TY - JOUR
T1 - Antibodies specific for Ig idiotype, but not isotype, can substitute for antigen to induce IgM secretion by a B cell clone
AU - Bishop, Gail Abendroth
AU - Pennell, Christopher A.
AU - Travis, William
AU - Haughton, Geoffrey
AU - Frelinger, Jeffrey A.
N1 - Funding Information:
We thank Ms Kathie Lindley for excellent technical assistance in the preparation of the mAbs specific for the CH12 idiotype. This study was supported by grants CA23770 (J A F ) and 420771 (G.H ) from the NIH and IN-122K (G A B.) from the American Cancer Society, administered through the University of Iowa Cancer Center. G.A.B. is an Investigator of the National Arthritis Foundation.
PY - 1990/4
Y1 - 1990/4
N2 - Cells of the mouse B cell clone, CH12.LX, secrete IgM when cultured with nominal antigen (sheep erythrocytes, SRBC) and mAbs which bind their membrane Ek molecules. To determine whether anti-lg antibodies can substitute for antigen In the Induction of IgM secretion by CH12.LX, the B cells were cultured with antl-Ek mAbs and antl-IgM or antl-idiotype antibodies. Anti-IgM antibodies were capable of cross-linking the membrane IgM of CH12.LX, and Inhibited mitogen-induced differentiation of the B cells. However, anti-IgM could not substitute for SRBC In delivering a major histocompatibility complex-restricted differentlative signal. In contrast, either polyclonal or monoclonal antibodies specific for the CH12.LX Ig idlotype were fully capable of substituting for antigen in the induction of IgM secretion by CH12.LX. The binding of anti-IgM antibodies did not prevent anti-Idiotype antibodies from delivering a differentiative signal. Thus, binding of ligand to different parts of the membrane Ig molecule can result in the delivery of different biological signals to the B cell.
AB - Cells of the mouse B cell clone, CH12.LX, secrete IgM when cultured with nominal antigen (sheep erythrocytes, SRBC) and mAbs which bind their membrane Ek molecules. To determine whether anti-lg antibodies can substitute for antigen In the Induction of IgM secretion by CH12.LX, the B cells were cultured with antl-Ek mAbs and antl-IgM or antl-idiotype antibodies. Anti-IgM antibodies were capable of cross-linking the membrane IgM of CH12.LX, and Inhibited mitogen-induced differentiation of the B cells. However, anti-IgM could not substitute for SRBC In delivering a major histocompatibility complex-restricted differentlative signal. In contrast, either polyclonal or monoclonal antibodies specific for the CH12.LX Ig idlotype were fully capable of substituting for antigen in the induction of IgM secretion by CH12.LX. The binding of anti-IgM antibodies did not prevent anti-Idiotype antibodies from delivering a differentiative signal. Thus, binding of ligand to different parts of the membrane Ig molecule can result in the delivery of different biological signals to the B cell.
KW - B cell clone
KW - Differentiation
KW - IgM secretion
KW - Signaling
UR - http://www.scopus.com/inward/record.url?scp=0025273803&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0025273803&partnerID=8YFLogxK
U2 - 10.1093/intimm/2.4.285
DO - 10.1093/intimm/2.4.285
M3 - Article
C2 - 2278988
AN - SCOPUS:0025273803
VL - 2
SP - 285
EP - 290
JO - International Immunology
JF - International Immunology
SN - 0953-8178
IS - 4
ER -