Arrest of B lymphocyte terminal differentiation by CD40 signaling: Mechanism for lack of antibody-secreting cells in germinal centers

被引:119
作者
Randall, TD
Heath, AW
Santos-Argumedo, L
Howard, MC
Weissman, IL
Lund, FE
机构
[1] Trudeau Inst Inc, Saranac Lake, NY 12983 USA
[2] Univ Sheffield, Sch Med, Dept Med Microbiol, Sheffield S10 2RX, S Yorkshire, England
[3] Univ Sheffield, Sch Med, Sheffield Inst Vaccine Studies, Sheffield S10 2RX, S Yorkshire, England
[4] CINVESTAV,IPN, Dept Cell Biol, Mexico City, DF, Mexico
[5] Anergen, Redwood City, CA 94063 USA
[6] Stanford Univ, Dept Pathol, Stanford, CA 94305 USA
关键词
D O I
10.1016/S1074-7613(00)80578-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite extensive research, the role of CD40 signaling in B cell terminal differentiation remains controversial. Here we show that CD40 engagement arrests B cell differentiation prior to plasma cell formation. This arrest is manifested at a molecular level as a reduction in mRNA levels of secretory immunoglobulin gene products such as mu(s) and J chain as well as the loss of the transcriptional regulator BLIMP-1. Furthermore, the inhibition of B cell differentiation by CD40 engagement could not be overcome by either mitogens or cytokines, but could be reversed by antibodies that interfere with the CD40/gp39 interaction. These data suggest that secretory immunoglobulin is not produced by B cells that are actively engaged by gp39-expressing T cells.
引用
收藏
页码:733 / 742
页数:10
相关论文
共 47 条
[1]  
ARMITAGE RJ, 1993, J IMMUNOL, V150, P3671
[2]   MOLECULAR AND BIOLOGICAL CHARACTERIZATION OF A MURINE LIGAND FOR CD40 [J].
ARMITAGE, RJ ;
FANSLOW, WC ;
STROCKBINE, L ;
SATO, TA ;
CLIFFORD, KN ;
MACDUFF, BM ;
ANDERSON, DM ;
GIMPEL, SD ;
DAVISSMITH, T ;
MALISZEWSKI, CR ;
CLARK, EA ;
SMITH, CA ;
GRABSTEIN, KH ;
COSMAN, D ;
SPRIGGS, MK .
NATURE, 1992, 357 (6373) :80-82
[3]   Memory B cells are biased towards terminal differentiation: A strategy that may prevent repertoire freezing [J].
Arpin, C ;
Banchereau, J ;
Liu, YJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (06) :931-940
[4]   GENERATION OF MEMORY B-CELLS AND PLASMA-CELLS IN-VITRO [J].
ARPIN, C ;
DECHANET, J ;
VANKOOTEN, C ;
MERVILLE, P ;
GROUARD, G ;
BRIERE, F ;
BANCHEREAU, J ;
LIU, YJ .
SCIENCE, 1995, 268 (5211) :720-722
[5]   THE CD40 LIGAND, GP39, IS DEFECTIVE IN ACTIVATED T-CELLS FROM PATIENTS WITH X-LINKED HYPER-IGM SYNDROME [J].
ARUFFO, A ;
FARRINGTON, M ;
HOLLENBAUGH, D ;
LI, X ;
MILATOVICH, A ;
NONOYAMA, S ;
BAJORATH, J ;
GROSMAIRE, LS ;
STENKAMP, R ;
NEUBAUER, M ;
ROBERTS, RL ;
NOELLE, RJ ;
LEDBETTER, JA ;
FRANCKE, U ;
OCHS, HD .
CELL, 1993, 72 (02) :291-300
[6]  
AUFFRAY C, 1980, EUR J BIOCHEM, V107, P303
[7]   LONG-TERM HUMAN B-CELL LINES DEPENDENT ON INTERLEUKIN-4 AND ANTIBODY TO CD40 [J].
BANCHEREAU, J ;
DEPAOLI, P ;
VALLE, A ;
GARCIA, E ;
ROUSSET, F .
SCIENCE, 1991, 251 (4989) :70-72
[8]   CRYSTAL-STRUCTURE OF THE SOLUBLE HUMAN 55 KD TNF RECEPTOR-HUMAN TNF-BETA COMPLEX - IMPLICATIONS FOR TNF RECEPTOR ACTIVATION [J].
BANNER, DW ;
DARCY, A ;
JANES, W ;
GENTZ, R ;
SCHOENFELD, HJ ;
BROGER, C ;
LOETSCHER, H ;
LESSLAUER, W .
CELL, 1993, 73 (03) :431-445
[9]  
BJORCK P, 1993, IMMUNOLOGY, V78, P218
[10]  
CALLAGHAN R, 1995, WESTERLY, V40, P11