Isolation and characterization of an isoantigenic variant from a heterozygous mouse lymphoma in culture.

Abstract

AbstractA cell line from a mouse lymphoma heterozygous at the chromosome region for the H‐2d and H‐2k alleles was originally obtained from a transplantable lymphoma in the (C3H × DBA/2)F1 hybrid (H‐2d/H‐2k) and cultured in vitro. The original cultured line, termed parent line, was susceptible to the cytotoxic action of antibodies directed against antigenic components of both the d and k alleles. The parent line also absorbed hemagglutinins from both anti‐d anti‐k antisera. A resistant, variant subline was selected from the original population by immunoselection in vitro with anti‐H‐2d antibody and complement in a cytotoxic system. After one year in continuous culture in the absence of selecting antisera, the variant subline was still resistant to the cytotoxic action of anti‐H‐2d antibody. Serologic analysis of the variant indicated that it had lost the D antigenic component of the d allele, had a reduced amount of the H component, controlled by both the d and k alleles, and had retained the K component of the k allele. Possible genetic mechanisms that might account for the emergence of the variant line are discussed. While the results do not necessarily support an analysis based on mitotic recombination, ascribing other mechanisms is also difficult because of aneuploidy in the cell line. Finally, the experiments point out the advantages of using in vitro immunoselective methods in the genetics of mammalian somatic cells.