Biochemical mechanisms of IL-2-regulated Fas-mediated T cell apoptosis

被引:523
作者
Refaeli, Y
Van Parijs, L
London, CA
Tschopp, J
Abbas, AK
机构
[1] Brigham & Womens Hosp, Dept Pathol, Div Immunol Res, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] MIT, Dept Biol, Cambridge, MA 02139 USA
[4] Univ Lausanne, Inst Biochem, Lausanne Branch, CH-1066 Epalinges, Switzerland
关键词
D O I
10.1016/S1074-7613(00)80566-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
Activation-induced cell death (AICD) of lymphocytes is an important mechamism of self-tolerance. In CD4(+) T cells, AICD is mediated by the Fas pathway and is enhanced by IL-2. To define the mechanisms of this pro-apoptotic action of IL-2, we analyzed CD4(+) T cells from wild-type and IL-2(-/-) mice expressing a transgenic T cell receptor. T cells become sensitive to AICD after activation by antigen and IL-2. IL-2 increases transcription and surface expression of Fas ligand (FasL) and suppresses transcription and expression of FLIP, the inhibitor of apoptosis. The ability of IL-2 to enhance expression of a pro-apoptotic molecule, Fast, and to suppress an inhibitor of Fas signaling, FLIP, likely accounts for the role of this cytokine in potentiating T cell apoptosis.
引用
收藏
页码:615 / 623
页数:9
相关论文
共 40 条
  • [1] Bcl-x(L) can inhibit apoptosis in cells that have undergone Fas-induced protease activation
    Boise, LH
    Thompson, CB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) : 3759 - 3764
  • [2] A NOVEL PROTEIN THAT INTERACTS WITH THE DEATH DOMAIN OF FAS/APO1 CONTAINS A SEQUENCE MOTIF RELATED TO THE DEATH DOMAIN
    BOLDIN, MP
    VARFOLOMEEV, EE
    PANCER, Z
    METT, IL
    CAMONIS, JH
    WALLACH, D
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (14) : 7795 - 7798
  • [3] Involvement of MACH, a novel MORT1/FADD-interacting protease, in Fas/APO-1- and TNF receptor-induced cell death
    Boldin, MP
    Goncharov, TM
    Goltsev, YV
    Wallach, D
    [J]. CELL, 1996, 85 (06) : 803 - 815
  • [4] CELL-AUTONOMOUS FAS (CD95) FAS-LIGAND INTERACTION MEDIATES ACTIVATION-INDUCED APOPTOSIS IN T-CELL HYBRIDOMAS
    BRUNNER, T
    MOGIL, RJ
    LAFACE, D
    YOO, NJ
    MAHBOUBI, A
    ECHEVERRI, F
    MARTIN, SJ
    FORCE, WR
    LYNCH, DH
    WARE, CF
    GREEN, DR
    [J]. NATURE, 1995, 373 (6513) : 441 - 444
  • [5] FADD, A NOVEL DEATH DOMAIN-CONTAINING PROTEIN, INTERACTS WITH THE DEATH DOMAIN OF FAS AND INITIATES APOPTOSIS
    CHINNAIYAN, AM
    OROURKE, K
    TEWARI, M
    DIXIT, VM
    [J]. CELL, 1995, 81 (04) : 505 - 512
  • [6] Interaction of CED-4 with CED-3 and CED-9: A molecular framework for cell death
    Chinnaiyan, AM
    ORourke, K
    Lane, BR
    Dixit, VM
    [J]. SCIENCE, 1997, 275 (5303) : 1122 - 1126
  • [7] Qualitative and quantitative contributions of the T cell receptor zeta chain to mature T cell apoptosis
    Combadiere, B
    Freedman, M
    Chen, L
    Shores, EW
    Love, P
    Lenardo, MJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) : 2109 - 2117
  • [8] AUTOCRINE T-CELL SUICIDE MEDIATED BY APO-1/(FAS/CD95)
    DHEIN, J
    WALCZAK, H
    BAUMLER, C
    DEBATIN, KM
    KRAMMER, PH
    [J]. NATURE, 1995, 373 (6513) : 438 - 441
  • [9] DOMINANT INTERFERING FAS GENE-MUTATIONS IMPAIR APOPTOSIS IN A HUMAN AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME
    FISHER, GH
    ROSENBERG, FJ
    STRAUS, SE
    DALE, JK
    MIDDELTON, LA
    LIN, AY
    STROBER, W
    LENARDO, MJ
    PUCK, JM
    [J]. CELL, 1995, 81 (06) : 935 - 946
  • [10] Fournel S, 1996, J IMMUNOL, V157, P4309