Activation-induced expression of murine CD83 on T cells and identification of a specific CD83 ligand on murine B cells

被引:60
作者
Cramer, SO [1 ]
Trumpfheller, C [1 ]
Mehlhoop, U [1 ]
Moré, S [1 ]
Fleischer, B [1 ]
von Bonin, A [1 ]
机构
[1] Bernhard Nocht Inst Trop Med, D-20359 Hamburg, Germany
关键词
CD83; dendritic cells; T cell activation;
D O I
10.1093/intimm/12.9.1347
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human CD83 is a cell surface protein expressed predominantly by dendritic cells (DC) and lymphoid cells. So far, there exists no information on the function and distribution of mCD83, Here we demonstrate that mCD83 is moderately expressed on resting T cells and DC, but strongly increases In its expression on T cells following activation with antigenic peptides or T cell receptor-specific mAb. When returning to the resting state, T cells down-regulate CD83 again. Ig fusion proteins which express the extracellular part of the mCD83 molecule (mCD83-Ig) specifically inhibit antigen-specific T cell proliferation and IL-2 secretion in spleen cell cultures from DO11.10 T cell receptor transgenic mice. Staining of spleen cells from BALB/c, XID and mu MT (B cell) knockout mice with mCD83-Ig proteins reveals the presence of a CD83 ligand predominantly expressed most likely by B220(+) cells since spleen cells from mu MT knockout mice do not bind mCD83-Ig, CD83, besides its established expression on human dendritic cells, thus, also represents a new marker molecule on activated T cells which with its specific ligand is involved in the regulation of T cell responses.
引用
收藏
页码:1347 / 1351
页数:5
相关论文
共 14 条
  • [1] Immature dendritic cells phagocytose apoptotic cells via αvβ5 and CD36, and cross-present antigens to cytotoxic T lymphocytes
    Albert, ML
    Pearce, SFA
    Francisco, LM
    Sauter, B
    Roy, P
    Silverstein, RL
    Bhardwaj, N
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (07) : 1359 - 1368
  • [2] Origin, maturation and antigen presenting function of dendritic cells
    Cella, M
    Sallusto, F
    Lanzavecchia, A
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (01) : 10 - 16
  • [3] Inflammatory stimuli induce accumulation of MHC class II complexes on dendritic cells
    Cella, M
    Engering, A
    Pinet, V
    Pieters, J
    Lanzavecchia, A
    [J]. NATURE, 1997, 388 (6644) : 782 - 787
  • [4] NEW CD FROM THE B-CELL SECTION OF THE 5TH-INTERNATIONAL-WORKSHOP-ON-HUMAN-LEUKOCYTE-DIFFERENTIATION-ANTIGENS
    ENGEL, P
    TEDDER, TF
    [J]. LEUKEMIA & LYMPHOMA, 1994, 13 : 61 - 64
  • [5] PURIFICATION TO HOMOGENEITY OF B-CELL STIMULATING FACTOR - A MOLECULE THAT STIMULATES PROLIFERATION OF MULTIPLE LYMPHOKINE-DEPENDENT CELL-LINES
    GRABSTEIN, K
    EISENMAN, J
    MOCHIZUKI, D
    SHANEBECK, K
    CONLON, P
    HOPP, T
    MARCH, C
    GILLIS, S
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 163 (06) : 1405 - 1414
  • [6] PHAGE PARTICLE-MEDIATED GENE-TRANSFER TO CULTURED MAMMALIAN-CELLS
    ISHIURA, M
    HIROSE, S
    UCHIDA, T
    HAMADA, Y
    SUZUKI, Y
    OKADA, Y
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1982, 2 (06) : 607 - 616
  • [7] JENKINS MK, 1988, J IMMUNOL, V140, P3324
  • [8] DERIVATION OF A T-CELL HYBRIDOMA VARIANT DEPRIVED OF FUNCTIONAL T-CELL RECEPTOR ALPHA-CHAIN AND BETA-CHAIN TRANSCRIPTS REVEALS A NONFUNCTIONAL ALPHA-MESSENGER-RNA OF BW5147 ORIGIN
    LETOURNEUR, F
    MALISSEN, B
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1989, 19 (12) : 2269 - 2274
  • [9] Steinman RM., 2003, ANNU REV IMMUNOL, V9, P271
  • [10] The mouse Cd83 gene:: structure, domain organization, and chromosome localization
    Twist, CJ
    Beier, DR
    Disteche, CM
    Edelhoff, S
    Tedder, TF
    [J]. IMMUNOGENETICS, 1998, 48 (06) : 383 - 393