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从HIV包膜中排除HIV共受体CXCR4、CCR5和CCR3。

Exclusion of HIV coreceptors CXCR4, CCR5, and CCR3 from the HIV envelope.

作者信息

Lallos L B, Laal S, Hoxie J A, Zolla-Pazner S, Bandres J C

机构信息

Research Center for AIDS and HIV Infection, Manhattan VA Medical Center, New York University Medical School, New York 10010, USA.

出版信息

AIDS Res Hum Retroviruses. 1999 Jul 1;15(10):895-7. doi: 10.1089/088922299310601.

Abstract

Both HIV-1 primary isolates and laboratory strains incorporate cell-derived molecules into their envelopes depending on the host cell in which they are grown. This incorporation is not random and, specifically, HIV-1 has been shown to select against the incorporation into its surface of CD4, its main receptor. In this study, we have looked at the incorporation of HIV coreceptors CXCR4, CCR5, and CCR3 into the HIV envelope. For this purpose, we grew HIV-1 primary isolate BZ167 in several cell lines and PBMCs, and the envelope profiles of the resulting viruses were determined with a virus-binding ELISA. While the virus particle gained several molecules when passed through the different cell lines (e.g., ICAM-3, LFA-1, ICAM-1, or MHC class II), BZ167 never incorporated significant levels of CXCR4, CCR5, or CCR3 into its envelope even though some or all of the cell lines in which it was grown expressed them. These results show that HIV-1 selects against the incorporation of these chemokine receptors into its envelope molecule, as it does against the incorporation of CD4.

摘要

HIV-1原代分离株和实验室毒株都会根据其生长所在的宿主细胞,将细胞衍生分子纳入其包膜。这种纳入并非随机发生,具体而言,已有研究表明HIV-1会避免将其主要受体CD4纳入其表面。在本研究中,我们观察了HIV共受体CXCR4、CCR5和CCR3纳入HIV包膜的情况。为此,我们在几种细胞系和外周血单核细胞(PBMC)中培养HIV-1原代分离株BZ167,并通过病毒结合酶联免疫吸附测定(ELISA)确定所得病毒的包膜概况。虽然病毒颗粒在通过不同细胞系时获得了几种分子(如细胞间黏附分子-3(ICAM-3)、淋巴细胞功能相关抗原-1(LFA-1)、ICAM-1或II类主要组织相容性复合体(MHC)),但即使BZ167生长所在的部分或所有细胞系都表达CXCR4、CCR5或CCR3,BZ167也从未将显著水平的这些共受体纳入其包膜。这些结果表明,HIV-1如同避免将CD4纳入其包膜一样,也会避免将这些趋化因子受体纳入其包膜分子。

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