EXTENSIVE SPLENIC B-CELL ACTIVATION IN IGM-TRANSGENIC MICE

被引:28
作者
FORNI, L
机构
[1] Basel Institute for Immunology, Basel
关键词
D O I
10.1002/eji.1830200506
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Two lines of IgMtransgenic mice were analyzed for the state of activation of their splenic compartment, with regard to the frequency of large cells in the different lymphoid subpopulations, and to the isotype distribution of background plasma cells. We observed an extensive B cell activation preferentially involving B lymphocytes co‐expressing transgenic and endogenous IgM (IgD), and resulting in massive immunoglobulin classswitch. Nearly all splenic plasma cells contain endogenous immunoglobulins, withfrequencies of IgG and IgA plasma cells significantly higher than in normal mice. There are virtually no plasma cells that produce only the transgenic IgM. Moreover, only a proportion ofplasma cells producing endogenous immunoglobulins co‐express the transgenic product. In addition to these observations that apply to both transgenic lines, differences were found between the two lines concerning the quantitative expression of the transgenic IgM, the frequency of cells expressing the transgene and the magnitude of switch. These data are indicative of the complexity of the IgMtransgenic mouse model, in which the phenomenology may depend on the transgene insertional position, on B cell physiology and on immunological mechanisms of recognition, induction and regulation. Copyright © 1990 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
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页码:983 / 989
页数:7
相关论文
共 35 条
[1]   ISOTYPE SWITCHING BY A MICROINJECTED MU-IMMUNOGLOBULIN HEAVY-CHAIN GENE IN TRANSGENIC MICE [J].
DURDIK, J ;
GERSTEIN, RM ;
RATH, S ;
ROBBINS, PF ;
NISONOFF, A ;
SELSING, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (07) :2346-2350
[2]  
Fagraeus A., 1948, ACTA MED SCAND S
[3]  
FORNI L, 1984, METHOD ENZYMOL, V108, P413
[4]   IGM ANTIBODIES INDUCE THE PRODUCTION OF ANTIBODIES OF THE SAME SPECIFICITY [J].
FORNI, L ;
COUTINHO, A ;
KOHLER, G ;
JERNE, NK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (02) :1125-1128
[5]   ALTERED IMMUNOGLOBULIN EXPRESSION AND FUNCTIONAL SILENCING OF SELF-REACTIVE LYMPHOCYTES-B IN TRANSGENIC MICE [J].
GOODNOW, CC ;
CROSBIE, J ;
ADELSTEIN, S ;
LAVOIE, TB ;
SMITHGILL, SJ ;
BRINK, RA ;
PRITCHARDBRISCOE, H ;
WOTHERSPOON, JS ;
LOBLAY, RH ;
RAPHAEL, K ;
TRENT, RJ ;
BASTEN, A .
NATURE, 1988, 334 (6184) :676-682
[6]   INTRODUCTION OF A MU-IMMUNOGLOBULIN GENE INTO THE MOUSE GERM LINE - SPECIFIC EXPRESSION IN LYMPHOID-CELLS AND SYNTHESIS OF FUNCTIONAL ANTIBODY [J].
GROSSCHEDL, R ;
WEAVER, D ;
BALTIMORE, D ;
COSTANTINI, F .
CELL, 1984, 38 (03) :647-658
[7]   USE OF AVIDIN-BIOTIN COMPLEX FOR SPECIFIC STAINING OF BIOLOGICAL-MEMBRANES IN ELECTRON-MICROSCOPY [J].
HEITZMAN.H ;
RICHARDS, FM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (09) :3537-3541
[8]   DEPLETION OF THE PREDOMINANT B-CELL POPULATION IN IMMUNOGLOBULIN-MU HEAVY-CHAIN TRANSGENIC MICE [J].
HERZENBERG, LA ;
STALL, AM ;
BRAUN, J ;
WEAVER, D ;
BALTIMORE, D ;
HERZENBERG, LA ;
GROSSCHEDL, R .
NATURE, 1987, 329 (6134) :71-73
[9]   IDIOTYPIC CHARACTERIZATION OF ANTIBODY-INDUCED ANTIBODY-RESPONSES [J].
HOLMBERG, D ;
IVARS, F ;
FORNI, L ;
CAZENAVE, PA ;
COUTINHO, A .
IMMUNOBIOLOGY, 1982, 162 (01) :56-65
[10]   EXPRESSION OF IMMUNOGLOBULIN DELTA CHAIN CAUSES ALLELIC EXCLUSION IN TRANSGENIC MICE [J].
IGLESIAS, A ;
LAMERS, M ;
KOHLER, G .
NATURE, 1987, 330 (6147) :482-484