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人免疫缺陷病毒1型体外感染H9细胞和血液单核细胞后宿主细胞膜蛋白。免疫电镜研究。

Host cell membrane proteins on human immunodeficiency virus type 1 after in vitro infection of H9 cells and blood mononuclear cells. An immuno-electron microscopic study.

作者信息

Meerloo T, Sheikh M A, Bloem A C, de Ronde A, Schutten M, van Els C A, Roholl P J, Joling P, Goudsmit J, Schuurman H J

机构信息

Department of Pathology, University Hospital, Utrecht, The Netherlands.

出版信息

J Gen Virol. 1993 Jan;74 ( Pt 1):129-35. doi: 10.1099/0022-1317-74-1-129.

Abstract

Human immunodeficiency virus type 1 (HIV-1)-infected H9 and blood mononuclear cells (MNCs) were studied by immunogold electron microscopy for the presence of HIV-1 gag p24 protein, env gp41 and gp120 proteins, and host cell molecules CD4, CD11a, CD25, CD54, CD63, HLA class I and HLA-DR. Uninfected H9 cells and MNC membranes labelled for CD4, HLA class I and class II, and, at low density, CD11a and CD54; lysosomal structures in the cytoplasm labelled for CD63. The infected cell surface showed immunolabelling for HIV-1 proteins, as did budding particle-like structures. Immunogold labelling of the cell membrane for CD4 was almost non-existent. The level of immunolabelling for CD11a and CD54 on infected cells was greater than that on uninfected cells; this is presumably related to a state of activation during virus synthesis. Budding particle-like structures and free virions in the intercellular space were immunogold-labelled for all host cell markers investigated. This was confirmed by double immunogold labelling using combinations of HIV-1 gag p24 labelling and labelling for the respective host cell molecule. We conclude that virions generated in HIV-1-infected cells concentrate host-derived molecules on their envelope. Also molecules with a prime function in cellular adhesion concentrate on the virion.

摘要

利用免疫金电子显微镜技术,对感染1型人类免疫缺陷病毒(HIV-1)的H9细胞和血液单核细胞(MNC)进行研究,以检测HIV-1 gag p24蛋白、env gp41和gp120蛋白以及宿主细胞分子CD4、CD11a、CD25、CD54、CD63、I类人白细胞抗原(HLA)和II类人白细胞抗原(HLA-DR)的存在情况。未感染的H9细胞和MNC膜标记有CD4、I类和II类HLA,以及低密度的CD11a和CD54;细胞质中的溶酶体结构标记有CD63。被感染的细胞表面显示出HIV-1蛋白的免疫标记,出芽的颗粒样结构也是如此。细胞膜上CD4的免疫金标记几乎不存在。被感染细胞上CD11a和CD54的免疫标记水平高于未感染细胞;这可能与病毒合成过程中的激活状态有关。细胞间空间中的出芽颗粒样结构和游离病毒粒子对所有研究的宿主细胞标记物均进行了免疫金标记。使用HIV-1 gag p24标记与相应宿主细胞分子标记的组合进行双重免疫金标记,证实了这一点。我们得出结论,在HIV-1感染细胞中产生的病毒粒子会在其包膜上浓缩宿主来源的分子。此外,在细胞黏附中起主要作用的分子也会集中在病毒粒子上。

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