Abstract
The frequency of murine B lymphocytes that respond to antibodies directed against membrane IgM was measured. These anti-mu antibodies induced all, or almost all, resting B cells to enlarge over the first 24 h of stimulation. This probably represents the transition from the resting state (G0) to active transit through the cell cycle. In contrast, only a fraction of these cells, approximately 60% for BDF1 mice, continued through the cell cycle into S phase. This is consistent with previous experiments that had suggested there were some types of B cells that did not proliferate in response to anti-mu. The results presented here demonstrate that many, perhaps all, of these nonresponding B cells, both from normal mice and from mice with the xid defect, actually do respond to the presence of anti-mu by going through early parts of the cell cycle. These cells appear to become blocked at some point before the beginning of S phase, perhaps requiring a signal from a T cell or a macrophage to continue through the cell cycle. Thus, the role of antigen may be to prepare all B cells for proliferation. Different subpopulations of B cells may then require different regulatory signals before actually proliferating or before differentiating into antibody-secreting cells.
MeSH Terms
Animals
Antibodies, Anti-Idiotypic/immunology
B-Lymphocytes/classification
Cell Cycle
Cell Separation
Centrifugation, Density Gradient
Female
Immunoglobulin Heavy Chains/immunology
Immunoglobulin mu-Chains/immunology
Lipopolysaccharides/pharmacology
Lymphocyte Activation
Male
Mice
Mice, Inbred C57BL
Mice, Inbred CBA
Mice, Inbred DBA
Receptors, Antigen, B-Cell
Chemicals
Antibodies, Anti-Idiotypic
Immunoglobulin Heavy Chains
Immunoglobulin mu-Chains
Lipopolysaccharides
Receptors, Antigen, B-Cell
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Defranco A L
Raveche E S
Asofsky R
Paul W E
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22 references, click to expand
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