CD19 regulates B lymphocyte responses to transmembrane signals

被引:79
作者
Fujimoto, M [1 ]
Poe, JC [1 ]
Inaoki, M [1 ]
Tedder, TF [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Immunol, Durham, NC 27710 USA
关键词
B lymphocyte; CD19; immunoglobulin; humoral immunity; Src-family protein tyrosine kinase; Vav;
D O I
10.1006/smim.1998.9999
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD19 is a component of a cell surface receptor complex that regulates B lymphocyte responses to transmembrane signals including those generated through the B cell antigen receptor. Studies in mice which lack or overexpress CD19 show that changes in CD19 expression levels have significant effects on B cell development and function. Recent studies suggest that CD19 establishes a Src-family kinase activation loop that amplifies tyrosine phosphorylation of numerous downstream effector molecules including potentially positive and negative regulatory elements. These observations provide an understanding of how CD19 governs the molecular ordering and intensity of signals transduced through multiple B cell receptors.
引用
收藏
页码:267 / 277
页数:11
相关论文
共 82 条
[1]   Disruption of the Cr2 locus results in a reduction in B-1a cells and in an impaired B cell response to T-dependent antigen [J].
Ahearn, JM ;
Fischer, MB ;
Croix, D ;
Goerg, S ;
Ma, MH ;
Xia, JR ;
Zhou, XN ;
Howard, RG ;
Rothstein, TL ;
Carroll, MC .
IMMUNITY, 1996, 4 (03) :251-262
[2]   SIGNALING THROUGH CD19, FC-RECEPTORS OR TRANSFORMING GROWTH-FACTOR-BETA - EACH INHIBITS THE ACTIVATION OF RESTING HUMAN B-CELLS DIFFERENTLY [J].
BARRETT, TB ;
SHU, GL ;
DRAVES, KE ;
PEZZUTTO, A ;
CLARK, EA .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (05) :1053-1059
[3]   The protein product of the proto-oncogene c-cbl forms a complex with phosphatidylinositol 3-kinase p85 and CD19 in anti-IgM-stimulated human B-lymphoma cells [J].
Beckwith, M ;
Jorgensen, G ;
Longo, DL .
BLOOD, 1996, 88 (09) :3502-3507
[4]   A SELECTIVE DEFECT IN IGM ANTIGEN RECEPTOR SYNTHESIS AND TRANSPORT CAUSES LOSS OF CELL-SURFACE IGM EXPRESSION ON TOLERANT B-LYMPHOCYTES [J].
BELL, SE ;
GOODNOW, CC .
EMBO JOURNAL, 1994, 13 (04) :816-826
[5]   IMMUNOGLOBULIN RECOMBINASE GENE ACTIVITY IS MODULATED RECIPROCALLY BY INTERLEUKIN-7 AND CD19 IN B-CELL PROGENITORS [J].
BILLIPS, LG ;
NUNEZ, CA ;
BERTRAND, FE ;
STANKOVIC, AK ;
GARTLAND, GL ;
BURROWS, PD ;
COOPER, MD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (04) :973-982
[6]  
BRADBURY LE, 1992, J IMMUNOL, V149, P2841
[7]  
BRADBURY LE, 1993, J IMMUNOL, V151, P2915
[8]   Qualitative regulation of B cell antigen receptor signaling by CD19: Selective requirement for PI3-kinase activation, inositol-1,4,5-trisphosphate production and Ca2+ mobilization [J].
Buhl, AM ;
Pleiman, CM ;
Rickert, RC ;
Cambier, JC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (11) :1897-1910
[9]   ANTIIMMUNOGLOBULIN STIMULATION OF LYMPHOCYTES-B ACTIVATES SRC-RELATED PROTEIN-TYROSINE KINASES [J].
BURKHARDT, AL ;
BRUNSWICK, M ;
BOLEN, JB ;
MOND, JJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :7410-7414
[10]  
CALLARD RE, 1992, J IMMUNOL, V148, P2983