Different nuclear signals are activated by the B cell receptor during positive versus negative signaling

被引:326
作者
Healy, JI
Dolmetsch, RE
Timmerman, LA
Cyster, JG
Thomas, ML
Crabtree, GR
Lewis, RS
Goodnow, CC
机构
[1] STANFORD UNIV,SCH MED,DEPT MICROBIOL & IMMUNOL,STANFORD,CA 94305
[2] STANFORD UNIV,SCH MED,PROGRAM IMMUNOL,STANFORD,CA 94305
[3] STANFORD UNIV,SCH MED,DEPT MOL & CELLULAR PHYSIOL,STANFORD,CA 94305
[4] STANFORD UNIV,SCH MED,HOWARD HUGHES MED INST,STANFORD,CA 94305
[5] WASHINGTON UNIV,SCH MED,DEPT PATHOL,HOWARD HUGHES MED INST,ST LOUIS,MO 63110
关键词
D O I
10.1016/S1074-7613(00)80285-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It is not known how immunogenic versus tolerogenic cellular responses are signaled by receptors such as the B cell antigen receptor (BCR). Here we compare BCR signaling in naive cells that respond positively to foreign antigen and self-tolerant cells that respond negatively to self-antigen. In naive cells, foreign antigen triggered a Targe biphasic calcium response and activated nuclear signals through NF-AT, NF-kappa B, JNK, and ERK/pp90rsk. In tolerant B cells, self-antigen stimulated low calcium oscillations and activated NF-AT and ERK/pp90rsk but not NF-kappa B or JNK. Self-reactive B cells lacking the phosphatase CD45 did not exhibit calcium oscillations or ERK/pp90rsk activation, nor did they repond negatively to self-antigen. These data reveal striking biochemical differences in BCR signaling to the nucleus during positive selection by foreign antigens and negative selection by self-antigens.
引用
收藏
页码:419 / 428
页数:10
相关论文
共 69 条
  • [1] BAEUERLE PA, 1994, ANNU REV IMMUNOL, V12, P141, DOI 10.1146/annurev.immunol.12.1.141
  • [2] The NF-kappa B and I kappa B proteins: New discoveries and insights
    Baldwin, AS
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 : 649 - 683
  • [3] Immunoglobulin-mediated signal transduction in B cells from CD45-deficient mice
    Benatar, T
    Carsetti, R
    Furlonger, C
    Kamalia, N
    Mak, T
    Paige, CJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (01) : 329 - 334
  • [4] CAMBIER JC, 1994, ANNU REV IMMUNOL, V12, P457, DOI 10.1146/annurev.immunol.12.1.457
  • [5] REGULATION OF PP90RSK PHOSPHORYLATION AND S6 PHOSPHOTRANSFERASE ACTIVITY IN SWISS 3T3 CELLS BY GROWTH FACTOR-MEDIATED, PHORBOL ESTER-MEDIATED, AND CYCLIC AMP-MEDIATED SIGNAL TRANSDUCTION
    CHEN, RH
    CHUNG, JK
    BLENIS, J
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (04) : 1861 - 1867
  • [6] SPECIFIC CD45 ISOFORMS DIFFERENTIALLY REGULATE T-CELL RECEPTOR SIGNALING
    CHUI, D
    ONG, CJ
    JOHNSON, P
    TEH, HS
    MARTH, JD
    [J]. EMBO JOURNAL, 1994, 13 (04) : 798 - 807
  • [7] IDENTIFICATION OF CALCINEURIN AS A KEY SIGNALING ENZYME IN LYMPHOCYTE-T ACTIVATION
    CLIPSTONE, NA
    CRABTREE, GR
    [J]. NATURE, 1992, 357 (6380) : 695 - 697
  • [8] CLIPSTONE NA, 1994, ANNU REV BIOCHEM, V63, P1045
  • [9] IMMUNOGLOBULIN SIGNAL-TRANSDUCTION GUIDES THE SPECIFICITY OF B-CELL T-CELL-INTERACTIONS AND IS BLOCKED IN TOLERANT SELF-REACTIVE B-CELLS
    COOKE, MP
    HEATH, AW
    SHOKAT, KM
    ZENG, YJ
    FINKELMAN, FD
    LINSLEY, PS
    HOWARD, M
    GOODNOW, CC
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (02) : 425 - 438
  • [10] THE SMALL GTP-BINDING PROTEINS RAC1 AND CDC42 REGULATE THE ACTIVITY OF THE JNK/SAPK SIGNALING PATHWAY
    COSO, OA
    CHIARIELLO, M
    YU, JC
    TERAMOTO, H
    CRESPO, P
    XU, NG
    MIKI, T
    GUTKIND, JS
    [J]. CELL, 1995, 81 (07) : 1137 - 1146