IMMUNOFLUORESCENCE ANALYSIS OF B-1 CELL ONTOGENY IN THE MOUSE

被引:38
作者
HAMILTON, AM
LEHUEN, A
KEARNEY, JF
机构
[1] UNIV ALABAMA,DEPT MICROBIOL,DIV DEV & CLIN IMMUNOL,BIRMINGHAM,AL 35294
[2] HOP NECKER ENFANTS MALAD,INSERM,U25,F-75743 PARIS 15,FRANCE
关键词
B220; B-CELLS; B-LYMPHOCYTES; CD5; FC-EPSILON-R; SPLEEN; IL-5; RECEPTOR; IGD; IGM; MAC-1; PERITONEAL;
D O I
10.1093/intimm/6.3.355
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In order to further understand the developmental aspects of B-1 cells, we characterized the ontogeny of this B cell population in the spleen and peritoneal cavity of BALB/c mice. Although there are B-1 cells in the spleen within the first 1 - 3 weeks after birth, they do not at any stage represent the majority of splenic B cells. Splenic B-1 cells reach peak levels at approximately 9 days after birth. The mesenteric lining that covers the small intestine of 7-day-old mice contains a population of IgM+ B cells, while at the same age, there are few lymphoid cells in the peritoneal cavity. Between 7 and 8 days after birth there is an influx of B cells into the peritoneal cavity. At 8 days, the first detectable peritoneal B cells appear to be of the B-1 type based on expression of IL-5 receptor and CD5. However, these peritoneal B-1 cells do not express Mac-1. This antigen is not expressed by the majority of peritoneal B-1 cells until 3 weeks. This study indicates that the majority of early splenic B cells are not B-1 cells and it suggests that the mesenteric tissues surrounding the gut contain B lymphocytes which traffic into the peritoneal cavity where they then reside.
引用
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页码:355 / 361
页数:7
相关论文
共 28 条
[1]   RELATIVE CONTRIBUTION OF THE LEUKOCYTE MOLECULES MO1, LFA-1, AND P150,95 (LEUM5) IN ADHESION OF GRANULOCYTES AND MONOCYTES TO VASCULAR ENDOTHELIUM IS TISSUE-SPECIFIC AND STIMULUS-SPECIFIC [J].
ARNAOUT, MA ;
LANIER, LL ;
FALLER, DV .
JOURNAL OF CELLULAR PHYSIOLOGY, 1988, 137 (02) :305-309
[2]   THE ONTOGENY AND FUNCTIONAL-CHARACTERISTICS OF HUMAN B-1 (CD5+B) CELLS [J].
BHAT, NM ;
KANTOR, AB ;
BIEBER, MM ;
STALL, AM ;
HERZENBERG, LA ;
TENG, NNH .
INTERNATIONAL IMMUNOLOGY, 1992, 4 (02) :243-252
[3]  
BOFILL M, 1985, J IMMUNOL, V134, P1531
[4]   TERMINAL DEOXYNUCLEOTIDYL TRANSFERASE-POSITIVE B-CELL PRECURSORS IN FETAL LYMPH-NODES AND EXTRAHEMOPOIETIC TISSUES [J].
CATTORETTI, G ;
PARRAVICINI, C ;
BONATI, A ;
BUSCAGLIA, M ;
ZULIANI, G ;
PLEBANI, A ;
DELIA, D ;
RILKE, F .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1989, 19 (03) :493-500
[5]  
CONG YZ, 1991, INT IMMUNOL, V3, P467
[6]   PREPARATION AND PURIFICATION OF LYMPHOCYTES FROM THE EPITHELIUM AND LAMINA PROPRIA OF MURINE SMALL-INTESTINE [J].
DAVIES, MDJ ;
PARROTT, DMV .
GUT, 1981, 22 (06) :481-488
[7]   A DEVELOPMENTAL SWITCH IN B-LYMPHOPOIESIS [J].
HARDY, RR ;
HAYAKAWA, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (24) :11550-11554
[8]   B-1 CELLS ARE MADE, NOT BORN [J].
HAUGHTON, G ;
ARNOLD, LW ;
WHITMORE, AC ;
CLARKE, SH .
IMMUNOLOGY TODAY, 1993, 14 (02) :84-87
[9]   THE LY-1-B CELL SUBPOPULATION IN NORMAL, IMMUNODEFECTIVE, AND AUTOIMMUNE MICE [J].
HAYAKAWA, K ;
HARDY, RR ;
PARKS, DR ;
HERZENBERG, LA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 157 (01) :202-218
[10]   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