首页> 美国卫生研究院文献>Journal of Virology >Note: Level of ICAM-1 Surface Expression on Virus Producer Cells Influences both the Amount of Virion-Bound Host ICAM-1 and Human Immunodeficiency Virus Type 1 Infectivity
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Note: Level of ICAM-1 Surface Expression on Virus Producer Cells Influences both the Amount of Virion-Bound Host ICAM-1 and Human Immunodeficiency Virus Type 1 Infectivity

机译:注意:病毒生产细胞上ICAM-1表面表达的水平会影响结合病毒的宿主ICAM-1和人免疫缺陷病毒1型感染性的数量

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摘要

Using virions harvested from 293T cells stably expressing either low or high levels of surface ICAM-1, we determined that the number of virus-embedded host ICAM-1 proteins is positively influenced by the expression level of ICAM-1 on virus producer cells. Moreover, the increase in virion-bound host cell membrane ICAM-1 led to a concomitant enhancement of virus infectivity when a T-cell-tropic strain of human immunodeficiency virus type 1 (HIV-1) was used. The phenomenon was also seen when primary human cells were infected with virions pseudotyped with the envelope protein from a macrophage-tropic HIV-1 isolate, thus ruling out any envelope-specific effect. We also observed that target cells treated with NKI-L16, an anti-LFA-1 antibody known to increase the affinity of LFA-1 for ICAM-1, were markedly more susceptible to infection with HIV-1 particles bearing on their surfaces large numbers of host-derived ICAM-1 proteins. Given that cellular activation of leukocytes is known to modify the conformational state of LFA-1 and induce ICAM-1 surface expression, it is tempting to speculate that activation of virus-infected cells will lead to the production of HIV-1 particles bearing more host ICAM-1 on their surfaces and that such progeny virions will preferentially infect and replicate more efficiently in activated cells which are prevalent in lymphoid organs.
机译:使用从稳定表达低水平或高水平表面ICAM-1的293T细胞收获的病毒体,我们确定病毒包埋的宿主ICAM-1蛋白的数量受到ICAM-1在病毒生产细胞上的表达水平的积极影响。此外,当使用人免疫缺陷病毒1型(HIV-1)的T细胞嗜性株时,结合病毒体的宿主细胞膜ICAM-1的增加导致病毒感染性的同时增强。当原代人类细胞感染了巨噬细胞型HIV-1分离株的包膜蛋白假型化病毒体后,也发现了这种现象,从而排除了任何包膜特异性作用。我们还观察到,用NKI-L16(一种已知可增加LFA-1对ICAM-1的亲和力的抗LFA-1抗体)处理的靶细胞,明显更容易感染携带大量表面的HIV-1颗粒。来自宿主的ICAM-1蛋白。鉴于已知白细胞的细胞活化会改变LFA-1的构象状态并诱导ICAM-1表面表达,因此很容易推测,病毒感染细胞的活化将导致携带更多宿主的HIV-1颗粒的产生。 ICAM-1在其表面上,并且这种子代病毒体将优先感染并在淋巴器官中普遍存在的活化细胞中更有效地复制。

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