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Attenuation of chemokine receptor function and surface expression as an immunomodulatory strategy employed by human cytomegalovirus is linked to vGPCR US28

机译:趋化因子受体功能和表面表达的减弱作为人类巨细胞病毒所采用的免疫调节策略与vGPCR US28相关

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摘要

BackgroundSome herpesviruses like human cytomegalovirus (HCMV) encode viral G protein-coupled receptors that cause reprogramming of cell signaling to facilitate dissemination of the virus, prevent immune surveillance and establish life-long latency. Human GPCRs are known to function in complex signaling networks involving direct physical interactions as well as indirect crosstalk of orthogonal signaling networks. The human chemokine receptor CXCR4 is expressed on hematopoietic stem cells, leukocytes, endothelial and epithelial cells, which are infected by HCMV or display reservoirs of latency.
机译:背景技术一些疱疹病毒(例如人巨细胞病毒(HCMV))编码病毒G蛋白偶联的受体,这些受体引起细胞信号的重新编程,以促进病毒的传播,防止免疫监视并建立终生潜伏期。已知人类GPCR在复杂的信号网络中起作用,该网络涉及直接的物理相互作用以及正交信号网络的间接串扰。人趋化因子受体CXCR4在造血干细胞,白细胞,内皮和上皮细胞上表达,这些细胞被HCMV感染或表现出潜伏期。

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