Abstract
Attempts were made to identify the non-Ig lymphocyte receptor responsible for B-cell induction by antigen and polyclonal B-cell activators (PBA). As a first step, the role of C'3 and Fc receptors was analyzed. It was shown that complement could be fixed onto B cells to such an extent that the lymphocytes could not bind complement-coated red cells, but this did not result in induction of polyclonal antibody synthesis, nor did it inhibit the lymphocytes response to PBA. However, the C'3 receptros possessed a passive focussing role in the induction of polyclonal antibody responses. Thus, PBA that had fixed complement activated polyclonal responses at lower concentrations than the same substances that had not fixed complement. Most likely the dual binding of PBA molecules to B cells by the PBA and the C'3 receptors caused more PBA molecules to be bound to each cell. However, the focussing function of the C'3 receptors was several orders of magnitude smaller than that of the Ig receptors. Analogous studies were carried out with Fc receptors. Binding of different types of antigen-antibody complexes did not cause activation of polyclonal or specific antibody synthesis, nor did it significantly interfere with induction of antibody synthesis by PBA substances.
MeSH Terms
Animals
Antibody Formation
Antigen-Antibody Complex
B-Lymphocytes/drug effects,immunology,metabolism
Binding Sites, Antibody
Cell Membrane/immunology
Complement System Proteins
DNA/biosynthesis
Depression, Chemical
Dextrans/analogs & derivatives,pharmacology
Erythrocytes/immunology
Hemolytic Plaque Technique
Immunoglobulin Fc Fragments
Lipopolysaccharides/pharmacology
Lymphocyte Activation
Mice
Mice, Inbred A
Mice, Inbred CBA
Mice, Inbred Strains
Mitogens/pharmacology
Rabbits/immunology
Sheep/immunology
Spleen/cytology
Stearic Acids/analogs & derivatives,pharmacology
Tuberculin
Chemicals
Antigen-Antibody Complex
Dextrans
Immunoglobulin Fc Fragments
Lipopolysaccharides
Mitogens
Stearic Acids
Tuberculin
Complement System Proteins
DNA
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Möller G
Coutinho A
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