LYMPHOMA MODELS FOR B-CELL ACTIVATION AND TOLERANCE .8. CROSS-DESENSITIZATION BY SIGM AND SIGD AND ITS EFFECTS ON GROWTH-REGULATION BY ANTIISOTYPE ANTIBODIES

被引:10
作者
ALESMARTINEZ, JE [1 ]
WARNER, GL [1 ]
SCOTT, DW [1 ]
机构
[1] UNIV ROCHESTER,SCH MED & DENT,CTR CANC,IMMUNOL UNIT,BOX 704,601 ELMWOOD AVE,ROCHESTER,NY 14642
关键词
D O I
10.1016/0008-8749(90)90153-I
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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. © 1990.
引用
收藏
页码:527 / 534
页数:8
相关论文
共 11 条
[1]   IMMUNOGLOBULIN-D AND IMMUNOGLOBULIN-M MEDIATE SIGNALS THAT ARE QUALITATIVELY DIFFERENT IN B-CELLS WITH AN IMMATURE PHENOTYPE [J].
ALESMARTINEZ, JE ;
WARNER, GL ;
SCOTT, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (18) :6919-6923
[2]   CROSS-LINKING OF SURFACE-IMMUNOGLOBULIN ON LYMPHOCYTES-B INDUCES BOTH INTRACELLULAR CA-2+ RELEASE AND CA-2+ INFLUX - ANALYSIS WITH INDO-1 [J].
BIJSTERBOSCH, MK ;
RIGLEY, KP ;
KLAUS, GGB .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 137 (01) :500-506
[3]  
BOYD AW, 1981, J IMMUNOL, V126, P2466
[4]   MOLECULAR MECHANISMS OF TRANSMEMBRANE SIGNALING IN LYMPHOCYTES-B [J].
CAMBIER, JC ;
RANSOM, JT .
ANNUAL REVIEW OF IMMUNOLOGY, 1987, 5 :175-199
[5]  
MIZUGUCHI J, 1986, J IMMUNOL, V137, P2162
[6]  
MIZUGUCHI J, 1987, J IMMUNOL, V139, P1054
[7]   LYMPHOMA MODELS FOR B-CELL ACTIVATION AND TOLERANCE .4. GROWTH-INHIBITION BY ANTI-IG OF CH31 AND CH33 B-LYMPHOMA CELLS [J].
PENNELL, CA ;
SCOTT, DW .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1986, 16 (12) :1577-1581
[8]   ROLE OF T-CELL-DERIVED LYMPHOKINES IN 2 MODELS OF B-CELL TOLERANCE [J].
SCOTT, DW ;
CHACE, JH ;
WARNER, GL ;
OGARRA, A ;
KLAUS, GGB ;
QUILL, H .
IMMUNOLOGICAL REVIEWS, 1987, 99 :153-171
[9]  
SCOTT DW, 1987, J MOL CELL IMMUNOL, V3, P109
[10]   FUNCTIONAL DIFFERENCES BETWEEN IMMUNOGLOBULIN-M AND IMMUNOGLOBULIN-D EXPRESSED ON THE SURFACE OF AN IMMATURE B-CELL LINE [J].
TISCH, R ;
ROIFMAN, CM ;
HOZUMI, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (18) :6914-6918