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Transferrin receptor induction is required for human B‐lymphocyte activation but not for immunoglobulin secretion
Author(s) -
Neckers L. M.,
Yenokida G.,
Trepel J. B.,
Lipford E.,
James S.
Publication year - 1985
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.240270407
Subject(s) - transferrin receptor , transferrin , receptor , biology , b cell receptor , antibody , b cell , microbiology and biotechnology , receptor expression , secretion , endocrinology , immunology , biochemistry
Transferrin receptors are expressed on proliferating cells and are required for their growth. Transferrin receptors can be detected after, but not before, mitogenic stimulation of normal peripheral blood T and B cells. In the experiments reported here we have examined the regulation of transferrin receptor expression on activated human B cells and whether or not these receptors are necessary for activation to occur. Activation was assessed by studying both proliferation and immunoglobulin secretion. We have determined that transferrin receptor expression on B cells is regulated by a factor contained in supernatants of mitogenstimulated T cells (probably B‐cell growth factor). This expression is required for proliferation to occur, since antibody to transferrin receptor (42/6) blocks B‐cell proliferation. Induction of immunoglobulin secretion, however, although dependent on PHA‐treated T‐cell supernatant, is not dependent on transferrin receptor expression and can occur in mitogen‐stimulated cells whose proliferation has been blocked by antitransferrin receptor antibody. In addition, we have demonstrated that IgM messenger RNA induction following mitogen stimulation is unaffected by antitransferrin receptor antibody. These findings support a model for B‐cell activation in which mitogen (or antigen) delivers two concurrent but distinct signals to B cells: one, dependent on B‐cell growth factor and transferrin receptor expression, for proliferation, and a second, dependent on T cell‐derived factors and not requiring transferrin receptors, which leads to immunoglobulin secretion.