过配体诱导特定趋化因子受体共受体的内化。此外,可能存在调节新合成受体向细胞表面运输的机制。在这里,我们讨论趋化因子受体与膜运输途径相互作用的机制方面,以及这些相互作用对病毒复制的影响。