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HCMV vCXCL1 Binds Several Chemokine Receptors and Preferentially Attracts Neutrophils over NK Cells by Interacting with CXCR2

机译:HCMV VcxCl1结合几种趋化因子受体,并优选通过与CXCR2相互作用来吸引NK细胞上的中性粒细胞

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HCMV is a highly sophisticated virus that has developed various mechanisms for immune evasion and viral dissemination throughout the body (partially mediated by neutrophils). NK cells play an important role in elimination of HCMV-infected cells. Both neutrophils and NK cells utilize similar sets of chemokine receptors to traffic, to and from, various organs. However, the mechanisms by which HCMV attracts neutrophils and not NK cells are largely unknown. Here, we show a unique viral protein, vCXCL1, which targets three chemokine receptors: CXCR1 and CXCR2 expressed on neutrophils and CXCR1 and CX3CR1 expressed on NK cells. Although vCXCL1 attracted both cell types, neutrophils migrated faster and more efficiently than NK cells through the binding of CXCR2. Therefore, we propose that HCMV has developed vCXCL1 to orchestrate its rapid systemic dissemination through preferential attraction of neutrophils and uses alternative mechanisms to counteract the later attraction of NK cells.
机译:HCMV是一种高度复杂的病毒,它已经开发了整个身体的免疫逃避和病毒散射的各种机制(部分地由中性粒细胞介导)。 NK细胞在消除HCMV感染的细胞中起重要作用。中性粒细胞和NK细胞都利用类似的趋化因子受体与各种器官交通到交通。然而,HCMV吸引中性粒细胞而不是NK细胞的机制在很大程度上是未知的。在这里,我们显示了一种独特的病毒蛋白,VcxCl1,其靶向三个趋化因子受体:CXCR1和CXCR2在中性粒细胞和CXCR1和CX3CR1上表达的CXCR1和CX3CR1。虽然VcxCl1吸引了两种细胞类型,但中性粒细胞通过CXCR2的结合更快地迁移,比NK细胞更快,更有效地迁移。因此,我们提出了HCMV已经开发了VCXCL1,通过中性粒细胞的优先吸引力来协调其快速的全身传播,并使用替代机制来抵消较高的NK细胞的吸引力。

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