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HIV virions sense plasma membrane heterogeneity for cell entry

机译:HIV病毒粒子感知质膜异质性进入细胞

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It has been proposed that cholesterol in host cell membranes plays a pivotal role for cell entry of HIV. However, it remains largely unknown why virions prefer cholesterol-rich heterogeneous membranes to uniformly fluid membranes for membrane fusion. Using giant plasma membrane vesicles containing cholesterol-rich ordered and cholesterol-poor fluid lipid domains, we demonstrate that the HIV receptor CD4 is substantially sequestered into ordered domains, whereas the co-receptor CCR5 localizes preferentially at ordered/disordered domain boundaries. We also show that HIV does not fuse from within ordered regions of the plasma membrane but rather at their boundaries. Ordered/disordered lipid domain coexistence is not required for HIV attachment but is a prerequisite for successful fusion. We propose that HIV virions sense and exploit membrane discontinuities to gain entry into cells. This study provides surprising answers to the long-standing question about the roles of cholesterol and ordered lipid domains in cell entry of HIV and perhaps other enveloped viruses.
机译:已经提出,宿主细胞膜中的胆固醇对于HIV进入细胞起着关键作用。然而,在很大程度上仍然未知,为什么病毒粒子更喜欢富含胆固醇的异质膜而不是均匀的流体膜来进行膜融合。使用包含富含胆固醇的有序和少胆固醇的液体脂质结构域的巨大质膜囊泡,我们证明,HIV受体CD4基本上被隔离到有序域中,而共受体CCR5则优先定位于有序/无序域边界。我们还表明,HIV不会从质膜的有序区域内融合,而是在其边界融合。 HIV附着并不需要有序/无序的脂质域共存,但这是成功融合的前提。我们建议HIV病毒粒子感知并利用膜间断来进入细胞。这项研究为长期存在的有关胆固醇和有序脂质结构域在HIV和其他包膜病毒进入细胞中的作用的问题提供了令人惊讶的答案。

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