The E2F-1 transcription factor promotes caspase-8 and Bid expression, and enhances Fas signaling in T cells

被引:26
作者
Cao, QY
Xia, Y
Azadniv, M
Crispe, IN
机构
[1] Univ Rochester, David H Smith Ctr Vaccine Biol & Immunol, Rochester, NY 14642 USA
[2] Univ Western Ontario, Dept Physiol & Pharmacol, London, ON N6A 3K7, Canada
关键词
D O I
10.4049/jimmunol.173.2.1111
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 immune system depends on the extensive proliferation of rare Ag-specific precursor T lymphocytes, followed by their differentiation, the delivery of,effector function, and finally death by apoptosis. T cells that lack the E2F-1 transcription factor, which is activated as cells pass the restriction point and enter S phase, show defects in activation-induced cell death. We now report that E2F-1 increases the activity of an apoptotic pathway that is important in murine primary T cells. Thus, E2F-1 promotes the transcription of Bid, a molecule that links death receptor signaling to the activation of apoptotic mechanisms in mitochondria. It also promotes the transcription of caspase-8, the enzyme that cleaves and activates Bid. Enforced expression of Bid can partially restore apoptosis in E2F-1-deficient T cells. Thus, E2F-1 integrates cell cycle progression with apoptosis.
引用
收藏
页码:1111 / 1117
页数:7
相关论文
共 45 条
  • [1] MECHANISMS OF CLASS-I RESTRICTED IMMUNOPATHOLOGY - A TRANSGENIC MOUSE MODEL OF FULMINANT-HEPATITIS
    ANDO, K
    MORIYAMA, T
    GUIDOTTI, LG
    WIRTH, S
    SCHREIBER, RD
    SCHLICHT, HJ
    HUANG, SN
    CHISARI, FV
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (05) : 1541 - 1554
  • [2] Bax and Bak: back-bone of T cell death
    Bouillet, P
    Strasser, A
    [J]. NATURE IMMUNOLOGY, 2002, 3 (10) : 893 - 894
  • [3] 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
  • [4] Mutant mouse models reveal the relative roles of E2F1 and E2F3 in vivo
    Cloud, JE
    Rogers, C
    Reza, TL
    Ziebold, U
    Stone, JR
    Picard, MH
    Caron, AM
    Bronson, RT
    Lees, JA
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (08) : 2663 - 2672
  • [5] LPR AND GLD - SINGLE GENE MODELS OF SYSTEMIC AUTOIMMUNITY AND LYMPHOPROLIFERATIVE DISEASE
    COHEN, PL
    EISENBERG, RA
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1991, 9 : 243 - 269
  • [6] Normal thymocyte negative selection in TRAIL-deficient mice
    Cretney, E
    Uldrich, AP
    Berzins, SP
    Strasser, A
    Godfrey, DI
    Smyth, MJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (03) : 491 - 496
  • [7] The genetics of the E2F family of transcription factors: shared functions and unique roles
    DeGregori, J
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2002, 1602 (02): : 131 - 150
  • [8] Transcriptional program of apoptosis induction following interleukin 2 deprivation: Identification of RC3, a calcium/calmodulin binding protein, as a novel proapoptotic factor
    Devireddy, LR
    Green, MR
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (13) : 4532 - 4541
  • [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] DIFFERENT NATURE OF THE PROLIFERATION DEFECTS OF GLD, LPR AND MEV C57BL/6 MOUSE LYMPHOID-CELLS
    FROIDEVAUX, S
    KUNTZ, L
    VELIN, D
    LOOR, F
    [J]. AUTOIMMUNITY, 1991, 10 (03) : 233 - 240