TY - JOUR
T1 - Lymphoma models for B cell activation and tolerance. VIII. Cross-desensitization by slgM and slgD and its effects on growth regulation by anti-isotype antibodies
AU - Alés-Martínez, JoséE E.
AU - Warner, Garvin L.
AU - Scott, David W.
N1 - Funding Information:
’ This is Publication No. 58 of the Immunology Unit of the Cancer Center. This work was supported by ACS Grant IM-495, a Wilmot Foundation Fellowship (J.A.M.), and USPHS Training Grant AI-07285. ’ To whom all correspondence should be sent at University of Rochester Cancer Center, Box 704, 60 1 Elmwood Avenue, Rochester, NY 14642.
PY - 1990/5
Y1 - 1990/5
N2 - ECH408-1 is a murine B cell lymphoma expressing idiotypically and allotypically distinguishable transfected and endogenous IgD. Previously, we demonstrated that this cell line was not growth inhibited by antibodies directed at membrane IgD, but could be inhibited by antibodies which crosslink membrane IgM. Herein, we demonstrate that both anti-μ and anti-δ will cause calcium mobilization in this transfected cell line; this is followed by a period during which antibodies against the alternative isotype are unable to induce significant increases in intracellular calcium concentrations. This phenomenon, called "desensitization," is short-lived, lasting 20 min. We further demonstrate that acute desensitization of these cells by anti-δ has no effect on immediate growth inhibition which is elicited by anti-μ. These data confirm our earlier proposal that the rapid, initial calcium response seen in these lymphomas is not required for the negative signal for growth. Moreover, we also demonstrate that pretreatment of these lymphoma cells with phorbol myristate acetate (PMA) also renders these lymphoma cells temporarily incapable of manifesting a significant calcium signal. Nonetheless, PMA-pretreated B lymphoma cells are not altered in their subsequent sensitivity to anti-μ growth inhibition, nor are they affected in their resistance to inhibition by anti-δ. Our data confirm the proposal that neither the calcium signal nor protein kinase-C activation is involved in the modulation of B lymphoma growth.
AB - ECH408-1 is a murine B cell lymphoma expressing idiotypically and allotypically distinguishable transfected and endogenous IgD. Previously, we demonstrated that this cell line was not growth inhibited by antibodies directed at membrane IgD, but could be inhibited by antibodies which crosslink membrane IgM. Herein, we demonstrate that both anti-μ and anti-δ will cause calcium mobilization in this transfected cell line; this is followed by a period during which antibodies against the alternative isotype are unable to induce significant increases in intracellular calcium concentrations. This phenomenon, called "desensitization," is short-lived, lasting 20 min. We further demonstrate that acute desensitization of these cells by anti-δ has no effect on immediate growth inhibition which is elicited by anti-μ. These data confirm our earlier proposal that the rapid, initial calcium response seen in these lymphomas is not required for the negative signal for growth. Moreover, we also demonstrate that pretreatment of these lymphoma cells with phorbol myristate acetate (PMA) also renders these lymphoma cells temporarily incapable of manifesting a significant calcium signal. Nonetheless, PMA-pretreated B lymphoma cells are not altered in their subsequent sensitivity to anti-μ growth inhibition, nor are they affected in their resistance to inhibition by anti-δ. Our data confirm the proposal that neither the calcium signal nor protein kinase-C activation is involved in the modulation of B lymphoma growth.
UR - http://www.scopus.com/inward/record.url?scp=0025236886&partnerID=8YFLogxK
U2 - 10.1016/0008-8749(90)90153-I
DO - 10.1016/0008-8749(90)90153-I
M3 - Article
C2 - 2328538
AN - SCOPUS:0025236886
SN - 0008-8749
VL - 127
SP - 527
EP - 534
JO - Cellular Immunology
JF - Cellular Immunology
IS - 2
ER -