ONTOGENY OF THYMIC B-CELLS IN NORMAL MICE

被引:36
作者
NANGO, K
INABA, M
INABA, K
ADACHI, Y
THAN, S
ISHIDA, T
KUMAMOTO, T
UYAMA, M
IKEHARA, S
机构
[1] KANSAI MED UNIV,DEPT PATHOL 1,MORIGUCHI,OSAKA 570,JAPAN
[2] KANSAI MED UNIV,DEPT OPHTHALMOL,MORIGUCHI,OSAKA 570,JAPAN
[3] KANSAI MED UNIV,DEPT IMMUNOL,MORIGUCHI,OSAKA 570,JAPAN
[4] KANSAI MED UNIV,LIVER RES CTR,MORIGUCHI,OSAKA 570,JAPAN
[5] KANSAI MED UNIV,DEPT ORTHOPED SURG,MORIGUCHI,OSAKA 570,JAPAN
[6] KYOTO UNIV,FAC SCI,DEPT ZOOL,SAKYO KU,KYOTO 606,JAPAN
关键词
D O I
10.1016/0008-8749(91)90183-C
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ontogeny of thymic B cells and their surface characteristics were analyzed using monoclonal antibodies (mAbs) against B220 molecules (CD45, CD45R). A small number of B cells were detected in fetal thymus on Gestation Day 14 (approximately 3.5% of the low-density fraction). Similarly, the percentage of B cells in the low-density fraction was 3.2% on Gestation Day 18, and 3.5% on Day 1 after birth. These were the same level as that of adult mice. CD5+ B cells, which form the major population of thymic B cells, were also found in the fetal life (0.5% on Day 14 and 2.2% on Day 16 in the low-density cells). The percentage of CD5+ B cells in B cell-enriched fraction was about 65% on Day 1 after birth, which is the same level as that in adult mice. These results indicate that a small number of B cells or cells in the B-cell lineage are present in the fetal thymus and also suggest the importance of these thymic B cells in the negative selection of T cells during early developmental stages. © 1991.
引用
收藏
页码:109 / 115
页数:7
相关论文
共 27 条
  • [1] MIGRATION OF PERIPHERAL T-CELLS AND B-CELLS INTO THE THYMUS OF AGING (NZBXSJL)F1 FEMALE MICE
    DUMONT, FJ
    BARROIS, R
    JACOBSON, EB
    [J]. CELLULAR IMMUNOLOGY, 1984, 83 (02) : 292 - 301
  • [2] SUBSETS OF LYMPHOID-CELLS IN BLOOD AND THYMUS IN MYASTHENIA-GRAVIS - MONOCLONAL-ANTIBODY ANALYSIS
    FUJII, N
    ITOYAMA, Y
    TABIRA, T
    KUROIWA, Y
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1983, 4 (03) : 151 - 159
  • [3] IMMUNOGLOBULIN GENE-EXPRESSION IS A NORMAL DIFFERENTIATION EVENT IN EMBRYONIC THYMOCYTES
    GALLAGHER, PF
    MILLER, JFAP
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (01) : 183 - 186
  • [4] GJEDDE SB, 1980, EXP HEMATOL, V8, P375
  • [5] PERITONEAL LY-1 B-CELLS - GENETIC-CONTROL, AUTOANTIBODY PRODUCTION, INCREASED LAMBDA LIGHT CHAIN EXPRESSION
    HAYAKAWA, K
    HARDY, RR
    HERZENBERG, LA
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1986, 16 (04) : 450 - 456
  • [6] LY-1 B-CELLS - FUNCTIONALLY DISTINCT LYMPHOCYTES THAT SECRETE IGM AUTOANTIBODIES
    HAYAKAWA, K
    HARDY, RR
    HONDA, M
    HERZENBERG, LA
    STEINBERG, AD
    HERZENBERG, LA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (08): : 2494 - 2498
  • [7] IKEHARA S, 1985, THYMUS, V7, P25
  • [8] FUNCTIONAL ANALYSES OF THYMIC CD5+ B-CELLS - RESPONSIVENESS TO MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II-RESTRICTED T-BLASTS BUT NOT TO LIPOPOLYSACCHARIDE OR ANTI-IGM PLUS INTERLEUKIN-4
    INABA, M
    INABA, K
    ADACHI, Y
    NANGO, K
    OGATA, H
    MURAMATSU, S
    IKEHARA, S
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (01) : 321 - 326
  • [9] ISAACSON PG, 1987, LANCET, V2, P1488
  • [10] T-CELL TOLERANCE BY CLONAL ELIMINATION IN THE THYMUS
    KAPPLER, JW
    ROEHM, N
    MARRACK, P
    [J]. CELL, 1987, 49 (02) : 273 - 280