G (Gross) and H-2 Cell-Surface Antigens: Location on Gross Leukemia Cells by Electron Microscopy with Visually Labeled Antibody

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 a...

Full description

Saved in:
Bibliographic Details
Published inProceedings of the National Academy of Sciences - PNAS Vol. 65; no. 3; pp. 569 - 576
Main Authors Aoki, Tadao, Boyse, Edward A., Old, Lloyd J., de Harven, Etienne, Hammerling, Ulrich, Wood, Harry A.
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences of the United States of America 01.03.1970
National Acad Sciences
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary: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.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
This investigation was supported by National Cancer Institute grant CA 08748, a grant from the John A. Hartford Foundation, Inc., and PHS grant 1S01 FRO 5679-01.
Present address: Institut für Virologie der Medizinischen Fakultät der Justus Liebig-Universität Giessen, 6300 Giessen, Germany.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.65.3.569