Abstract
During long-term tissue culture of spontaneously transformed clones from BALB/c 3T3 mouse-embryo cells, some clones spontaneously begin to produce high titers of endogenous murine type-C viruses. The antigenic properties of these viruses have been analyzed by indirect immunoelectronmicroscopy and can be classified into two distinguishable populations: (a) BALB/c murine myeloma-associated extracellular viruses that carry a specific envelope antigen, xVEA, different from the typical murine leukemia viral envelope antigens; and (b) previously uncharacterized type-C viruses that have neither xVEA nor the murine leukemia viral envelope antigens. The former produces PC1 antigen and the latter might induce a new cell-surface antigen. Neither of these two populations of BALB/3T3 endogenous type-C viruses was able to infect BALB/c cells but both could infect NIH Swiss cells. A single BALB/3T3 clone, then, can release infectious endogenous type-C viruses with at least two different antigenic properties. We conclude that BALB/c somatic cells contain preexisting genetic information for production of at least closely related but, nevertheless, distinct type-C viruses.
MeSH Terms
Animals
Antibodies, Viral
Antigens, Viral
Cell Membrane/immunology
Cell Transformation, Neoplastic
Clone Cells
Embryo, Mammalian
Ferritins
Fibroblasts
Gammaretrovirus/immunology
Genes
Immune Sera
Mice
Mice, Inbred Strains
Microscopy, Electron
Multiple Myeloma/microbiology
Neoplasms, Experimental/microbiology
Oncogenic Viruses/immunology
RNA Viruses/immunology
Retroviridae/immunology
Chemicals
Antibodies, Viral
Antigens, Viral
Immune Sera
Ferritins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Aoki T
Todaro G J
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