hiv -碳水化合物相互作用的研究进展:来自CXCR4-Tropic病毒的GP120增强了CCR5-Tropic HIV-1的感染性

Birco Schwalbe, H. Hauser, M. Schreiber
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引用次数: 1

摘要

人类免疫缺陷病毒1型是高度可变的,利用两种独立的途径,一种通过CCR5辅助受体,另一种通过CXCR4进入CD4+细胞。在hiv -1感染患者中可以同时发现这两种病毒类型,向大多数嗜cxcr4病毒的转变是艾滋病相关症状发展的一个指标。据认为,每种病毒类型将通过其特定的辅助受体途径独立地感染细胞。在这篇简短的文章中,我们证明了嗜ccr5的HIV-1被嗜cxcr4病毒的包膜增强。当用溴己二甲基菊酯预处理靶细胞时,这种交叉增强效应被完全抑制,这表明细胞膜上的碳水化合物结构在包膜依赖性增强病毒进入中起重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Progress in HIV-Carbohydrate Interactions: Infectivity of CCR5-Tropic HIV-1 is Enhanced by GP120 from CXCR4-Tropic Virus
Human immunodeficiency virus type-1 is highly variable and utilizes two independent pathways, one via the CCR5 coreceptor and the other via CXCR4 to enter CD4+ cells. Both virus types can simultaneously be found in HIV-1-infected patients and the shift to a majority of CXCR4-tropic viruses is an indication for the development of AIDS-related symptoms. It is thought that each virus type will infect cells independently using its specific coreceptor pathways. In this short communication we demonstrate that CCR5-tropic HIV-1 is enhanced by the envelope from CXCR4-tropic viruses. This cross-enhancing effect was completely suppressed when the target cells were pretreated with hexadimethrine bromide, suggesting that carbohydrate structures on the cellular membrane play an important role for envelope-dependent enhancement of viral entry.
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