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

被引:43
作者
INABA, M
INABA, K
ADACHI, Y
NANGO, K
OGATA, H
MURAMATSU, S
IKEHARA, S
机构
[1] KANSAI MED UNIV,DEPT PATHOL 1,FUMIZONO CHO,MORIGUCHI,OSAKA 570,JAPAN
[2] KANSAI MED UNIV,LIVER RES INST,MORIGUCHI,OSAKA 570,JAPAN
[3] KANSAI MED UNIV,DEPT OPHTHALMOL,MORIGUCHI,OSAKA 570,JAPAN
[4] KYOTO UNIV,FAC SCI,DEPT ZOOL,KYOTO 606,JAPAN
关键词
D O I
10.1084/jem.171.1.321
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The function of thymic B cells in several standard in vitro assays was investigated. Thymic B cells, 75% of which were CD5+, showed a poor responsiveness to the mitogens LPS or anti-μ plus IL-4. Both proliferation and antibody formation were much lower in thymic than splenic B cell cultures. However, CD5- B cells purified using a cell sorter responded well to B cell stimulants, whereas purified CD5+ thymic B cells did not, indicating that CD5+ thymic B cells were unresponsive to B cell growth factor or LPS. Thymic B cells could be activated polyclonally by indirect interaction with alloreactive T blasts, as manifested by DNA synthesis and antibody formation. These findings indicate that CD5+ thymic B cells may not be stimulated via sIg and IL-4, but require instead direct interaction with T blasts.
引用
收藏
页码:321 / 326
页数:6
相关论文
共 10 条
  • [1] HUMAN-LYMPHOCYTES MAKING RHEUMATOID-FACTOR AND ANTIBODY TO SSDNA BELONG TO LEU-1+ B-CELL SUBSET
    CASALI, P
    BURASTERO, SE
    NAKAMURA, M
    INGHIRAMI, G
    NOTKINS, AL
    [J]. SCIENCE, 1987, 236 (4797) : 77 - 81
  • [2] RHEUMATOID-FACTOR SECRETION FROM HUMAN LEU-1+ B-CELLS
    HARDY, RR
    HAYAKAWA, K
    SHIMIZU, M
    YAMASAKI, K
    KISHIMOTO, T
    [J]. SCIENCE, 1987, 236 (4797) : 81 - 83
  • [3] DEVELOPMENT AND PHYSIOLOGY OF LY-1 B AND ITS HUMAN HOMOLOG, LEU-1 B
    HARDY, RR
    HAYAKAWA, K
    [J]. IMMUNOLOGICAL REVIEWS, 1986, 93 : 53 - 79
  • [4] 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
  • [5] THE LY-1-B CELL SUBPOPULATION IN NORMAL, IMMUNODEFECTIVE, AND AUTOIMMUNE MICE
    HAYAKAWA, K
    HARDY, RR
    PARKS, DR
    HERZENBERG, LA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 157 (01) : 202 - 218
  • [6] THE LY-1 B-CELL LINEAGE
    HERZENBERG, LA
    STALL, AM
    LALOR, PA
    SIDMAN, C
    MOORE, WA
    PARKS, DR
    HERZENBERG, LA
    [J]. IMMUNOLOGICAL REVIEWS, 1986, 93 : 81 - 102
  • [7] RESTING AND SENSITIZED LYMPHOCYTES-T EXHIBIT DISTINCT STIMULATORY (ANTIGEN-PRESENTING CELL) REQUIREMENTS FOR GROWTH AND LYMPHOKINE RELEASE
    INABA, K
    STEINMAN, RM
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (06) : 1717 - 1735
  • [8] Isaacson P G, 1987, Lancet, V2, P1488
  • [9] NORMAL MOUSE PERITONEUM CONTAINS A LARGE POPULATION OF LY-1+ (CD5) B-CELLS THAT RECOGNIZE PHOSPHATIDYL CHOLINE - RELATIONSHIP TO CELLS THAT SECRETE HEMOLYTIC ANTIBODY SPECIFIC FOR AUTOLOGOUS ERYTHROCYTES
    MERCOLINO, TJ
    ARNOLD, LW
    HAWKINS, LA
    HAUGHTON, G
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (02) : 687 - 698
  • [10] UNUSUAL PHENOTYPE OF B-CELLS IN THE THYMUS OF NORMAL MICE
    MIYAMAINABA, M
    KUMA, SI
    INABA, K
    OGATA, H
    IWAI, H
    YASUMIZU, R
    MURAMATSU, S
    STEINMAN, RM
    IKEHARA, S
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (02) : 811 - 816