首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >G (Gross) and H-2 Cell-Surface Antigens: Location on Gross Leukemia Cells by Electron Microscopy with Visually Labeled Antibody
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G (Gross) and H-2 Cell-Surface Antigens: Location on Gross Leukemia Cells by Electron Microscopy with Visually Labeled Antibody

机译:G(总)和H-2细胞表面抗原:电子显微镜下视觉标记的抗体在总白血病细胞上的位置。

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摘要

The hybrid-antibody method of locating cell-surface antigens in electron micrographs, with either ferritin or southern bean mosaic virus as the visual marker, was applied to the cells of a transplanted murine leukemia induced by Gross virus. The two antigens studied were (a) G (Gross) cell-surface antigen, which is a specific component of cells infected with Gross virus and is identified by cytotoxic hyperimmune C57BL/6 antiserum, and (b) H-2 antigen, which is the major histocompatibility determinant of the mouse.Both antigens were represented on the cell surface in discrete circumscribed areas. Neither antigen was present on free Gross virions or on virions in the process of budding from the cell surface.Thus G cell-surface antigen identified by C57BL mouse cytotoxic antiserum is not a constituent of the viral envelope, which accounts for the poor virus-neutralizing capacity of such antibody.Virus maturation may take place preferentially at regions of the cell surface where H-2 and G antigens are absent, for budding was seldom seen in H-2+ sectors and never convincingly in G+ sectors.In other experiments, serum from an untreated NZB mice aged 16 months gave labeling of the virion only, showing that this mouse strain, in contrast to C57BL and other strains, forms antibody to envelope antigen of Gross virus.
机译:以铁蛋白或南方豆花叶病毒为视觉标记,在电子显微照片中定位细胞表面抗原的杂交抗体方法被应用于由格罗斯病毒诱导的移植鼠白血病的细胞。研究的两种抗原是(a)G(Gross)细胞表面抗原,是被格罗斯病毒感染的细胞的特定成分,并通过细胞毒性超免疫C57BL / 6抗血清鉴定;以及(b)H-2抗原,其是这是小鼠的主要组织相容性决定因素。两种抗原均在离散的外接区域的细胞表面上表达。游离毛状病毒粒子或病毒粒子从细胞表面出芽的过程中都没有抗原。因此,C57BL小鼠细胞毒性抗血清鉴定出的G细胞表面抗原不是病毒被膜的成分,这说明病毒中和性差病毒成熟可能优先发生在细胞表面不存在H-2和G抗原的区域,因为在H-2 + 区域很少见到出芽,而在G却从未令人信服在其他实验中,未经治疗的16个月大的NZB小鼠的血清仅标记了病毒体,表明该小鼠品系与C57BL和其他品系相反,形成了针对C57BL包膜抗原的抗体严重病毒。

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