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G(总)和H-2细胞表面抗原:通过电子显微镜和视觉标记抗体确定其在格罗斯白血病细胞上的定位。

G (Gross) and H-2 cell-surface antigens: location on Gross leukemia cells by electron microscopy with visually labeled antibody.

作者信息

Aoki T, Boyse E A, Old L J, De Harven E, Hämmerling U, Wood H A

出版信息

Proc Natl Acad Sci U S A. 1970 Mar;65(3):569-76. doi: 10.1073/pnas.65.3.569.

Abstract

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.

摘要

采用以铁蛋白或南方菜豆花叶病毒作为可视标记,在电子显微镜照片中定位细胞表面抗原的杂交抗体法,对由格罗斯病毒诱导的移植性小鼠白血病细胞进行了研究。所研究的两种抗原为:(a)G(格罗斯)细胞表面抗原,它是感染格罗斯病毒的细胞的一种特异性成分,可被细胞毒性超免疫C57BL/6抗血清识别;(b)H-2抗原,它是小鼠的主要组织相容性决定簇。两种抗原在细胞表面均以离散的限定区域形式呈现。在游离的格罗斯病毒粒子或从细胞表面出芽过程中的病毒粒子上均未发现这两种抗原。因此,由C57BL小鼠细胞毒性抗血清识别的G细胞表面抗原不是病毒包膜的组成成分,这就解释了此类抗体的病毒中和能力较差的原因。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(+)区域很少见到出芽现象,而在G(+)区域从未有令人信服的出芽现象。在其他实验中,16月龄未处理的NZB小鼠的血清仅使病毒粒子产生标记,这表明与C57BL和其他品系相比,该小鼠品系可形成针对格罗斯病毒包膜抗原的抗体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a02/282945/25d5f8d6c108/pnas00094-0097-a.jpg

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